We would like to thank Dr. Elif Kamber-Kaya for her help to establish the protocol in the lab. Dr. Guy Salvesen kindly provided the DriceC211A mutant9. This work was funded by a MIRA award from the National Institute of General Medical Sciences (NIGMS) of the National Institutes of Health (NIH) under grant number 2R35GM118330. The funders had no role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript.

1. Recombinant caspase expression in bacteria
<ol>
	<li>Clone the gene of interest (Caspase or putative substrate) into a bacterial expression vector with N- and/or C-terminal tag(s) using standard protocols23. 
	NOTE: Tags can increase the solubility of the recombinant proteins and are used for purification of the recombinant proteins. Here, Dronc, Drice, and their catalytic mutants are cloned into the vector pET28a, which provides an N-terminal 6xHis tag (pET28a-6xHis-Droncwt, pET28a-6xHis-DroncC318A, pET28a-6xHis-Dricewt, pET28a-6xHis-DriceC211A); (for primer information see Supplementary Table 1).</li>
	<li>Transform the vectors with the genes of interest into competent BL21 (DE3) pLysS E. coli cells using standard procedures23,24. Plate the transformation mixture on LB agar plates with the appropriate antibiotic (kanamycin in case of pET28a) to select transformed bacteria. (Refer to Supplementary Table 2.)</li>
	<li>Pick a colony from the plate and inoculate in 5 mL of LB medium containing the appropriate antibiotic to grow overnight at 37 &#730;C at 220 rpm on a shaking platform.</li>
	<li>On the next day, prepare 30-50 mL (per sample) of LB medium with antibiotic and add 1 mL of the overnight grown culture. The optical density at 600 nm (OD600) using a bio photometer/spectrophotometer should be between 0.1 and 0.2.</li>
	<li>Grow the culture at 37 &#730;C at 220 rpm on a shaking platform until OD600 reaches 0.6. Check the OD600 every hour until it reaches 0.6. This takes about 2 to 3 h.</li>
	<li>To induce protein (caspase) expression, add IPTG to a final concentration of 0.1-0.2 mM (dilute 1:1,000-1:500 from IPTG stock, see Supplementary Table 2).</li>
	<li>Grow the cultures for 3 h at 30 &#730;C at 220 rpm. 
	NOTE: Time and temperature are dependent on what kind of protein is being expressed and its solubility. These conditions may need to be adjusted if different caspases or substrates are expressed.</li>
	<li>After 3 h, spin down the cultures in 50 mL centrifuge tubes for 20 min at 4 &#730;C at 2,000 x g. Discard the supernatant and proceed with the pellet. 
	&#8203;NOTE: The protocol can be stopped at this point and continued later. Bacterial pellets can be frozen at -80 &#730;C.</li>
</ol>
2. Small-scale recombinant caspases extraction
<ol>
	<li>Remove the frozen tubes with the pelleted cultures from -80 &#730;C storage and keep them on ice for 10 min to soften the pellet.</li>
	<li>After 10 min, add 0.6 mL of bacterial cell lysis buffer (Supplementary Table 2) supplemented with freshly added protease inhibitors, 10 mg/mL of lysozyme and 50 U/mL of benzonase into the pellet-containing tubes using a pipette controller with a 1 mL serological pipette.</li>
	<li>With the same pipette tip, dissolve the pellet by pipetting up and down until a clear pale-yellow solution without any pellet particles is visible. Incubate for 30 min on ice.</li>
	<li>Transfer the lysate into appropriate centrifuge tubes and centrifuge the lysates at 17,000 x g for 40 min at 4 &#730;C.</li>
	<li>Transfer the supernatants into a 1.5 mL microcentrifuge tube. This is the crude extract containing the caspases.</li>
	<li>Keep the tubes on ice and proceed for purification with Ni-NTA agarose.</li>
</ol>
3. Small-scale His-tagged caspases purification
<ol>
	<li>Add 0.2 mL of the 50% slurry of Ni-NTA agarose to each tube of the caspase extracts from step 2.5. Rotate the tubes on an end-on-end rotator for 1 h at 4 &#730;C.</li>
	<li>After 1 h, add the extract with the Ni-NTA agarose to 1 mL polypropylene columns with the tip intact, placed in a rack. Let it stand for 5 min.</li>
	<li>After 5 min, remove the cap of the columns and let the supernatant flow out by gravity flow.</li>
	<li>Carefully add 1 mL of the wash buffer (Supplementary Table 2) to the columns without disturbing the packed resin of Ni-NTA agarose and wash it through gravity flow.</li>
	<li>Perform the washing step three times.</li>
	<li>For elution of the caspases, place 1.5 mL microcentrifuge tubes under the collecting nozzle of the columns after complete draining of the wash buffer.</li>
	<li>Add 0.5 mL of the elution buffer (supplemented with 1x protease inhibitors immediately before use) to each column and collect the eluate in the 1.5 mL microcentrifuge tubes. 
	NOTE: The fine purified eluate will be transparent in color.</li>
	<li>Keep the eluates on ice and measure the concentration of proteins by Bradford assay25. Confirm purity/homogeneity of the purified caspases by SDS-PAGE followed by Coomassie Blue staining26. 
	&#8203;NOTE: The yield of a 50 mL LB culture ranges between 0.5 and 1.5 mg of caspase protein. Given that 0.5 mL of elution buffer is used for elution, the concentration ranges from 1 to 3 mg/mL. It is important to use the purified caspase eluates for in vitro cleavage assays on the same day of lysis and purification as these caspase preparations lose activity over night.</li>
</ol>
4. Expression of the putative caspase substrate in cell-free expression systems
NOTE: In this protocol, Drice, the natural substrate of Dronc, is prepared by both recombinant expression in E. coli (see section 3 above) and by expression in rabbit reticulocyte lysate (RRL), a mammalian cell-free expression system (this section, see below).
<ol>
	<li>Clone the gene of the putative substrate into an expression vector containing either a T7, T3, or SP6 promoter using standard procedures23. 
	NOTE: In this protocol, DriceC211A is being used as the model substrate and was cloned into the vector pT7CFE1-N-Myc, which carries a T7 promoter for gene expression and tags the putative protein substrate with an N-terminal Myc-tag for detection by immunoblotting.</li>
	<li>In RRL, candidate substrates can be synthesized either radioactively or non-radioactively.
	<ol>
		<li>Non-radioactive synthesis: In a 0.5 mL microcentrifuge tube, add 25 &#181;L of RRL, 2 &#181;L of reaction buffer, 0.5 &#181;L of Amino Acid Mixture -Minus Leucine (1 mM), 0.5 &#181;L of Amino Acid Mixture-Minus Methionine (1 mM), 1 &#181;L of Ribonuclease Inhibitor (40 U/&#181;L), 2 &#181;L of DNA Template (0.5 &#181;g/&#181;L), and 1 &#181;L of T7-RNA Polymerase. Add nuclease-free water to adjust the final volume of the reaction to 50 &#181;L. Gently mix the components by pipetting or stirring with pipette tip, and spin down briefly. 
		NOTE: The RRL lysate contains 100-200 mg/mL of the endogenous proteins. For in vitro translation reactions, add the RRL at 50% concentration (here 25 &#181;L/50 &#181;L reaction).</li>
		<li>Radioactive synthesis: In a 0.5 mL microcentrifuge tube, add 25 &#181;L of RRL lysate, 2 &#181;L of reaction buffer, 0.5 &#181;L of Amino Acid Mixture-Minus Methionine (1 mM), 1 &#181;L of Ribonuclease Inhibitor (40 U/&#181;L), 2 &#181;L of DNA Template (0.5 &#181;g/&#181;L), 2 &#181;L of S35-labeled Methionine (1000 Ci/mmol at 10 mCi/mL) and 1 &#181;L of T7-RNA Polymerase. Add nuclease-free water to adjust the final volume of the reaction to 50 &#181;L. Gently mix the components by pipetting or stirring with pipette tip, and spin down briefly. Dispose of tips and tubes in a radioactive waste container. 
		NOTE: Do not add the Amino Acid Mixture without Leucine. The pT7CFE1 vector uses a T7 promoter for protein expression. Other vectors use T3 or SP6 promoters. In that case, T3 or SP6 RNA polymerases should be used instead of T7 RNA polymerase. Please make sure that the DNA template is of high purity.</li>
	</ol>
	</li>
	<li>Incubate the reaction at 30 &#730;C for 90 min.</li>
	<li>Spin briefly for 10 s and place the tubes on ice. Check the expression level of the putative substrate in RRL by SDS-PAGE and immunoblotting/autoradiography. 
	&#8203;NOTE: The amount of RRL extract added to the cleavage reaction should be based on the amount of protein that can be detected by the detection method (either immunoblotting or S35 autoradiography). Proceed to the in vitro cleavage assay (next section) or store it at -80 &#730;C.</li>
</ol>
5. In vitro cleavage assay with substrates generated with RRL
<ol>
	<li>Take the putative substrate(s) generated, as described in section 4. In this protocol, N-Myc-DriceC211A is used as model substrate.</li>
	<li>Depending on the expression level of the putative substrate (to be determined separately by immunoblot or autoradiography analysis, see step 4.4), use 1-10 &#181;L of the RRL programmed with the protein of interest in the cleavage assay.</li>
	<li>Add 10 &#181;g of purified caspase protein generated in sections 1, 2, and 3.</li>
	<li>Bring the total reaction volume to 50 &#181;L with caspase assay buffer.</li>
	<li>Incubate the reactions in a water bath at 30 &#730;C for 3 h. Make sure to include the appropriate controls in the cleavage assay. Here, the catalytic mutant DroncC318A is used as control.</li>
	<li>After 3 h, stop the reactions by transferring the tubes on ice.</li>
	<li>Add one volume of LDS sample buffer containing 50 mM DTT. The reaction is stopped completely with the addition of LDS sample buffer.</li>
	<li>Incubate the samples at 75 &#730;C in a heat block for 10 min.</li>
	<li>Quickly spin, mix by flicking, load 24 &#181;L per sample and run the SDS-PAGE (see section 7) or store the samples at -20 &#730;C.</li>
</ol>
6. In vitro cleavage assay with bacterially expressed recombinant substrate protein
<ol>
	<li>Add 10 &#181;g of purified candidate substrate (here 6xHis-DriceC211A, generated in sections 1, 2, and 3) to a 0.5 mL microcentrifuge tube.</li>
	<li>Add 10 &#181;g of the purified caspase proteins generated in sections 1 and 2. Bring the total volume to 50 &#181;L by using caspase assay buffer.</li>
	<li>Follow steps 5.5 to 5.9.</li>
</ol>
7. SDS-PAGE and immunoblotting
<ol>
	<li>Load the cleavage reactions (24 &#181;L) onto 4%-12% Tris-Glycine or Bis-Tris gradient gels (Table of Materials) and perform protein electrophoresis and immunoblotting (or autoradiography if using S35-labeled substrates) to visualize results using standard procedures27,28. 
	NOTE: Here, in this protocol, Bis-Tris gradient gels with Mops running buffer and LDS loading buffer were used. In general, the commonly used PAGE protocols of Tris-Glycine gels run using the Tris-Glycine-SDS running buffer and the SDS-loading buffer work well.</li>
</ol>

