Name: biotinylated cell-penetrating peptides to study intracellular protein-protein interactions
Uploaded: 2017-12-20T13:00:00.000+00:00
Duration: 10 min 26 s
Description: Watch this Scientific Journal Video about Biotinylated Cell-penetrating Peptides to Study Intracellular Protein-protein Interactions at JoVE.com

We thank M. Morales and J. Bravo for their help with the design of CPPs and J.C. Ar&#233;valo for his help with the pull-down protocol. We are grateful for the technical assistance of T. del Rey. This work was supported by the Ministerio de Econom&#237;a y Competitividad, Spain; FEDER BFU2015-70040-R, Junta de Castilla y Le&#243;n, Spain; FEDER SA026U16 and Fundaci&#243;n Ram&#243;n Areces. M. Jara&#237;z-Rodr&#237;guez and A. Gonz&#225;lez-S&#225;nchez are recipients of a fellowship from the Junta de Castilla y Le&#243;n and the European Social Fund.

All experimental procedures were carried out at the University of Salamanca.
1. Cells
<ol>
	<li>Two days before starting the procedure, plate the cells at the required density to be confluent the day of the experiment. Plate the cells in flasks or plates. However, the protein extraction will be easier from plates. It is convenient to prepare at least 4 plates of 78 cm2 or 2 flasks of 150 cm2 per condition per experiment, to be sure that the results are consistent.</li>
	<li>In this study, plate human G166 GSCs in 4 flasks of 150 cm2, cultured in RHB-A stem cell medium supplemented with 2% B27, 1% N2, 20 ng/mL EGF and b-FGF as described by Pollard et al.22. Process when confluence was reached. For instance, when 5 x 106 G166 cells were plated in a 150 cm2 flask, they were processed 2 days after plating.</li>
</ol>
2. Biotinylated CPPs
<ol>
	<li>Spin the vials containing the lyophilized biotinylated CPPs (BCPPs) at 8200 x g for 30 s, to avoid some of the powder remaining on the lid. Include a control BCPP to be sure that the interactions found are specific of the target sequence. In this study, the control BCPP was TAT-biotin (TAT-B) and the treatment BCPP was TAT-Cx43266-283-B. Other controls could be used, such as TAT fused to scrambled or mutated fragments bond to biotin.</li>
	<li>Dissolve the BCPPs in the corresponding culture medium to the stock solution indicated by the manufacturer; for instance, to obtain a stock solution of 2 mg/mL BCPP to treat GSCs add 0.5 mL of GSC culture medium to one vial containing 1 mg of the BCPP. Vortex and make sure the peptide is well dissolved.</li>
</ol>
3. Tubes
NOTE: Prepare at least twelve 1.5 mL tubes per condition required in the Section 7.
<ol>
	<li>Mark the first 3 tubes per condition. They will have the total volume of cellular lysates obtained in step 6.4.</li>
	<li>Mark an A in 3 tubes per condition. These tubes will have the first supernatants obtained after lysing and spinning the cellular lysates, step 7.2.</li>
	<li>Mark a B in 3 tubes per condition. These tubes will have a small aliquot of the first supernatants. These lysates will serve as the Western blot samples in step 7.3.</li>
	<li>Mark a C in 3 tubes per condition. These tubes will have the supernatants obtained after the pull-down with NeutrAvidin, step 7.7. 
	NOTE: This is important in case the Western blot showed no signal for proteins, meaning the proteins were not pulled down or were lost at some step of the procedure. If this were the situation, repeat the process to pull down the proteins.</li>
</ol>
4. Cellular treatment with the BCPPs
<ol>
	<li>Aspirate the culture medium.</li>
	<li>Replace the corresponding volume of fresh medium required to incubate the BCPPs in the smallest possible volume of medium according to the incubation times. It is very important that in any case, the medium covers completely the whole surface of the plate/flask so that the cells do not dry out, for instance, 6 mL per 150 cm2 for a 30 min incubation.</li>
	<li>Add the volume of the stock solution of BCPP to the cell cultures to reach the concentration that has been proved to be effective. In this study 50 &#181;M TAT-Cx43266-283-B has been proved to reduce GSC proliferation.
	<ol>
		<li>Therefore, add 92.8 &#181;L of 2 mg/mL TAT-Cx43266-283-B (MW=3723.34 g/mol) per mL of culture medium to obtain a final concentration of 50 &#181;M TAT-Cx43266-283-B. If the volume to be added is different for control peptides, complete with culture medium up to the same final volume. For instance, 49.1 &#181;L TAT-B (MW=1914.31 g/mol) plus 43.7 &#181;L GSC medium were added per mL of culture medium to obtain a final concentration of 50 &#181;M TAT-B.</li>
	</ol>
	</li>
	<li>Place the cells in the incubator at 37 &#176;C and 5% CO2 for 30 min to make sure that the interactions between the BCPP and its intracellular partners take place. If the interaction takes longer, incubate for longer times or adjust times in case the experiment consisted of a time-course. In addition, the interaction of interest can be promoted or prevented by stimulating different intracellular signaling pathways.</li>
</ol>
5. Buffers and solutions.
<ol>
	<li>Prepare PBS pH 7.4: 136 mM NaCl; 2.7 mM KCl; 7.8 mM Na2HPO4&#183;2H2O; 1.7 mM KH2PO4.</li>
	<li>Prepare protein lysis buffer: 20 mM Tris-HCl (pH 8.0), 137 mM NaCl, 1% IGEPAL, Prior to use, add the following: 1/100 (v/v) Protease Inhibitor Cocktail, 1 mM Sodium Fluoride, 1 mM Phenylmethanesulfonyl fluoride (PMSF) and 0.1 mM Sodium orthovanadate.</li>
	<li>Prepare Laemmli buffer: (4x: 0.18 M Tris-HCl pH 6.8; 5 M glycerol; 3.7 % SDS (p/v); 0.6 M &#946;-mercaptoethanol or 9 mM DTT; 0.04 % (v/v) bromophenol blue (BB)).</li>
</ol>
6. Protein extraction
NOTE: Protein extraction was performed as previously described20,23. Carry out this whole section of the procedure at 4 &#176;C.
<ol>
	<li>Aspirate the culture medium completely.</li>
	<li>Wash 3 x 10 mL of with ice-cold phosphate buffered saline (PBS) per 150 cm2 very carefully to avoid cell detachment.</li>
	<li>To obtain the cell lysate, add 3 mL of lysis buffer per 150 cm2 and thoroughly scrape the surface by using a cell scraper. Tilting the plate/flask to about 45 degrees will make easier to gather the cell lysates into their corresponding tubes.</li>
	<li>Pour 1 mL of the cellular lysate per tube in three 1.5 mL tubes. These tubes will be marked with the condition and the replicate as indicated in step 3.1.</li>
</ol>
7. Pull-down
<ol>
	<li>Centrifuge the 1.5 mL tubes at 11,000 x g for 10 min at 4 &#176;C.</li>
	<li>Transfer the supernatants to new tubes (A).</li>
	<li>Take an aliquot of this supernatant per condition to different tubes (B), i.e. 50 &#181;L per tube. Add 4x Laemmli buffer (16.6 &#181;L for 50 &#181;L of lysate) and freeze at -20 &#176;C. These lysates will serve as usual Western blot samples.</li>
	<li>Homogenize very well the NeutrAvidin Agarose by gentle shaking. Cut the tips of the pipette tips to increase their diameter and improve the pipetting of the beads. Add 50 &#181;L of NeutrAvidin Agarose per mL of cell lysate in the (A) tubes.</li>
	<li>Incubate at 4 &#176;C overnight with very gentle shaking to allow NeutrAvidin to interact with BCPPs bound to their intracellular partners.</li>
	<li>Centrifuge at 3,000 x g for 1 min at 4 &#176;C to collect the complex of NeutrAvidin with proteins.</li>
	<li>Carefully remove the supernatants and transfer them to clean tubes (C). Keep them to use them in case the pull-down is not successful.</li>
	<li>Washing steps: add fresh lysis buffer to the pellets (tubes A), resuspend by inversion and repeat the steps 7.6) and 7.7) for 5 more times. All these supernatants can be discarded.</li>
	<li>Remove the supernatants and add 2x Laemmli buffer to the desired final volume (40 &#181;L per 1.5 mL tube for pellets obtained from 150 cm2 flasks of confluent cells).</li>
	<li>Elute at 100 &#176;C for 5 min to dissociate the interactions between proteins and centrifuge for 30 s at 8,200 x g to pellet NeutrAvidin beads.</li>
	<li>Take the supernatants, containing the dissociated proteins, with capillary tips to new tubes (D). The beads can be kept in case repeating elution steps is required. 
	NOTE: The supernatants (tubes D) are now ready to be loaded in Western blot or to freeze at -20 &#176;C.</li>
</ol>
8. Western Blot
NOTE: Western blotting was performed as previously described24.
<ol>
	<li>Load equivalent volume of each sample per lane on Bis-Tris (4-12%) midigels in a Midi-Cell Electrophoresis System.</li>
	<li>Transblot proteins using a dry blotting system into a nitrocellulose regular stack.</li>
	<li>Stain the membrane with 10% Ponceau for 10 min.</li>
	<li>Wash the membranes 3 x 5 min with 5 mL of TTBS.</li>
	<li>Block the membranes with 7% milk in TTBS for 1 h with gentle shaking in tubes or small boxes. Make sure the volume used is enough to cover the membranes and that they do not dry, i.e. 40 mL per whole midi membrane.</li>
	<li>Wash 3 x 5 min with 5 mL of TTBS.</li>
	<li>Incubate overnight at 4 &#176;C with the primary antibody against the protein of interest with gentle shaking.</li>
	<li>Wash 3 x 5 min with 5 mL of TTBS.</li>
	<li>Incubate the membrane at room temperature with the correspondent peroxidase-conjugated secondary antibody in TTBS for 1 h.</li>
	<li>Wash 3 x 5 min with 5 mL of TTBS.</li>
	<li>Develop with a chemiluminescent substrate in a chemiluminescence system.</li>
</ol>
9. Problem Solving
<ol>
	<li>If after developing the Western blot any of the samples showed no signal at all for proteins, check the Ponceau. 
	NOTE: The membrane in Ponceau should show undefined and numerous bands along the lanes loaded. If the bands are not very noticeable, the quantity of proteins loaded may not be enough or the transference may have gone incorrectly. Consider repeating the Western blot.</li>
	<li>If there is no stain at all in the Ponceau membrane in any lane, repeat the whole procedure from the step 7.4 in the (C) tubes.</li>
	<li>If after developing the Western blot a protein signal is very weak but the Ponceau showed proteins, incubate again the membrane with the primary antibody for longer time. If the signal is still rather weak, incubate again at room temperature.</li>
</ol>
10. Other Techniques Used in this Article
<ol>
	<li>Immunocytochemistry of BCPPs
	<ol>
		<li>Fix cells in 4% paraformaldehyde (0.2 mL per cm2) for 20 min.</li>
		<li>Wash 3x 5 min with PBS (0.2 mL per cm2).</li>
		<li>Apply the corresponding antibody (at least 0.15 mL per cm2) diluted in antibody solution at the manufacturer&#39;s indicated concentration against your protein of interest overnight at 4 &#176;C.</li>
		<li>Incubate with a fluorophore-conjugated secondary antibody (0.15 mL per cm2) for 2 h at room temperature.</li>
		<li>Repeat steps 10.1.2-10.1.4 with other antibodies against your proteins of interest. Be careful not to use the same species for different primary antibodies or same wavelength fluorophores for secondary antibodies.</li>
		<li>Mount the cells using the antifade reagent (0.005 mL per cm2).</li>
		<li>Analyze on a fluorescence microscope connected to a digital camera.</li>
	</ol>
	</li>
	<li>MTT assay
	<ol>
		<li>Culture the cells at 37 &#176;C in 24-well plates.</li>
		<li>Incubate the cells in the dark for 75 min with 0.15 mL of culture medium per cm2 containing 0.5 mg/mL MTT.</li>
		<li>Aspirate the medium and incubate the cells for 10 min in the dark with dimethyl sulfoxide (0.25 mL per cm2) with mild shaking.</li>
		<li>Measure the absorbance at a wavelength of 570 nm using a microplate reader.</li>
	</ol>
	</li>
</ol>