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L., Gershon, P. D., Cramer, K. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Non-Apoptotic+caspase+activity+preferentially+targets+a+novel+consensus+sequence+associated+with+cytoskeletal+proteins+in+the+developing+auditory+brainstem.">Non-Apoptotic caspase activity preferentially targets a novel consensus sequence associated with cytoskeletal proteins in the developing auditory brainstem.</a> Frontiers in Cell and Developmental Biology. 10, 844844 (2022).</li></ol>

The authors declare no competing interests.

The bulk of our knowledge about caspases and caspase function has been derived from intense work in apoptosis during the last three decades. It is very well established that initiator caspases proteolytically process effector caspases, and hundreds of proteins have been identified as effector caspase substrates during apoptosis5,29. In contrast, much less is known about the function of caspases for non-apoptotic processes and which non-apoptotic substrates they are processing. It is conceivable that initiator caspases are key decision makers here. During apoptosis, they activate effector caspases causing cell death. However, to trigger non-apoptotic processes, they may activate different proteins (other than effector caspases), which control the non-apoptotic process. This protocol tests candidate proteins as substrates of the initiator caspase Dronc in Drosophila17,30.
The substrates to be tested in the cleavage assay can be produced either in an in vitro mammalian cell-free expression system such as RRL or by recombinant expression in E. coli. There are several advantages for in vitro expression using RRL over bacterial expression. The RRL expression protocol is simple and fast, allowing many different substrates to be prepared in parallel. In many cases, the RRL extract containing the protein of interest can be stored at -80 &#730;C before use in the cleavage assay (although this needs to be determined separately for each substrate). The putative substrate can be labeled with S35-Met, which allows easy analysis by autoradiography after SDS-PAGE. That is particularly useful, if no substrate-specific antibody is available. Alternatively, if S35-Met labeling is not desired, the putative substrate can be tagged with common tags such as Flag, HA, or Myc tags, which allows detection of caspase cleavage by immunoblotting.
It needs to be strongly emphasized that the success of this protocol depends on the careful and consistent purification of the recombinant Dronc and Drice proteins. Unfortunately, these proteins cannot be stored &#8212; not even short-term&#160;&#8212;&#160;neither in the fridge nor frozen. They lose the enzymatic activity overnight in any stored form. Therefore, they need to be prepared freshly on the day of the cleavage assay. Regardless of the candidate protein(s) being tested, DriceC211A should always be used as a positive control to validate the enzymatic activity of the Droncwt preparation (see Figure 2B,C). Alternatively, the activity of the Dronc and Drice preparations can also be tested by in vitro cleavage of fluorogenic synthetic tetrapeptide substrates2,9,31.
If antibodies are used to detect the candidate substrates, they need to be validated by the user32,33. That applies also to commercially available antibodies that detect epitope tags such as Flag, HA, Myc, or others. Poor antibody quality can obscure important results. Double-epitope-tagging of the candidate substrates on both the N- and C-terminus with different tags is also recommended34. If cleavage occurs, double tagging helps to trace both cleavage products and may help to elucidate if cleavage occurs at one or more sites.
While this protocol easily validates the known biological substrate of Dronc, Drice, there are also limitations. One limitation is that this is an in vitro protocol with recombinant proteins. In these assays, the caspases are present at an unphysiologically high concentration, which is evident from the observation that they can spontaneously auto-process in E. coli. The spontaneous auto-processing usually does not occur under the physiological conditions. This high caspase concentration may cause spurious activity resulting in false positives. False positives can be eliminated by lowering the caspase concentration in the in vitro cleavage reaction. Furthermore, as outlined in more detail below, additional assays are necessary to confirm genuine substrates and to eliminate false positives.
The recombinant caspases may not have the same specificity as they have in their normal cellular environment in vivo. For example, the activity of caspases can be modified by post-translational modifications. These are not present on the recombinant proteins. Furthermore, in vivo, initiator caspases, including Dronc are incorporated into large protein complexes such as the apoptosome. Under the conditions of this protocol, formation of the apoptosome is not achieved. That would require recombinant expression of Drosophila Apaf-1 (aka Dark or Hac-1)35-37 which has challenges of its own. Therefore, in vitro, Dronc may not have the same specificity that it has in vivo.
It is also conceivable that Dronc is incorporated into a different protein complex for non-apoptotic processes. This may confer a different cleavage specificity to Dronc, which could also explain why Dronc does not induce apoptosis under non-apoptotic conditions. Related to this, CasCleave uses the known cleavage consensus sites to predict new caspase substrates. However, it is unknown whether the same cleavage consensus sites are also used for non-apoptotic processes. In fact, recently, it was shown that Caspase-3 changes its preferred consensus site during a non-apoptotic process in the developing auditory brainstem in the chick embryo38. Likewise, if initiator caspases are incorporated into different protein complexes, they may have a different specificity and thus may cleave at different consensus sequences.
These limitations illustrate that it is not sufficient to solely rely on the in vitro cleavage assays described in this protocol. Alternative approaches should be employed to further validate the results obtained using this protocol. Ideally, in vivo assays should be used to address the following questions: Is the candidate protein proteolytically processed during the non-apoptotic process in vivo? If so, is the same cleavage site used in vivo and in vitro? What is the consequence if the cleavage is blocked by mutagenesis of the cleavage site? Is the processing of the candidate substrate dependent on caspases, and if so, which one? What is the role of the cleavage fragments for the non-apoptotic process? These questions can be easily addressed in the genetic model organisms such as C. elegans and Drosophila using standard genetic and transgenic methods.
In summary, this protocol describes a reliable and consistent method to produce enzymatically active caspases, specifically the Drosophila caspases Dronc and Drice. The ultimate goal of this protocol is to examine whether Dronc can cleave candidate substrates in vitro, which were identified by genetic, biochemical, or bioinformatics approaches. As explained in the previous paragraph, additional assays are required to validate these proteins as caspase substrates in vivo. Given the degree of conservation of caspase genes across metazoa, it should be possible to adapt this protocol to caspases from other organisms as well.

Programmed cell death or apoptosis is executed by a class of highly specialized cell death proteases termed caspases (reviewed in reference1). Caspases are Cys proteases that contain a Cys residue in the catalytic site. They have defined consensus cleavage sites and cleave substrates proteolytically after Asp residues (although the Drosophila caspase Dronc has also been reported to cleave after Glu residues2). They are subdivided into initiator (also known as apical or upstream) and effector (executioner or downstream) caspases. Initiator caspases activate effector caspases. For example, in mammals, the initiator caspase Caspase-9 cleaves and activates the effector caspase Caspase-33. Likewise, in Drosophila melanogaster, the caspase-9-ortholog Dronc cleaves and activates the caspase-3-ortholog Drice2,4. During apoptosis, effector caspases cleave hundreds of substrates leading to the death of the cell5.
Caspases are synthesized as inactive proenzymes (zymogens) in the cell. In this form, they contain an N-terminal prodomain, a large subunit with the catalytic Cys in the central portion of the proenzyme, and a small subunit at the C-terminus1 (Figure 1). The mechanism of activation is different between initiator and effector caspases. Initiator caspases (Caspase-9, Dronc) require dimerization for activation, which occurs by incorporation into a large protein complex, termed the apoptosome6. For the incorporation into the apoptosome, Caspase-9 and Dronc carry a caspase activation and recruitment domain (CARD) in the N-terminal prodomain (Figure 1). The apoptosome component Apaf-1 also contains a CARD and recruits Caspase-9 or Dronc via CARD/CARD interaction into the apoptosome3,6,7. While Caspase-9 and Dronc can be proteolytically processed in the apoptosome, this processing is not fully required for enzymatic activity8,9.
In contrast, effector caspases (Caspase-3, Drice) do not carry a CARD in their prodomains and are not incorporated into large protein complexes for activation1. They are dependent on proteolytic cleavage by active Caspase-9 or Dronc1, respectively. The active effector caspase forms a tetramer composed of two large and two small subunits, and thus contains two catalytic sites (Figure 1). Importantly for this protocol, recombinant expression of caspases in E. coli causes auto-processing and activation of caspases, including Drice10 and Dronc2,8,9,11,12, even in the absence of Apaf-1. This auto-processing allows to perform in vitro cleavage assays of candidate substrates with recombinant caspase protein.
Caspases are not only involved in apoptosis, but they can also have many non-apoptotic functions, including proliferation, differentiation, cell migration, neuronal pruning, innate immunity, and others13,14,15. It is currently unknown how cells can survive despite containing active caspases during non-apoptotic processes. It is possible that these cells activate caspases only at sub-lethal levels16 or they sequester active caspases in non-apoptotic compartments of the cell such as the plasma membrane17,18. Therefore, the identification and verification of non-apoptotic substrates will not only reveal how caspases mediate non-apoptotic processes but may also help to understand how cells can survive in the presence of active caspases.
Candidate proteins as caspase substrates can be identified using genetic and biochemical methods. Identified proteins can be checked for the presence of the consensus Dronc cleavage sites. This can be done by visually inspecting the protein sequence&#160;or using more sophisticated online bioinformatic tools such as CasCleave (https://sunflower.kuicr.kyoto-u.ac.jp/~sjn/Cascleave/)19,20. These tools use the known consensus cleavage sites of caspases and structural considerations to predict novel targets of caspases. While CasCleave incorporates the information of verified substrates from human Caspases-1, -3, -6, -7, and -8, it may nevertheless also be useful for the purposes described here as these caspases and their consensus cleavage sites are well conserved. However, because the Dronc cleavage site is not well defined (two studies identified two different optimal cleavage sites, TATD/E2 and LALD9), the candidate substrates are also examined for the presence of other caspase cleavage site, including Drice.
To validate the predicted substrates of caspases, additional assays are necessary. One of these assays is the demonstration that a given caspase can actually cleave the candidate protein in vitro. Here, we provide a convenient protocol for in vitro caspase cleavage assays. Using this protocol, candidate substrates are tested with Dronc as the caspase. They can also be tested as substrates of Drice. Although this protocol is written for the Drosophila caspases Dronc and Drice, it can also be adapted for caspases from other organisms.
The extraction and purification of Dronc and Drice along with the in vitro cleavage assay must be performed on the same day due to the loss of catalytic activity by these caspases. This protocol has been modified and optimized from previous publications8,9,11,12,21,22. In this protocol, four different caspase proteins are recombinantly expressed in the E. coli strain BL21 (DE3) pLysS. These proteins are: 6xHis-Droncwt, 6xHis-DroncC318A, 6xHis-Dricewt, and 6xHis-DriceC211A. Each of these proteins is tagged with 6 Histidine residues (6xHis) at the N-terminus for purification. Droncwt and Dricewt are the wild-type proteins and can auto-process into the active caspase upon recombinant expression. DroncC318A and DriceC211A encode mutant forms of Dronc and Drice that change the catalytic Cys residue to an Ala residue. These constructs are catalytically inactive and cannot auto-process (see Figure 2A). They are used as controls in the cleavage assay. Because DriceC211A cannot auto-process, it is also used as the model substrate for Droncwt in the in vitro cleavage assay described here.