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The authors have nothing to disclose.

There are many methods to study protein-protein interactions. The method presented in this study is based on the widely used biotin-avidin pull-down system in which a biotinylated bait is incubated with cell lysates to allow the establishment of interactions. The modification presented in this study includes the combination of this technique with cell-penetrating sequences. We propose to design cell-penetrating baits that can be incubated with living cells instead of cell lysates and therefore the interactions found will reflect those that occurred within the cellular context.
Here we use TAT as the cell-penetrating sequence, biotin as the pull-down tag and the region of Cx43 comprised between amino acids 266-283 as the target to find intracellular interactions in human GSCs. The structural basis for the interaction between Cx43 and c-Src is well known11,12. This is an important interaction because it inhibits the oncogenic activity of c-Src in glioma cells24,13. In fact, CPPs containing this region (TAT-Cx43266-283) mimic the antioncogenic properties of Cx43 on glioma cells19,20,21. In rat glioma C6 cells, the mechanism by which TAT-Cx43266-283 inhibits c-Src includes the recruitment of c-Src together with its endogenous inhibitors CSK and PTEN20. It should be mentioned that GSCs are very interesting as a target in glioma therapy, because they constitute a subpopulation that is resistant to conventional treatments and therefore responsible for the recurrence of this malignant brain tumors27. Furthermore, they are hard-to-transfect cells and therefore the study of intracellular interactions becomes more difficult. CPPs are rapidly and efficiently internalized in GSCs19 favoring their use for the study of intracellular interactions. In this study, using CPPs fused to biotin we confirm the interaction of the Cx43266-283 sequence with c-Src together with its endogenous inhibitors CSK and PTEN in human GSCs.
This method is very powerful to study the intracellular mechanism of bioactive compounds. However, it is very important to confirm that the biological effect of the biotinylated cell penetrating bait is not different from that obtained with the non-biotinylated one. This step is required to associate the interactions found with the effect of the bioactive compound. In addition, the stability of the compound, its possible degradation by proteases as well as its possible toxicity, should be carefully tested and taken into account before planning the experiment. In the example presented, the anti-proliferative effect of TAT-Cx43266-283 on G166 human GSCs has been previously documented20. In this study, we confirm that the anti-proliferative effect of TAT-Cx43266-283-B and of TAT-Cx43266-283 is very similar. In addition, the analysis of cellular morphology revealed that &#945;-tubulin and F-actin distribution is very similar in G166 GSCs treated with TAT-Cx43266-283-B or with TAT-Cx43266-283. Altogether, these results indicate that the inclusion of biotin at the c-terminus of TAT-Cx43266-283 did not modify the effects of this compound on human GSCs. However, if biotin would modify the effects of the bioactive molecule, other tags for protein purification can be tested, such as the FLAG octapeptide (DYKDDDDK)28, the human influenza hemagglutinin-derived tag HA (YPYDVPDYA) or glutathione S-transferase (GST)29. Similarly, if TAT does not target the cell population of interest, other cell penetrating sequences, such as penetratin, MPG (for a review, see30) or cell specific sequences can be used31.
In addition to study proteins that specifically interact with the target sequence, ideally, the presence of proteins that interact with both the control and the target sequence and proteins that do not interact with them, as positive and negative controls, should be addressed. In this sense, we found Cav-1 in the control and treated situation, suggesting that the caveolae have been involved in the mechanism of internalization, as it has been previously shown26. Furthermore, FAK, which interacts with c-Src but is supposed not to interact with the Cx43 c-terminal, was absent in both the control and treated situation. These results reinforce the specificity of the interaction between TAT-Cx43266-283-B, c-Src, CSK and PTEN.To confirm the results obtained with this protocol, confocal microscopy can be used to visualize the distribution of the interacting proteins and to study their co-localization. Thus, we found that TAT-Cx43266-283-B and c-Src exhibit a similar intracellular distribution with some points of co-localization confirming the results obtained with the pull-down experiments. In fact, TAT-Cx43266-283-B is distributed close to the plasma membrane suggesting that the cargo, in this study Cx43266-283, directs the molecule to its intracellular partners.
One of the limitations of the proposed method is that the molecule used as bait could fail to fold properly and the expected effects would not be found. In this situation, the interactions found could not be associated to the effect. However, this method can be especially interesting for the interactions involved in signal transduction pathways because they are usually carried out by intrinsically disordered regions32 and therefore they do not require an ordered folding. In addition, one of the advantages of the proposed method is that the time course of the interaction can be followed, which is especially relevant for transient interactions. Furthermore, the relevance of each residue on the interaction can be easily studied. Indeed, it is possible to study the relevance of posttranslational modifications on protein-protein interaction, for instance, by phosphomimetic substitution of glutamate for serine or threonine. Similarly, substitution of serine or threonine for alanine or tyrosine for phenylalanine allows testing the effect of non-phosphorylatable serine, threonine or tyrosine. To mimic phospho-tyrosine, the most accurate way is the substitution of Tyr for p-Tyr33.
Finally, the scope of this protocol is far beyond protein-protein interaction because this system can be applied to other bioactive cargoes such as RNA sequences, nanoparticles, viruses or other molecules that can be fused to biotin and transduced with CPP to study their intracellular mechanism of action.

Protein-protein interactions are essential for a great variety of cellular processes. To fully understand these processes, methods for identifying protein interactions within the complex intracellular environment are required. One of the most used methods to identify interaction partners of a protein is to use that protein or a mimetic peptide of a part of that protein as bait in affinity pull-down experiments followed by detection of binding proteins. The avidin-biotin system is frequently used because of the high affinity, specificity and stable interaction between avidin and biotin1,2. Usually, biotin is covalently bound to the bait (protein or peptide) and after a period of incubation with the cell lysates to allow the establishment of interactions, the biotinylated bait bound to its intracellular partners is pulled down with avidin or avidin derivatives conjugated with support beads. Then, bait-protein interactions are detected after washing, elution, and analysis by denaturing electrophoresis followed by Western blot. One of the problems of this technique is that the interactions between the protein of interest and its intracellular partners are taking place outside of the cellular context. This is especially important for the interactions involved in signal transduction pathways because they take place in specific intracellular locations, they are transient and they are typically carried out by not abundant proteins. Therefore, within the cell lysates these interactions can be masked by other more abundant proteins or by proteins that usually are not in close proximity.
Cell-penetrating peptides (CPPs) are short peptides (&#8804;40 amino acids), composed mostly by cationic amino acids that are capable of transporting a wide range of molecules into almost any cell3. Cargoes such as proteins, plasmid DNA, siRNA, viruses, imaging agents, and various nanoparticles have been conjugated to CPPs and efficiently internalized4,5. Because of this transporting ability they are also known as protein transduction domains (PTDs), membrane translocating sequences (MTSs), and Trojan peptides. Among the CPPs, the TAT peptide from the HIV transactivator protein TAT6 has been one of the most widely studied 7,8,9. TAT is a nonapeptide that contains 6 arginine and 2 lysine residues and consequently is highly cationic. Substitution studies have demonstrated that the net positive charge of TAT is necessary for electrostatic interactions with the plasma membranes of eukaryotic cells and its subsequent internalization10. Similarly to other CPPs, positively-charged TAT strongly binds electrostatically to the various negatively-charged species present at the extracellular surface of cell membranes, including lipid head groups, glycoproteins and proteoglycans3,10. The bioactive cargoes transported by TAT become immediately free in the cytosol to reach their intracellular partners.
Here we present a method that combines the TAT CPP with biotin to study intracellular interactions. The aim is to design cell-penetrating baits by fusing the target biomolecule to TAT and to biotin. The main advantage of this proposal is that the interactions between the bait and its partners will take place within its cellular context. To show the efficacy of this method we used as bait a small sequence of the protein Cx43 that has been reported to interact intracellularly with the proto-oncogene c-Src11,12,13. Cx43 is an integral membrane protein that is widely expressed in astrocytes14and is down-regulated in high-grade gliomas, the most common malignant tumor of the central nervous system15,16,17,18.It has been previously shown that the Cx43 region that interacts with c-Src (amino acids 266-283 in human Cx43; Pubmed: P17302) fused to TAT (TAT-Cx43266-283) inhibits the oncogenic activity of c-Srcin glioma cells and glioma stem cells (GSCs)19,20,21. To design the intracellular bait, Cx43266-283 has been fused to TAT at the N-terminus (TAT-Cx43266-283) and to biotin at the C-terminus (TAT-Cx43266-283-B). This strategy has been successfully used in the rat glioma C6 cell line to identify c-Src, c-terminal Src kinase (CSK) and phosphatase and tensin homolog (PTEN) as intracellular partners of this region of Cx4320. Here, we describe this method testing its efficacy in human GSCs, which are very relevant for glioma therapy but much harder to transfect than non-stem glioma cells.