<table><tbody><tr><td>Ampicillin</td><td>Fisher</td><td>BP1760-25</td><td></td></tr><tr><td>Anti-His antibody</td><td>Sigma-Aldrich</td><td>MA1-21315</td><td></td></tr><tr><td>Anti-mouse IgG, HRP-linked Antibody</td><td>Cell signaling</td><td>7076P2</td><td></td></tr><tr><td>Anti-Myc antibody</td><td>Santa Cruz Biotechnology</td><td>sc-40</td><td></td></tr><tr><td>Anti-rabbit IgG, HRP-linked Antibody</td><td>Cell signaling</td><td>7074P2</td><td></td></tr><tr><td>Benchtop Centrifuge</td><td>Eppendorf</td><td>5415 R</td><td></td></tr><tr><td>Benzonase</td><td>Sigma-Aldrich</td><td>E1014-5KU</td><td></td></tr><tr><td>BioPhotometer</td><td>Eppendorf</td><td>#6131</td><td></td></tr><tr><td>BL21 (DE3) pLysS Competent Cells</td><td>Promega</td><td>L1195</td><td></td></tr><tr><td>Centrifuge rotor</td><td>Beckman Coulter</td><td>JA-25.50</td><td></td></tr><tr><td>CHAPS&amp;nbsp;</td><td>Sigma-Aldrich</td><td>C3023-1G</td><td></td></tr><tr><td>ChemiDoc with image software</td><td>Bio-Rad</td><td>Universal Hood II</td><td>For Chemiluminiscence imaging</td></tr><tr><td>Chemiluminiscence Substrate</td><td>Thermofisher Scientific</td><td>34095</td><td>For Chemiluminiscence imaging</td></tr><tr><td>Cleaved Drosophila ICE (drICE) (Asp230) Antibody</td><td>Cell Signaling Technology</td><td>9478S</td><td></td></tr><tr><td>Disposable cuvettes</td><td>Fisher Scientific</td><td>14955128</td><td>Used to measure bacterial growth and protein concentration</td></tr><tr><td>Dithiothreitol (DTT)</td><td>Bio-Rad</td><td>#1610610</td><td></td></tr><tr><td>Erlenmeyer flasks, 1000 mL</td><td>Millipore sigma</td><td>CLS49801L</td><td>For LB agar media preparation and autoclaving</td></tr><tr><td>Erlenmeyer flasks, 250 mL</td><td>Millipore sigma</td><td>CLS4980250</td><td>For bacterial culture growth and induction.</td></tr><tr><td>Ethylene-diamine-tetra-acetic Acid (EDTA)</td><td>Sigma-Aldrich</td><td>E5134</td><td></td></tr><tr><td>Gel extraction kit</td><td>Qiagen</td><td>28704</td><td></td></tr><tr><td>Gel tank SDS-PAGE system</td><td>Thermofisher Scientific</td><td>STM1001</td><td></td></tr><tr><td>Glycine</td><td>Sigma-Aldrich</td><td>G8898</td><td></td></tr><tr><td>Halt Protease Inhibitor Cocktail (100x)</td><td>Thermofisher scientific</td><td>87786</td><td></td></tr><tr><td>HEPES</td><td>Sigma-Aldrich</td><td>H3375</td><td></td></tr><tr><td>His-Drice-pET28a&amp;nbsp;</td><td>This study</td><td>N/A</td><td>Available from authors</td></tr><tr><td>His-DriceC211A-pET28a&amp;nbsp;</td><td>This study</td><td>N/A</td><td>Available from authors</td></tr><tr><td>His-Dronc-pET28a&amp;nbsp;</td><td>This study</td><td>N/A</td><td>Available from authors</td></tr><tr><td>His-DroncC318A-pET28a&amp;nbsp;</td><td>This study</td><td>N/A</td><td>Available from authors</td></tr><tr><td>Imidazole</td><td>Sigma-Aldrich</td><td>I2399-100G</td><td></td></tr><tr><td>Isopropyl-&amp;szlig;-D-thiogalactopyranoside (IPTG)</td><td>Thermofisher Scientific</td><td>FERR0392</td><td></td></tr><tr><td>Kanamycin</td><td>Fisher Scientific</td><td>BP906-5</td><td></td></tr><tr><td>LB Agar, Miller (Powder)</td><td>Fisher Scientific</td><td>BP1425-500</td><td></td></tr><tr><td>LB Broth, Miller</td><td>Fisher Scientific</td><td>BP1426-500</td><td></td></tr><tr><td>Lysozyme</td><td>Thermofisher Scientific</td><td>90082</td><td></td></tr><tr><td>Microbiological plate incubator</td><td>Fisher Scientific</td><td>11-690-650D</td><td>For colony growth after transformation</td></tr><tr><td>Microcentrifuge tubes, 0.5 mL</td><td>Eppendorf</td><td>22363611</td><td></td></tr><tr><td>Microcentrifuge tubes, 1.5 mL</td><td>Eppendorf</td><td>22363204</td><td></td></tr><tr><td>Midiprep kit</td><td>Qiagen</td><td>12243</td><td></td></tr><tr><td>Mini tube rotator</td><td>Fisher Scientific</td><td>05-450-127</td><td>for mixing bacterial lysates and Ni-NTA agarose</td></tr><tr><td>Miniprep kit</td><td>Qiagen</td><td>27106</td><td></td></tr><tr><td>Motorized Pipette Controller</td><td>Gilson</td><td>F110120</td><td>For using serological pipettes</td></tr><tr><td>NaH2PO4</td><td>Fisher Scientific</td><td>BP330-1</td><td></td></tr><tr><td>Ni-NTA Agarose</td><td>Qiagen</td><td>30210</td><td></td></tr><tr><td>NuPAGE 4 to 12%, Bis-Tris, 1.0 mm, Midi Protein Gel, 20-well</td><td>Thermofisher Scientific</td><td>WG1402BOX</td><td></td></tr><tr><td>NuPAGE LDS Sample Buffer (4x)</td><td>Thermofisher Scientific</td><td>NP0007</td><td></td></tr><tr><td>NuPAGE MOPS SDS Running Buffer (20x)</td><td>Thermofisher Scientific</td><td>NP0001</td><td></td></tr><tr><td>NuPAGE Transfer Buffer (20x)</td><td>Invitrogen</td><td>NP00061</td><td></td></tr><tr><td>Orbital shaking incubator with temperature control</td><td>New Brunswick Scientific</td><td>C25 incubator shaker</td><td></td></tr><tr><td>Petridish 100 mm x 15 mm</td><td>Fisher Scientific</td><td>FB0875712</td><td></td></tr><tr><td>Plating beads</td><td>Zymo research</td><td>S1001</td><td>For spreading culture on AmpR/KanR plates</td></tr><tr><td>Polypropylene Columns (1 mL)</td><td>Qiagen</td><td>34924</td><td>For purification of His-tagged proteins</td></tr><tr><td>Precision Plus Protein Standards</td><td>Bio-Rad</td><td>#161-0374</td><td></td></tr><tr><td>Protein Assay Dye Reagent Concentrate</td><td>Bio-Rad</td><td>#5000006</td><td></td></tr><tr><td>pT7CFE1-NMyc</td><td>Thermofisher Scientific</td><td>88863</td><td>For cloning substrates for RRL expression</td></tr><tr><td>PVDF membrane</td><td>Invitrogen</td><td>LC2007</td><td></td></tr><tr><td>14 mL Polypropylene round bottom tubes</td><td>Fisher Scientific</td><td>352029</td><td>For growing plasmid cultures</td></tr><tr><td>QiaRack</td><td>Qiagen</td><td>19095</td><td>For holding polypropylene columns during purification</td></tr><tr><td>Refrigerated High speed Centrifuge</td><td>Beckman Coulter</td><td>Avanti J-25</td><td></td></tr><tr><td>rRNasin Ribonuclease Inhibitor</td><td>Promega</td><td>N251A</td><td>For RRL expression</td></tr><tr><td>Sodium chloride</td><td>Fisher Scientific</td><td>BP358-212</td><td></td></tr><tr><td>Sodium Hydroxide</td><td>Fisher Scientific</td><td>BP359-500</td><td></td></tr><tr><td>Sterile Falcon tubes, 15 mL</td><td>Fisher Scientific</td><td>05-527-90</td><td></td></tr><tr><td>Sterile Falcon tubes, 50 mL</td><td>Fisher Scientific</td><td>14-959-49A</td><td></td></tr><tr><td>Sucrose</td><td>Sigma-Aldrich</td><td>S70903-250G</td><td></td></tr><tr><td>1 mL Serological Pipets, Sterile</td><td>celltreat</td><td>229001B</td><td>For bacterial cell lysis in 50 mL tubes</td></tr><tr><td>TnT Coupled Reticulocyte Lysate -T7</td><td>Promega</td><td>L4611</td><td></td></tr><tr><td>Tris-base</td><td>Fisher Scientific</td><td>BP154-1</td><td></td></tr><tr><td>Tween 20</td><td>Sigma-Aldrich</td><td>P1379</td><td></td></tr><tr><td>Waterbath</td><td>Fisher Scientific</td><td>2340</td><td></td></tr><tr><td>Western wet transferring cassette</td><td>Thermofisher Scientific</td><td>STM2001</td><td></td></tr></tbody></table>

in vitro cleavage assays using purified recombinant drosophila caspases for substrate screening

Caspases are very specific cell death proteases that are involved in apoptotic and non-apoptotic processes. While the role of caspases during apoptosis has been very well defined and many apoptotic proteolytic substrates of caspases have been identified and characterized, the role of caspases for non-apoptotic processes is not well understood. In particular, few non-apoptotic substrates of caspases have been identified thus far. Here, in order to facilitate the identification and characterization of potential caspase substrates, a protocol that allows the testing of candidate substrates in caspase cleavage assays in vitro is described. This protocol includes the production and purification of recombinant caspase proteins, the production of the candidate substrates either recombinantly or in a cell-free expression system, and the actual in vitro cleavage reaction followed by SDS-PAGE and immunoblotting. This protocol is tailored for the Drosophila caspases Dronc and Drice but can easily be adapted for caspases from other organisms, including mammals.

This protocol provides step-by-step instructions for the caspase protein induction in E. coli, purification of the recombinant Drosophila caspases Dronc and Drice, the synthesis of candidate substrates, and the in vitro cleavage reaction with candidate substrates (here DriceC211A) and the caspase Dronc. The catalytic mutant DriceC211A was used as model substrate in this assay because it does not have auto-processing activity (Figure 2A) and remains full-length until it is cleaved by Droncwt. DriceC211A should always be used as a positive control to validate that the Droncwt preparation has enzymatic activity.
Figure 2A provides a representative example of the expression and purification of recombinant caspases. Four different recombinant caspases were induced and purified: 6xHis-Droncwt, 6xHis-DroncC318A, 6xHis-Dricewt, and 6xHis-DriceC211A. The purified caspases were run by SDS-PAGE, immunoblotted, and the blot was probed with an anti-His antibody (diluted 1:5,000; followed by anti-mouse IgG, HRP-linked antibody (1:10,000)). The unprocessed 6xHis-Dronc (proDronc) runs at a relative molecular weight (MWr) of 55 kDa (lane 2) and unprocessed 6xHis-Drice (proDrice) has a MWr of 35 kDa (lane 4). Auto-processing of the caspases is visible by the appearance of bands of smaller MWr which due to the presence of the His-tag at the N-terminus represent the large subunits of the caspases (Figure 1). In the case of 6x-Dronc, the large subunit has a MWr of 40 kDa (lane 1). The large subunit of 6x-Drice runs at 23 kDa (lane 3). The catalytic mutants 6xHis-DroncC318A and 6xHis-DriceC211A fail to auto-process and are only detectable as full-length proteins (lanes 2 and 4).
Figure 2B To demonstrate that the bacterially produced and purified 6xHis-Droncwt preparation has enzymatic activity, an in vitro cleavage assay as described in this protocol was performed. As negative control, the catalytic mutant 6xHis-DroncC318A was used. The substrate was RRL-generated N-Myc-DriceC211A, which is tagged with a Myc-tag at the N-terminus. After the in vitro cleavage reaction, the proteins were separated by SDS-PAGE, immunoblotted and the blots were incubated with an anti-Myc antibody (diluted 1:1,000) followed by anti-mouse IgG, HRP-linked antibody (1:10,000)) to detect N-Myc-DriceC211A. Successful cleavage and thus enzymatic activity of the caspase can be demonstrated by the appearance of at least one band of smaller MWr compared to the full-length, unprocessed form of the substrate. Unprocessed, full-length N-Myc-DriceC211A has a MWr of 40 kDa (lanes 2 and 4), whereas the large subunit of processed N-Myc-DriceC211A runs at 30 kDa (lane 3). Lane 1 represents the unprogrammed RRL lysate (no plasmid/transcript added). Lane 2 demonstrates in vitro production of DriceC211A by RRL expression. Lane 3 contains the in vitro cleavage reaction with 6xHis-Droncwt. Lane 4 contains the in vitro cleavage reaction with 6xHis-DroncC318A.
Figure 2C An in vitro cleavage reaction that uses both recombinant and purified caspase (6xHis-Droncwt and 6x-His-DroncC318A) and substrate (6xHis-DriceC211A) according to this protocol, was analyzed by SDS-PAGE and immunoblot. For analysis of the cleavage reaction, the anti-cleaved Drice antibody (diluted 1:5,000; followed by anti-rabbit IgG, HRP-linked antibody (1:10,000)) was used in this immunoblot. The anti-cleaved Drice antibody detects its neo-epitope in the large subunit (23 kDa) of 6xHis-DriceC211A only after processing by 6xHis-Droncwt (lane 1). The catalytic mutant 6xHis-DroncC318A is unable to process 6xHis-DriceC211A in this assay and full-length 6xHis-DriceC211A appears as faint unprocessed band of 35 kDa (lane 2).
<img alt="Figure 1" class="xfigimg" src="/files/ftp_upload/64392/64392fig01.jpg" /> 
Figure 1: Domain structure of initiator caspases Caspase-9 and Dronc and effector caspases Caspase-3 and Drice. CARD - caspase activation and recruitment domain; Cys - relative location of the catalytic Cysteine residue; L - large subunit; S - small subunit. The location of the N-terminal prodomains is indicated. <a href="https://www.jove.com/files/ftp_upload/64392/64392fig01large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 2" class="xfigimg" src="/files/ftp_upload/64392/64392fig02.jpg" /> 
Figure 2: Representative results. (A) Immunoblot analysis of purified recombinant 6xHis-Dronc and 6xHis-Drice preparations, probed with an anti-His antibody. Unprocessed (proDronc and proDrice) and cleaved 6xHis-Dronc and 6xHis-Drice are indicated by arrows. MW markers are indicated on the left. (B) Immunoblot analysis of the in vitro cleavage reaction of RRL-generated N-Myc-Drice with caspases 6xHis-Droncwt (lane 3) or 6x-His-DroncC318A (lane 4) probed with an anti-Myc antibody. Unprogrammed and programmed (N-Myc-DriceC211A) RRL reactions are loaded and separated in lanes 1 and 2. Unprocessed (proDrice) and cleaved N-Myc-Drice are indicated by arrows. MW markers are indicated on the left. (C) Immunoblot analysis of the in vitro cleavage reaction of bacterially expressed and purified recombinant 6xHis-DriceC211A with caspases 6xHis-Droncwt (lane 1) or 6x-His-DroncC318A (lane 2), probed with an anti-cleaved Drice antibody. Full-length (proDrice) and cleaved 6xHis-DriceC211A are indicated by arrows. MW markers are indicated on the left. <a href="https://www.jove.com/files/ftp_upload/64392/64392fig02large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
Supplementary Table 1: This table contains primers used for cloning in pET28a vector. <a href="https://www.jove.com/files/ftp_upload/64392/Supplementary Table1.xlsx" target="_blank">Please click here to download this File.</a>
Supplementary Table 2: This table contains the composition of buffers and media. <a href="https://www.jove.com/files/ftp_upload/64392/Supplementary Table2.xlsx" target="_blank">Please click here to download this File.</a>