<table><tbody><tr><td>G166 GSC line</td><td>BioRep</td><td></td><td></td></tr><tr><td>RHB-A stem cell medium</td><td>Takara</td><td>Y40001</td><td></td></tr><tr><td>Laminin Mouse Protein</td><td>Invitrogen, Life Technologies, ThermoFisher Scientific</td><td>23017-015</td><td>10 &amp;micro;g/ml</td></tr><tr><td>B-27 Serum free Supplement (50X)</td><td>Invitrogen, Life Technologies, ThermoFisher Scientific</td><td>17504-044</td><td>2%</td></tr><tr><td>N-2 Supplement (100x)</td><td>Invitrogen, Life Technologies, ThermoFisher Scientific</td><td>17502-048</td><td>1%</td></tr><tr><td>Recombinant Human EGF</td><td>Peprotech</td><td>AF-100-15</td><td>20 ng/ml</td></tr><tr><td>Recombinant Human b-FGF</td><td>Peprotech</td><td>AF-100-18B</td><td>20 ng/ml</td></tr><tr><td>PBS pH 7.4: In deionized water, 136 mM NaCl ; 2.7 mM KCl; 7.8 mM Na2HPO4&amp;middot;2H2O ; 1.7 mM KH2PO4</td><td></td><td></td><td></td></tr><tr><td>Accutase</td><td>Sigma</td><td>A6964</td><td></td></tr><tr><td>Cryostor CS10 cryopreservation medium</td><td>StemCell Technologies</td><td>7930</td><td></td></tr><tr><td>TAT</td><td>GenScript</td><td>-</td><td>Custom made</td></tr><tr><td>TAT-B</td><td>GenScript</td><td>-</td><td>Custom made</td></tr><tr><td>TAT-Cx43&lt;sub&gt;266-283&lt;/sub&gt;</td><td>GenScript</td><td>-</td><td>Custom made</td></tr><tr><td>TAT-Cx43&lt;sub&gt;266-283&lt;/sub&gt;-B</td><td>GenScript</td><td>-</td><td>Custom made</td></tr><tr><td>Alexa Fluor 594 Phalloidin</td><td>Molecular Probes, Life Technologies, ThermoFisher Scientific</td><td>A1275737</td><td>1/20</td></tr><tr><td>Monoclonal &amp;alpha;-tubulin mouse antibody</td><td>Sigma-Aldrich</td><td>T9026</td><td>1/500</td></tr><tr><td>4&#039;,6-diamidino-2-phenylindole (DAPI)</td><td>Molecular Probes, Life Technologies, ThermoFisher Scientific</td><td></td><td>1.25 mg/ml</td></tr><tr><td>Pierce&amp;trade; NeutrAvidin&amp;trade; Agarose</td><td>ThermoFisher Scientific</td><td>29200</td><td></td></tr><tr><td>Protein lysis buffer: 5 mM Tris-HCl (pH 6.8), 2% (w/v) SDS, 2 mM EDTA , 2 mM EGTA</td><td></td><td></td><td></td></tr><tr><td>Protease Inhibitor Cocktail Set III. EDTA-Free</td><td>Calbiochem, Bionova</td><td>539134</td><td>1/100 (v/v)</td></tr><tr><td>Sodium Fluoride</td><td>PanReac AppliChem</td><td>141675</td><td>1 mM</td></tr><tr><td>Phenylmethanesulfonyl fluoride (PMSF)</td><td>Sigma-Aldrich</td><td>P7626</td><td>1 mM</td></tr><tr><td>Sodium orthovanadate</td><td>Sigma-Aldrich</td><td>S6508</td><td>0.1 mM</td></tr><tr><td>Laemmli buffer: (4x: 0.18 M Tris-HCl pH 6.8; 5 M glycerol; 3.7 % (w/v) SDS; 0.6 M &amp;beta;-mercaptoethanol or 9 mM DTT ; 0.04% (v/v) bromophenol blue (BB) .</td><td></td><td></td><td>1X</td></tr><tr><td>Xcell 4 SureLock Midi-Cell Electrophoresis System</td><td>Life Technologies, ThermoFisher Scientific</td><td>WR0100</td><td></td></tr><tr><td>NuPAGE Novex Bis-Tris Midi-Gels 4-12%</td><td>Life Technologies, ThermoFisher Scientific</td><td>WG1402box</td><td></td></tr><tr><td>NuPAGE MOPS SDS Running Buffer (20X)</td><td>Life Technologies, ThermoFisher Scientific</td><td>NP0001</td><td>1X</td></tr><tr><td>NuPAGE Transfer Buffer 20x</td><td>Life Technologies, ThermoFisher Scientific</td><td>NP0006</td><td>1X</td></tr><tr><td>Precision Plus Protein Dual Color Standard</td><td>Bio-Rad</td><td>161-0374</td><td></td></tr><tr><td>iBlot 2 NC Regular Stacks (nitrocellulose membranes)</td><td>Life Technologies, ThermoFisher Scientific</td><td>IB23001</td><td></td></tr><tr><td>iBlot 2 Dry Blotting System - Gel transfer device</td><td>Life Technologies, ThermoFisher Scientific</td><td>IB21001</td><td></td></tr><tr><td>10% Ponceau S Solution (0.1% Ponceau (w/v) in 5% acetic acid (v/v)) in water</td><td>Sigma</td><td>P7170</td><td></td></tr><tr><td>FAK polyclonal rabbit antibody</td><td>Life Technologies, ThermoFisher Scientific</td><td>AHO0502</td><td>1/500</td></tr><tr><td>Src polyclonal rabbit antibody</td><td>Cell Signalling (WERFEN)</td><td>2108S</td><td>1/500</td></tr><tr><td>Csk polyclonal rabbit antibody</td><td>Cell Signalling (WERFEN)</td><td>4980</td><td>1/500</td></tr><tr><td>PTEN polyclonal mouse antibody</td><td>Cell Signalling (WERFEN)</td><td>9552</td><td>1/500</td></tr><tr><td>Caveolin-1 polyclonal rabbit antibody</td><td>Abcam</td><td>ab2910</td><td>1/1000</td></tr><tr><td>Goat anti-mouse IgG-HRP antibody</td><td>Quimigen, Santa Cruz Biotechnology</td><td>Sc-2005</td><td>1/5000</td></tr><tr><td>Goat anti-rabbit IgG-HRP antibody</td><td>Quimigen, Santa Cruz Biotechnology</td><td>SC-2030</td><td>1/5000</td></tr><tr><td>Western Blotting Luminol Reagent</td><td>Santa Cruz Biotechnology</td><td>SC-2048</td><td></td></tr><tr><td>Src polyclonal rabbit antibody</td><td>Cell Signalling (WERFEN)</td><td>2108S</td><td>1/500</td></tr><tr><td>Antibody solution: PBS, 10% FBS, 0.1 M lysine, 0.02% sodium azide</td><td></td><td></td><td></td></tr><tr><td>Alexa Fluor 488 goat anti-mouse IgG</td><td>Invitrogen, Life Technologies, ThermoFisher Scientific</td><td>A11029</td><td>1/1000</td></tr><tr><td>Cy2-conjugated streptavidin</td><td>Jackson ImmunoResearch</td><td>016-220-089</td><td>1/500</td></tr><tr><td>MicroChemi Luminescence system</td><td>DNA Bio-Imaging Systems</td><td></td><td></td></tr><tr><td>Dead Cell Apoptosis Kit with Annexin V Alexa Fluor&amp;reg; 488 &amp;amp; Propidium Iodide (PI)</td><td>Molecular Probes, Life Technologies, ThermoFisher Scientific</td><td>V13241</td><td>1/500</td></tr><tr><td>SlowFade Gold antifade reagent</td><td>Life Technologies, ThermoFisher Scientific</td><td>S36936</td><td></td></tr><tr><td>Thiazolyl Blue Tetrazolium Bromide (MTT)</td><td>Sigma-Aldrich</td><td>M2128</td><td></td></tr><tr><td>Dimethyl sulfoxide for UV-spectroscopy, &gt;=99.8% (GC)</td><td>Honeywell</td><td>41641-1L</td><td></td></tr><tr><td>Appliskan 2001</td><td>Thermo Electron Corporation, Thermo Scientific</td><td></td><td></td></tr></tbody></table>