Watch this Scientific Journal Video about In Vitro Cleavage Assays using Purified Recombinant Drosophila Caspases for Substrate Screening at JoVE.com

In Vitro Cleavage Assays using Purified Recombinant Drosophila Caspases for Substrate Screening

Here we present a protocol to express and purify recombinant Drosophila caspases Dronc and Drice, and their use in in vitro cleavage assays.

In Vitro Cleavage Assays using Purified Recombinant Drosophila Caspases for Substrate Screening

Caspases are very specific cell death proteases that are involved in apoptotic and non-apoptotic processes. While the role of caspases during apoptosis ...

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1.5K Views.  UMass Chan Medical School. Caspasen zijn cysteïneproteasen die substraten splitsen tijdens apoptose en niet-apoptotische processen. Dit protocol beschrijft een in vitro splitsingstest om vermeende substraten van de initiator caspase Dronc uit Drosophila te identificeren. Indien zorgvuldig gevolgd, biedt dit protocol een betrouwbare procedure voor high throughput screening van vermeende substraten van de caspase Dronc, of een andere caspase.Hoewel dit protocol is ontworpen voor in vitro splitsingstests met behul...

Video: In Vitro Cleavage Assays using Purified Recombinant Drosophila Caspases for Substrate Screening

Lighting Up the Pathways to Caspase Activation Using Bimolecular Fluorescence Complementation

The caspase family of proteases play essential roles in apoptosis and innate immunity. Among these, a subgroup known as initiator caspases are the first to be activated in these pathways. This group includes caspase-2, -8, and -9, as well as the inflammatory caspases, caspase-1, -4, and -5. The initiator caspases are all activated by dimerization following recruitment to specific multiprotein complexes called activation platforms. Caspase Bimolecular Fluorescence Complementation (BiFC) is an imaging-based approach where split fluorescent proteins fused to initiator caspases are used to visualize the recruitment of initiator caspases to their activation platforms and the resulting induced proximity. This fluorescence provides a readout of one of the earliest steps required for initiator caspase activation. Using a number of different microscopy-based approaches, this technique can provide quantitative data on the efficiency of caspase activation on a population level as well as the kinetics of caspase activation and the size and number of caspase activating complexes on a per cell basis.

This protocol describes caspase Bimolecular Fluorescence Complementation (BiFC); an imaging-based method that can be used to visualize induced proximity of initiator caspases, which is the first step in their activation.

The caspase family of proteases play essential roles in apoptosis and innate immunity. Among these, a subgroup known as initiator caspases are the first ...

Biochemistry

Use of Recombinant Fusion Proteins in a Fluorescent Protease Assay Platform and Their In-gel Renaturation

Proteases are intensively studied enzymes due to their essential roles in several biological pathways of living organisms and in pathogenesis; therefore, they are important drug targets. We have developed a magnetic-agarose-bead-based assay platform for the investigation of proteolytic activity, which is based on the use of recombinant fusion protein substrates. In order to demonstrate the use of this assay system, a protocol is presented on the example of human immunodeficiency virus type 1 (HIV-1) protease. The introduced assay platform can be utilized efficiently in the biochemical characterization of proteases, including enzyme activity measurements in mutagenesis, kinetic, inhibition, or specificity studies, and it may be suitable for high-throughput substrate screening or may be adapted to other proteolytic enzymes.
In this assay system, the applied substrates contain N-terminal hexahistidine (His6) and maltose-binding protein (MBP) tags, cleavage sites for tobacco etch virus (TEV) and HIV-1 proteases, and a C-terminal fluorescent protein. The substrates can be efficiently produced in Escherichia coli cells and easily purified using nickel (Ni)-chelate-coated beads. During the assay, the proteolytic cleavage of bead-attached substrates leads to the release of fluorescent cleavage fragments, which can be measured by fluorimetry. Additionally, cleavage reactions can be analyzed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). A protocol for the in-gel renaturation of assay components is also described, as partial renaturation of fluorescent proteins enables their detection based on molecular weight and fluorescence.

Here, we present the detailed procedure of a recently developed protease assay platform utilizing N-terminal hexahistidine/maltose-binding protein and fluorescent protein-fused recombinant substrates attached to the surface of nickel-nitrilotriacetic acid magnetic agarose beads. A subsequent in-gel analysis of the assay samples separated by sodium dodecyl sulfate-polyacrylamide gel electrophoresis is also presented.

Proteases are intensively studied enzymes due to their essential roles in several biological pathways of living organisms and in pathogenesis; therefore, ...

Medium-scale Preparation of Drosophila Embryo Extracts for Proteomic Experiments

Analysis of protein-protein interactions (PPIs) has become an indispensable approach to study biological processes and mechanisms, such as cell signaling, organism development, and disease. It is often desirable to obtain PPI information using in vivo material, to gain the most natural and unbiased view of the interaction networks. The fruit fly Drosophila melanogaster is an excellent platform to study PPIs in vivo, and lends itself to straightforward approaches to isolating material for biochemical experiments. In particular, fruit fly embryos represent a convenient type of tissue to study PPIs, due to the ease of collecting animals at this developmental stage and the fact that the majority of proteins are expressed in embryogenesis, thus providing a relevant environment to reveal most PPIs. Here we present a protocol for collection of Drosophila embryos at medium scale (0.5-1 g), which is an ideal amount for a wide range of proteomic applications, including analysis of PPIs by affinity purification-mass spectrometry (AP-MS). We describe our designs for 1 L and 5 L cages for embryo collections that can be easily and inexpensively set up in any laboratory. We also provide a general protocol for embryo collection and protein extraction to generate lysates that can be directly used in downstream applications such as AP-MS. Our goal is to provide an accessible means for all researchers to carry out the analyses of PPIs in vivo.

Medium-scale Preparation of Drosophila Embryo Extracts for Proteomic Experiments

The goal of this protocol is to provide a straightforward and inexpensive approach to collecting Drosophila embryos at medium scale (0.5-1 g) and preparing protein extracts that can be used in downstream proteomic applications, such as affinity purification-mass spectrometry (AP-MS).

Analysis of protein-protein interactions (PPIs) has become an indispensable approach to study biological processes and mechanisms, such as cell signaling, ...

Developmental Biology

Measuring Caspase Activity Using a Fluorometric Assay or Flow Cytometry

The activation of cysteine proteases, known as caspases, remains an important process in multiple forms of cell death. Caspases are critical initiators and executioners of apoptosis, the most studied form of programmed cell death. Apoptosis occurs during developmental processes and is a necessary event in tissue homeostasis. Pyroptosis is another form of cell death that utilizes caspases and is a critical process in activating the immune system through the activation of the inflammasome, which results in the release of members of the interleukin-1 (IL-1) family. To assess caspase activity, target substrates can be assessed. However, sensitivity can be an issue when examining single cells or low-level activity. We demonstrate how a fluorogenic substrate can be used with a population-based assay or single-cell assay by flow cytometry. With proper controls, different amino acid sequences can be used to identify which caspases are active. Using these assays, the simultaneous loss of the inhibitors of apoptosis proteins upon tumor necrosis factor (TNF) stimulation has been identified, which primarily induces apoptosis in macrophages rather than other forms of cell death.

The present protocol describes two methods to measure caspase activity through a fluorogenic substrate using flow cytometry or a spectrofluorometer.

The activation of cysteine proteases, known as caspases, remains an important process in multiple forms of cell death. Caspases are critical initiators ...

Detecting Anastasis In Vivo by CaspaseTracker Biosensor

Anastasis (Greek for &#8220;rising to life&#8221;) is a recently discovered cell recovery phenomenon whereby dying cells can reverse late-stage cell death processes that are generally assumed to be intrinsically irreversible. Promoting anastasis could in principle rescue or preserve injured cells that are difficult to replace such as cardiomyocytes or neurons, thereby facilitating tissue recovery. Conversely, suppressing anastasis in cancer cells, undergoing apoptosis after anti-cancer therapies, may ensure cancer cell death and reduce the chances of recurrence. However, these studies have been hampered by the lack of tools for tracking the fate of cells that undergo anastasis in live animals. The challenge is to identify the cells that have reversed the cell death process despite their morphologically normal appearance after recovery. To overcome this difficulty, we have developed Drosophila and mammalian CaspaseTracker biosensor systems that can identify and permanently track the anastatic cells in vitro or in vivo. Here, we present in vivo protocols for the generation and use of the CaspaseTracker dual biosensor system to detect and track anastasis in Drosophila melanogaster after transient exposure to cell death stimuli. While conventional biosensors and protocols can label cells actively undergoing apoptotic cell death, the CaspaseTracker biosensor can permanently label cells that have recovered after caspase activation - a hallmark of late-stage apoptosis, and simultaneously identify active apoptotic processes. This biosensor can also track the recovery of the cells that attempted other forms of cell death that directly or indirectly involved caspase activity. Therefore, this protocol enables us to continuously track the fate of these cells and their progeny, facilitating future studies of the biological functions, molecular mechanisms, physiological and pathological consequences, and therapeutic implications of anastasis. We also discuss the appropriate controls to distinguish cells that undergo anastasis from those that display non-apoptotic caspase activity in vivo.

Detecting Anastasis In Vivo by CaspaseTracker Biosensor

Anastasis is technically challenging to detect in vivo because the cells that have reversed the cell death process can be morphologically indistinguishable from normal healthy cells. Here we describe protocols for detecting and tracking cells that undergo anastasis in live animals by using our newly developed in vivo CaspaseTracker biosensor system.

Anastasis (Greek for &#8220;rising to life&#8221;) is a recently discovered cell recovery phenomenon whereby dying cells can reverse late-stage cell death ...

Medicine

Substrate Generation for Endonucleases of CRISPR/Cas Systems

The interaction of viruses and their prokaryotic hosts shaped the evolution of bacterial and archaeal life. Prokaryotes developed several strategies to evade viral attacks that include restriction modification, abortive infection and CRISPR/Cas systems. These adaptive immune systems found in many Bacteria and most Archaea consist of clustered regularly interspaced short palindromic repeat (CRISPR) sequences and a number of CRISPR associated (Cas) genes (Fig. 1) 1-3. Different sets of Cas proteins and repeats define at least three major divergent types of CRISPR/Cas systems 4. The universal proteins Cas1 and Cas2 are proposed to be involved in the uptake of viral DNA that will generate a new spacer element between two repeats at the 5' terminus of an extending CRISPR cluster 5. The entire cluster is transcribed into a precursor-crRNA containing all spacer and repeat sequences and is subsequently processed by an enzyme of the diverse Cas6 family into smaller crRNAs 6-8. These crRNAs consist of the spacer sequence flanked by a 5' terminal (8 nucleotides) and a 3' terminal tag derived from the repeat sequence 9. A repeated infection of the virus can now be blocked as the new crRNA will be directed by a Cas protein complex (Cascade) to the viral DNA and identify it as such via base complementarity10. Finally, for CRISPR/Cas type 1 systems, the nuclease Cas3 will destroy the detected invader DNA 11,12 .
These processes define CRISPR/Cas as an adaptive immune system of prokaryotes and opened a fascinating research field for the study of the involved Cas proteins. The function of many Cas proteins is still elusive and the causes for the apparent diversity of the CRISPR/Cas systems remain to be illuminated. Potential activities of most Cas proteins were predicted via detailed computational analyses. A major fraction of Cas proteins are either shown or proposed to function as endonucleases 4.
Here, we present methods to generate crRNAs and precursor-cRNAs for the study of Cas endoribonucleases. Different endonuclease assays require either short repeat sequences that can directly be synthesized as RNA oligonucleotides or longer crRNA and pre-crRNA sequences that are generated via in vitro T7 RNA polymerase run-off transcription. This methodology allows the incorporation of radioactive nucleotides for the generation of internally labeled endonuclease substrates and the creation of synthetic or mutant crRNAs. Cas6 endonuclease activity is utilized to mature pre-crRNAs into crRNAs with 5'-hydroxyl and a 2',3'-cyclic phosphate termini.

CRISPR/Cas systems mediate adaptive immunity in Bacteria and Archaea. Many Cas proteins are proposed to act as endoribonucleases acting on crRNA precursors of varying length. Here we illustrate three different approaches to generate pre-crRNA substrates for the biochemical analysis of Cas endonuclease activity.

The  interaction of viruses and their prokaryotic hosts shaped the evolution of  bacterial and archaeal life. Prokaryotes developed several strategies to ...