biotinylated cell-penetrating peptides to study intracellular protein-protein interactions

Here we present a protocol to study intracellular protein-protein interactions that is based on the widely used biotin-avidin pull-down system. The modification presented includes the combination of this technique with cell-penetrating sequences. We propose to design cell-penetrating baits that can be incubated with living cells instead of cell lysates and therefore the interactions found will reflect those that occur within the intracellular context. Connexin43 (Cx43), a protein that forms gap junction channels and hemichannels is down-regulated in high-grade gliomas. The Cx43 region comprising amino acids 266-283 is responsible for the inhibition of the oncogenic activity of c-Src in glioma cells. Here we use TAT as the cell-penetrating sequence, biotin as the pull-down tag and the region of Cx43 comprised between amino acids 266-283 as the target to find intracellular interactions in the hard-to-transfect human glioma stem cells. One of the limitations of the proposed method is that the molecule used as bait could fail to fold properly and, consequently, the interactions found could not be associated with the effect. However, this method can be especially interesting for the interactions involved in signal transduction pathways because they are usually carried out by intrinsically disordered regions and, therefore, they do not require an ordered folding. In addition, one of the advantages of the proposed method is that the relevance of each residue on the interaction can be easily studied. This is a modular system; therefore, other cell-penetrating sequences, other tags, and other intracellular targets can be employed. Finally, the scope of this protocol is far beyond protein-protein interaction because this system can be applied to other bioactive cargoes such as RNA sequences, nanoparticles, viruses or any molecule that can be transduced with cell-penetrating sequences and fused to pull-down tags to study their intracellular mechanism of action.

Before using BCPPs to study intracellular interaction, it is critical to compare the effects of BCPP vs CPP to validate the results obtained with BCPP. Consequently, to study whether the inclusion of biotin modifies the activity of the target sequence, we first analyzed the effect of TAT-Cx43266-283-B compared with TAT-Cx43266-283 on G166 GSCs morphology. To do so, we performed some immunofluorescence analyses of two cytoskeletal proteins, F-actin and &#945;-tubulin after 24 h of treatment. Figure 1 shows that G166 GSCs in the presence of 50 &#181;M TAT-Cx43266-283 or TAT-Cx43266-283-B acquire a more rounded shape compared to the elongated and expanded cellular prolongations shown in the controls (TAT or TAT-B). In fact, Figure 1b shows that actin filaments are mostly assembled as actin networks when the cells were treated with TAT-Cx43266-283 or TAT-Cx43266-283-B while they form more actin bundles in the control cells (treated with TAT or TAT-B)25. In contrast, &#945;-tubulin distribution does not vary between the different conditions. These results showed that the presence of biotin did not modify the effect of the target sequence on the morphology of G166 GSCs. In previous studies20,21, we showed that TAT-Cx43266-283 reduced G166 GSCs proliferation. In this study, we investigated whether TAT-Cx43266-283-B exerts the same effects in the growth as TAT-Cx43266-283. To do so, we analyzed the G166 GSCs proliferation by MTT assay after 72 h of treatment. The MTT assay is a colorimetric assay for assessing cell metabolic activity. MTT is metabolized by NAD(P)H oxidoreductase enzymes in mitochondria reflecting the number of viable cells present. Figure 2 shows that the reduction in the G166 GSCs cell viability is not significantly different when cells were treated with 50 &#181;M TAT-Cx43266-283 or 50 &#181;M TAT-Cx43266-283-B. Indeed, both significantly diminished G166 GSCs proliferation as compared to the control, TAT or TAT-B.
Once we confirmed that the effect of our target sequence in G166 GSCs (TAT-Cx43266-283) was not modified by the inclusion of biotin at the C-terminus (TAT-Cx43266-283-B), we investigated the intracellular partners of this sequence following the protocol described in this study (Figure 3). Because caveolae have been involved in the mechanism of TAT internalization26, we analyzed the presence of caveolin-1 (Cav-1) in the pull-downs. Western blot analysis (Figure 4) showed that TAT-B and TAT-Cx43266-283-B interact with Cav-1. However, the ability of TAT-Cx43266-283-B to recruit c-Src, PTEN and CSK is stronger than that found with TAT-B. Focal adhesion kinase (FAK) is a substrate of c-Src that has not been shown to interact with Cx43. Indeed, FAK did not show any significant interaction with either TAT-B or TAT-Cx43266-283-B.
To confirm the interaction between TAT-Cx43266-283-B and c-Src, G166 GSCs were incubated with 50 &#181;M TAT-Cx43266-283-B for 30 min and their localization was followed with fluorescent streptavidin by confocal microscopy (Figure 5). Our results showed that the intracellular distribution of TAT-Cx43266-283-B is close to the plasma membrane (shown by phosphatidylserine staining) and matches with that of c-Src. In fact, co-localization analyses revealed some points of co-localization (white) between TAT-Cx43266-283-B and c-Src in the merge image. Consequently, confocal microscopy studies confirm the results obtained with the BCPP pull-down protocol described in this study.