Biology

Identifying Caspases and their Motifs that Cleave Proteins During Influenza A Virus Infection

Caspases, a family of cysteine proteases, orchestrate programmed cell death in response to various stimuli, including microbial infections. Initially described to occur by apoptosis, programmed cell death is now known to encompass three interconnected pathways: pyroptosis, apoptosis, and necroptosis, together coined as one process, PANoptosis. Influence A virus (IAV) infection induces PANoptosis in mammalian cells by inducing the activation of different caspases, which, in turn, cleave various host as well as viral proteins, leading to processes like the activation of the host innate antiviral response or the degradation of antagonistic host proteins. In this regard, caspase 3-mediated cleavage of host cortactin, histone deacetylase 4 (HDAC4), and histone deacetylase 6 (HDAC6) has been discovered in both animal and human epithelial cells in response to the IAV infection. To demonstrate this, inhibitors, RNA interference, and site-directed mutagenesis were employed, and, subsequently, the cleavage or resistance to cleavage and the recovery of cortactin, HDAC4, and HDAC6 polypeptides were measured by western blotting. These methods, in conjunction with RT-qPCR, form a simple yet effective strategy to identify the host as well as viral proteins undergoing caspase-mediated cleavage during an infection of IAV or other human and animal viruses. The present protocol elaborates the representative results of this strategy, and the ways to make it more effective are also discussed.

Influenza A virus (IAV) infection activates the caspases that cleave host and viral proteins, which, in turn, have pro- and antiviral functions. By employing inhibitors, RNA interference, site-directed mutagenesis, and western blotting and RT-qPCR techniques, caspases in infected mammalian cells that cleave host cortactin and histone deacetylases were identified.

Caspases, a family of cysteine proteases, orchestrate programmed cell death in response to various stimuli, including microbial infections. Initially ...

Immunology and Infection

Evaluation of Caspase Activation to Assess Innate Immune Cell Death

Innate immunity provides the critical first line of defense in response to pathogens and sterile insults. A key mechanistic component of this response is the initiation of innate immune programmed cell death (PCD) to eliminate infected or damaged cells and propagate immune responses. However, excess PCD is associated with inflammation and pathology. Therefore, understanding the activation and regulation of PCD is a central aspect of characterizing innate immune responses and identifying new therapeutic targets across the disease spectrum.
This protocol provides methods for characterizing innate immune PCD activation by monitoring caspases, a family of cysteine-dependent proteases that are often associated with diverse PCD pathways, including&#160;apoptosis,&#160;pyroptosis, necroptosis, and PANoptosis. Initial reports characterized caspase-2, caspase-8, caspase-9, and caspase-10 as initiator caspases and caspase-3, caspase-6, and caspase-7 as effector caspases in apoptosis, while later studies found the inflammatory caspases, caspase-1, caspase-4, caspase-5, and caspase-11, drive pyroptosis. It is now known that there is extensive crosstalk between the caspases and other innate immune and&#160;cell death molecules across the previously defined PCD pathways, identifying a key knowledge gap in the mechanistic understanding of innate immunity and PCD and&#160;leading to the characterization of PANoptosis. PANoptosis is a unique innate immune inflammatory PCD pathway regulated by PANoptosome complexes, which integrate components, including caspases,&#160;from other cell death pathways.
Here, methods for assessing the activation of caspases in response to various stimuli are provided. These methods allow for the characterization of PCD pathways both in vitro and in vivo, as activated caspases undergo proteolytic cleavage that can be visualized by western blotting using optimal antibodies and blotting conditions. A protocol and western blotting workflow have been established that allow for the assessment of the activation of multiple caspases from the same cellular population, providing a comprehensive characterization of the PCD processes. This method can be applied across research areas in development, homeostasis, infection, inflammation, and cancer to evaluate PCD pathways throughout cellular processes in health and disease.

This protocol describes a comprehensive method for assessing caspase activation (caspase-1, caspase-3, caspase-7, caspase-8, caspase-9, and caspase-11) in response to both in vitro and in vivo (in mice) models of infection, sterile insults, and cancer to determine the initiation of cell death pathways, such as pyroptosis, apoptosis, necroptosis, and PANoptosis.

Innate immunity provides the critical first line of defense in response to pathogens and sterile insults. A key mechanistic component of this response is ...

In Vivo Biosensor Tracks Non-apoptotic Caspase Activity in Drosophila

Caspases are the key mediators of apoptotic cell death via their proteolytic activity. When caspases are activated in cells to levels detectable by available technologies, apoptosis is generally assumed to occur shortly thereafter. Caspases can cleave many functional and structural components to cause rapid and complete cell destruction within a few minutes. However, accumulating evidence indicates that in normal healthy cells the same caspases have other functions, presumably at lower enzymatic levels. Studies of non-apoptotic caspase activity have been hampered by difficulties with detecting low levels of caspase activity and with tracking ultimate cell fate in vivo. Here, we illustrate the use of an ultrasensitive caspase reporter, CaspaseTracker, which permanently labels cells that have experienced caspase activity in whole animals. This in vivo dual color CaspaseTracker biosensor for Drosophila melanogaster transiently expresses red fluorescent protein (RFP) to indicate recent or on-going caspase activity, and permanently expresses green fluorescent protein (GFP) in cells that have experienced caspase activity at any time in the past yet did not die. Importantly, this caspase-dependent in vivo biosensor readily reveals the presence of non-apoptotic caspase activity in the tissues of organ systems throughout the adult fly. This is demonstrated using whole mount dissections of individual flies to detect biosensor activity in healthy cells throughout the brain, gut, malpighian tubules, cardia, ovary ducts and other tissues. CaspaseTracker detects non-apoptotic caspase activity in long-lived cells, as biosensor activity is detected in adult neurons and in other tissues at least 10 days after caspase activation. This biosensor serves as an important tool to uncover the roles and molecular mechanisms of non-apoptotic caspase activity in live animals.

In Vivo Biosensor Tracks Non-apoptotic Caspase Activity in Drosophila

To detect healthy cells in whole animals that contain low levels of caspase activity, the highly sensitive biosensor designated CaspaseTracker was generated for Drosophila. Caspase-dependent biosensor activity is detected in long-lived healthy cells throughout the internal organs of adult animals reared under optimized conditions in the absence of death stimuli.

Caspases are the key mediators of apoptotic cell death via their proteolytic activity. When caspases are activated in cells to levels detectable by ...

Screening for Genomic Modifications: A Method to Identify CRISPR-Generated Mutants in Drosophila

Source: Du, L., et al. <a href="https://www.jove.com/video/58268/" target="_blank">An Efficient Strategy for Generating Tissue-specific Binary Transcription Systems in Drosophila by Genome Editing</a>. J. Vis. Exp. (2018).
This video describes a screening method to identify transgenic Drosophila flies, whose genome was modified using CRISPR-Cas9. CRISPR-Cas9 is a powerful genome-editing tool that revolutionized the way scientists can manipulate an organism&#39;s genome. In the example protocol, we will see how to identify CRISPR-generated mutants, in which an insertion of a transactivation sequence replaces the first exon of the branchless (bnl) gene, thus creating a bnl gene-specific driver line, bnl-LexA.

Source: Du, L., et al. An Efficient Strategy for Generating Tissue-specific Binary Transcription Systems in Drosophila by Genome Editing. J. Vis. Exp. ...

In Vitro Cleavage Assays using Purified Recombinant Drosophila Caspases for Substrate Screening

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