<img alt="Figure 1" class="xfigimg" src="/files/ftp_upload/56457/56457fig1.jpg" /> 
Figure 1: Effect of BCPP and CPP on GSC morphology. 
G166 GSCs were plated at a low density (2 x 104 cells / cm2) and after 24 h they were incubated with 50 &#181;M control CPP (TAT), control BCPP (TAT-B), treatment CPP (TAT-Cx43266-283) or treatment BCPP (TAT-Cx43266-283-B). a) F-actin (red), &#945;-tubulin (green) and merged + DAPI immunostaining of the same field showing G166 GSCs morphology. Bars = 50 &#181;m. b) F-actin immunostaining showing the different distribution of F-actin in G166 GSCs after incubation for 24 h with 50 &#181;M control CPP (TAT) or control BCPP (TAT-B) as compared with 50 &#181;M treatment CPP (TAT-Cx43266-283) or BCPP (TAT-Cx43266-283-B). Bars = 10 &#181;m. <a href="https://cloudflare.jove.com/files/ftp_upload/56457/56457fig1large.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/56457/56457fig2.jpg" /> 
Figure 2: Effect of BCPP and CPP on GSC viability. 
G166 GSCs were plated at 5500 cells/cm2 in 24-multiwell plates and incubated with 50 &#181;M control peptides, CPP (TAT) or BCPP (TAT-B), or 50 &#181;M treatment peptides, CPP (TAT-Cx43266-283) or BCPP (TAT-Cx43266-283-B). The cell viability was analyzed using a MTT assay after 72 h. The results are expressed as MTT absorbances and are the mean &#177; s.e.m. of at least 3 experiments (++ p&#706;0.01 vs control. ** p&#706;0.01, *** p&#706;0.001 vs TAT or TAT-B; one-way ANOVA withTukey post-test). Note that there are not significant differences between the effects of CPPs vs BCPPs. <a href="https://cloudflare.jove.com/files/ftp_upload/56457/56457fig2large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 3" class="xfigimg" src="/files/ftp_upload/56457/56457fig3.jpg" /> 
Figure 3: Protocol diagram. 
Step by step graphical depiction of the procedure as described in the section &#34;Protocol&#34;, from the incubation of the BCPPs until the eluted BCPPs and their interacting proteins were obtained.1) Incubate culture cells with BCPPs at the desired concentration for the required time. 2) During the incubation, the BCPPs are internalized and they interact with their intracellular partners. 3) Wash the cells three times on ice with ice-cold PBS. 4) Lyse the cells to extract proteins. 5) Transfer cell lysates to tubes. 6) Spin at 11000 x g for 10 min at 4 &#176;C. 7) Transfer the supernatants to new tubes (A) and keep a small aliquot of the lysates to process as regular Western blot samples in tube (B). 8) Resuspend the NeutrAvidin Agarose beads and add 50 &#181;L to each tube A using a cut pipette tip. 9) Incubate with gently shaking for 12 h at 4 &#176;C to allow the NeutrAvidin agarose beads to interact with BCPPs and their partners. 10) Spin for 1 min at 3000 x g to pellet the beads with the biotinylated baits and their interacting proteins bound to them. 11) Transfer supernatants to new tubes (C) and keep them to use in case the pull-down need to be repeated. 12) Wash the pellet five times with fresh lysis buffer, resuspend by inversion, spin for 1 min at 3000 x g and discard the supernatant. 13) Remove all the supernatant carefully. 14) Add the desired volume of 4x Laemmli buffer and elute the proteins at 100 &#176;C for 5 min. 15) Spin at 8200 x g for 30 s to pellet the beads. 16) Transfer the eluted proteins found in the supernatant with capillary tips to new tubes (D). 17) Load onto gels for Western blot analysis. <a href="https://cloudflare.jove.com/files/ftp_upload/56457/56457fig3large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 4" class="xfigimg" src="/files/ftp_upload/56457/56457fig4.jpg" /> 
Figure 4: Study of the intracellular interactions of TAT-Cx43266-283-B in G166 GSCs by pull-down followed by Western blot. 
G166 GSCs were incubated with 50 &#181;M TAT-B or TAT-Cx43266-283-B. After 30 min the cells were lysed and TAT-B or TAT-Cx43266-283-B attached to their intracellular partners were pulled down with NeutrAvidin beads. The eluted proteins were loaded and analyzed by Western blot to study the levels of FAK, c-Src, CSK, PTEN and Cav-1. Note that Cav-1 interacts with both TAT-B and TAT-Cx43266-283-B, c-Src, PTEN and CSK interact preferentially with TAT-Cx43266-283-B and FAK did not show any interaction with either TAT-B or TAT-Cx43266-283-B. <a href="https://cloudflare.jove.com/files/ftp_upload/56457/56457fig4large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 5" class="xfigimg" src="/files/ftp_upload/56457/56457fig5.jpg" /> 
Figure 5: Confirmation of TAT-Cx43266-283-B intracellular interactions in G166 GSCs by confocal microscopy. 
G166 GSCs were incubated with 50 &#181;M TAT-Cx43266-283-B. After 30 min, cells were fixed and processed to localize TAT-Cx43266-283-B with Cy2-Streptavidin (green), c-Src by immunofluorescence (red) and phosphatidylserine with annexin V (blue). Note some points of co-localization (white) between TAT-Cx43266-283-B and c-Src close to the plasma membrane in the merge images. <a href="https://cloudflare.jove.com/files/ftp_upload/56457/56457fig5large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>

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Biotinylated Cell-penetrating Peptides to Study Intracellular Protein-protein Interactions

This is a protocol to study intracellular protein-protein interactions based on the biotin-avidin pull-down system with the novelty of combining cell-penetrating sequences. The main advantage is that the target sequence is incubated with living cells instead of cell lysates and therefore the interactions will occur within the cellular context.

Here we present a protocol to study intracellular protein-protein interactions that is based on the widely used biotin-avidin pull-down system. The ...

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9.4K Views.  Universidad de Salamanca. This is a protocol to study intracellular protein-protein interactions based on the biotin-avidin pull-down system with the novelty of combining cell-penetrating sequences. The main advantage is that the target sequence is incubated with living cells instead of cell lysates and therefore the interactions will occur within the cellular context.

Video: Biotinylated Cell-penetrating Peptides to Study Intracellular Protein-protein Interactions

Split-BioID &#8212; Proteomic Analysis of Context-specific Protein Complexes in Their Native Cellular Environment

To complement existing affinity purification (AP) approaches for the identification of protein-protein interactions (PPI), enzymes have been introduced that allow the proximity-dependent labeling of proteins in living cells. One such enzyme, BirA* (used in the BioID approach), mediates the biotinylation of proteins within a range of approximately 10 nm. Hence, when fused to a protein of interest and expressed in cells, it allows the labeling of proximal proteins in their native environment. As opposed to AP that relies on the purification of assembled protein complexes, BioID detects proteins that have been marked within cells no matter whether they are still interacting with the protein of interest when they are isolated. Since it biotinylates proximal proteins, one can moreover capitalize on the exceptional affinity of streptavidin for biotin to very efficiently isolate them. While BioID performs better than AP for identifying transient or weak interactions, both AP- and BioID-mass spectrometry approaches provide an overview of all possible interactions a given protein may have. However, they do not provide information on the context of each identified PPI. Indeed, most proteins are typically part of several complexes, corresponding to distinct maturation steps or different functional units. To address this common limitation of both methods, we have engineered a protein-fragments complementation assay based on the BirA* enzyme. In this assay, two inactive fragments of BirA* can reassemble into an active enzyme when brought in close proximity by two interacting proteins to which they are fused. The resulting split-BioID assay thus allows the labeling of proteins that assemble around a pair of interacting proteins. Provided these two only interact in a given context, split-BioID then allows the analysis of specific context-dependent functional units in their native cellular environment. Here, we provide a step-by-step protocol to test and apply split-BioID to a pair of interacting proteins.

We provide a step-by-step protocol for split-BioID, a protein fragments-complementation assay based on the proximity-labeling technique BioID. Activated on the interaction of two given proteins, it allows the proteomics analysis of context-dependent protein complexes in their native cellular environment. The method is simple, cost-effective and only requires standard laboratory equipment.

To complement existing affinity purification (AP) approaches for the identification of protein-protein interactions (PPI), enzymes have been introduced ...

Fluorescent Leakage Assay to Investigate Membrane Destabilization by Cell-Penetrating Peptide

Cell-penetrating peptides (CPPs) are defined as carriers that are able to cross the plasma membrane and to transfer a cargo into cells. One of the main common features required for this activity resulted from the interactions of CPPs with the plasma membrane (lipids) and more particularly with components of the extracellular matrix of the membrane itself (heparan sulphate). Indeed, independent of the direct translocation or the endocytosis-dependent internalization, lipid bilayers are involved in the internalization process both at the level of the plasma membrane and at the level of intracellular traffic (endosomal vesicles). In this article, we present a detailed protocol describing the different steps of a large unilamellar vesicles (LUVs) formulation, purification, characterization, and application in fluorescence leakage assay in order to detect possible CPP-membrane destabilization/interaction and to address their role in the internalization mechanism. LUVs with a lipid composition reflecting the plasma membrane content are generated in order to encapsulate both a fluorescent dye and a quencher. The addition of peptides in the extravesicular medium and the induction of peptide-membrane interactions on the LUVs might thus induce in a dose-dependent manner a significant increase in fluorescence revealing a leakage. Examples are provided here with the recently developed tryptophan (W)- and arginine (R)-rich Amphipathic Peptides (WRAPs), which showed a rapid and efficient siRNA delivery in various cell lines. Finally, the nature of these interactions and the affinity for lipids are discussed to understand and to improve the membrane translocation and/or the endosomal escape.

The fluorescence leakage assay is a simple method that enables the investigation of peptide/membrane interactions in order to understand their involvement in several biological processes and especially the ability of cell-penetrating peptides to disturb phospholipids bilayers during a direct cellular translocation process.

Cell-penetrating peptides (CPPs) are defined as carriers that are able to cross the plasma membrane and to transfer a cargo into cells. One of the main ...

In-vivo Detection of Protein-protein Interactions on Micro-patterned Surfaces

Unraveling the interaction network of molecules in-vivo is key to understanding the mechanisms that regulate cell function and metabolism. A multitude of methodological options for addressing molecular interactions in cells have been developed, but most of these methods suffer from being rather indirect and therefore hardly quantitative. On the contrary, a few high-end quantitative approaches were introduced, which however are difficult to extend to high throughput. To combine high throughput capabilities with the possibility to extract quantitative information, we recently developed a new concept for identifying protein-protein interactions (Schwarzenbacher et al., 2008). Here, we describe a detailed protocol for the design and the construction of this system which allows for analyzing interactions between a fluorophore-labeled protein ("prey") and a membrane protein ("bait") in-vivo. Cells are plated on micropatterned surfaces functionalized with antibodies against the bait exoplasmic domain. Bait-prey interactions are assayed via the redistribution of the fluorescent prey. The method is characterized by high sensitivity down to the level of single molecules, the capability to detect weak interactions, and high throughput capability, making it applicable as screening tool.

In-vivo Detection of Protein-protein Interactions on Micro-patterned Surfaces

This video shows experiments with subsequent analysis of protein-protein interactions by the use of micro-patterned surfaces. The approach offers the possibility to detect protein interactions in living cells and combines high throughput capabilities with the possibility to extract quantitative information.

Unraveling the interaction network of molecules in-vivo is key to understanding the mechanisms that regulate cell function and metabolism. A multitude of ...

Biology

Construction of Cyclic Cell-Penetrating Peptides for Enhanced Penetration of Biological Barriers

Cancer has been a grand challenge in global health. However, the complex tumor microenvironment generally limits the access of therapeutics to deeper tumor cells, leading to tumor recurrence. To conquer the limited penetration of biological barriers, cell-penetrating peptides (CPPs) have been discovered with excellent membrane translocation ability and have emerged as useful molecular transporters for delivering various cargoes into cells. However, conventional linear CPPs generally show compromised proteolytic stability, which limits their permeability across biological barriers. Thus, the development of novel molecular transporters that can penetrate biological barriers and exhibit enhanced proteolytic stability is highly desired to promote drug delivery efficiency in biomedical applications. We have previously synthesized a panel of short cyclic CPPs with aromatic crosslinks, which exhibited superior permeability in cancer cells and tissues compared to their linear counterparts. Here, a concise protocol is described for the synthesis of the fluorescently labeled cyclic polyarginine R8 peptide and its linear counterpart, as well as key steps for investigating their cell permeability.

This protocol describes the synthesis of cyclic cell-penetrating peptides with aromatic cross-links and the evaluation of their permeability across biological barriers.

Cancer has been a grand challenge in global health. However, the complex tumor microenvironment generally limits the access of therapeutics to deeper ...

Chemistry

Measuring Peptide Translocation into Large Unilamellar Vesicles

There is an active interest in peptides that readily cross cell membranes without the assistance of cell membrane receptors1. Many of these are referred to as cell-penetrating peptides, which are frequently noted for their potential as drug delivery vectors1-3. Moreover, there is increasing interest in antimicrobial peptides that operate via non-membrane lytic mechanisms4,5, particularly those that cross bacterial membranes without causing cell lysis and kill cells by interfering with intracellular processes6,7. In fact, authors have increasingly pointed out the relationship between cell-penetrating and antimicrobial peptides1,8. A firm understanding of the process of membrane translocation and the relationship between peptide structure and its ability to translocate requires effective, reproducible assays for translocation. Several groups have proposed methods to measure translocation into large unilamellar lipid vesicles (LUVs)9-13. LUVs serve as useful models for bacterial and eukaryotic cell membranes and are frequently used in peptide fluorescent studies14,15. Here, we describe our application of the method first developed by Matsuzaki and co-workers to consider antimicrobial peptides, such as magainin and buforin II16,17. In addition to providing our protocol for this method, we also present a straightforward approach to data analysis that quantifies translocation ability using this assay. The advantages of this translocation assay compared to others are that it has the potential to provide information about the rate of membrane translocation and does not require the addition of a fluorescent label, which can alter peptide properties18, to tryptophan-containing peptides. Briefly, translocation ability into lipid vesicles is measured as a function of the Foster Resonance Energy Transfer (FRET) between native tryptophan residues and dansyl phosphatidylethanolamine when proteins are associated with the external LUV membrane (Figure 1). Cell-penetrating peptides are cleaved as they encounter uninhibited trypsin encapsulated with the LUVs, leading to disassociation from the LUV membrane and a drop in FRET signal. The drop in FRET signal observed for a translocating peptide is significantly greater than that observed for the same peptide when the LUVs contain both trypsin and trypsin inhibitor, or when a peptide that does not spontaneously cross lipid membranes is exposed to trypsin-containing LUVs. This change in fluorescence provides a direct quantification of peptide translocation over time.

This protocol details a method for the quantitative measure of peptide translocation into large unilamellar lipid vesicles. This method also provides information about the rate of membrane translocation and can be used to identify peptides that efficiently and spontaneously cross lipid bilayers.

There is an active interest in peptides that readily cross cell membranes without the assistance of cell membrane receptors1.  Many of these are referred ...

Identifying Protein-protein Interaction Sites Using Peptide Arrays

Protein-protein interactions mediate most of the processes in the living cell and control homeostasis of the organism. Impaired protein interactions may result in disease, making protein interactions important drug targets. It is thus highly important to understand these interactions at the molecular level. Protein interactions are studied using a variety of techniques ranging from cellular and biochemical assays to quantitative biophysical assays, and these may be performed either with full-length proteins, with protein domains or with peptides. Peptides serve as excellent tools to study protein interactions since peptides can be easily synthesized and allow the focusing on specific interaction sites. Peptide arrays enable the identification of the interaction sites between two proteins as well as screening for peptides that bind the target protein for therapeutic purposes. They also allow high throughput SAR studies. For identification of binding sites, a typical peptide array usually contains partly overlapping 10-20 residues peptides derived from the full sequences of one or more partner proteins of the desired target protein. Screening the array for binding the target protein reveals the binding peptides, corresponding to the binding sites in the partner proteins, in an easy and fast method using only small amount of protein.
In this article we describe a protocol for screening peptide arrays for mapping the interaction sites between a target protein and its partners. The peptide array is designed based on the sequences of the partner proteins taking into account their secondary structures. The arrays used in this protocol were Celluspots arrays prepared by INTAVIS Bioanalytical Instruments. The array is blocked to prevent unspecific binding and then incubated with the studied protein. Detection using an antibody reveals the binding peptides corresponding to the specific interaction sites between the proteins.

Peptide array screening is a high throughput assay for identifying protein-protein interaction sites. This allows mapping multiple interactions of a target protein and can serve as a method for identifying sites for inhibitors that target a protein. Here we describe a protocol for screening and analyzing peptide arrays.

Protein-protein interactions mediate most of the processes in the living cell and control homeostasis of the organism. Impaired protein interactions may ...

In Vivo Imaging of Transduction Efficiencies of Cardiac Targeting Peptide

Since the initial description of protein transduction domains, also known as cell penetrating peptides, over 25 years ago, there has been intense interest in developing these peptides, especially cell-specific ones, as novel vectors for delivering diagnostic and therapeutic materials. Our past work involving phage display identified a novel, nonnaturally occurring, 12 amino acid-long peptide that we named cardiac targeting peptide (CTP) due to its ability to transduce normal heart tissue in vivo with peak uptake seen in as little as 15 min after an intravenous injection. We have undertaken detailed biodistribution studies by injecting CTP labeled with fluorophore cyanine5.5, allowing it to circulate for various periods of time, and euthanizing, fixing, and sectioning multiple organs followed by fluorescent microscopy imaging. In this publication, we describe these processes as well as ex vivo imaging of harvested organs using an in vivo imaging system in detail. We provide detailed methodologies and practices for undertaking transduction as well as biodistribution studies using CTP as an example.

We describe protocols for assessing the degree of transduction by cell-penetrating peptides utilizing ex vivo imaging systems followed by paraffin embedding, sectioning, and confocal fluorescent microscopy using cardiac targeting peptide as an example. In our protocol, a single animal can be used to acquire both types of imaging assessment of the same organs, thereby cutting the number of animals needed for studies by half.

Since the initial description of protein transduction domains, also known as cell penetrating peptides, over 25 years ago, there has been intense interest ...

Live Cell Single-Molecule Imaging-Based Quantification of Protein Interactions

Single-Molecule Measurement of Protein Interaction Dynamics Within Biomolecular Condensates

Biomolecular condensates formed via liquid-liquid phase separation (LLPS) have been considered critical in cellular organization and an increasing number of cellular functions. Characterizing LLPS in live cells is also important because aberrant condensation has been linked to numerous diseases, including cancers and neurodegenerative disorders. LLPS is often driven by selective, transient, and multivalent interactions between intrinsically disordered proteins. Of great interest are the interaction dynamics of proteins participating in LLPS, which are well-summarized by measurements of their binding residence time (RT), that is, the amount of time they spend bound within condensates. Here, we present a method based on live-cell single-molecule imaging that allows us to measure the mean RT of a specific protein within condensates. We simultaneously visualize individual protein molecules and the condensates with which they associate, use single-particle tracking (SPT) to plot single-molecule trajectories, and then fit the trajectories to a model of protein-droplet binding to extract the mean RT of the protein. Finally, we show representative results where this single-molecule imaging method was applied to compare the mean RTs of a protein at its LLPS condensates when fused and unfused to an oligomerizing domain. This protocol is broadly applicable to measuring the interaction dynamics of any protein that participates in LLPS.

Author Spotlight: Evaluation of Protein-Condensate Dynamics in Live Human Cells

Many intrinsically disordered proteins have been shown to participate in the formation of highly dynamic biomolecular condensates, a behavior important for numerous cellular processes. Here, we present a single-molecule imaging-based method for quantifying the dynamics by which proteins interact with each other in biomolecular condensates in live cells.

Biomolecular condensates formed via liquid-liquid phase separation (LLPS) have been considered critical in cellular organization and an increasing number ...

Assessing the Internalization of  Target Surface Proteins Using a Biotin Derivative

Source: Tham, D. K. L., et al., <a href="https://app.jove.com/v/55974">Determining Cell-surface Expression and Endocytic Rate of Proteins in Primary Astrocyte Cultures Using Biotinylation.</a> J. Vis. Exp. (2017).
This video demonstrates a method to assess target protein internalization in the mouse cortical astrocytes using biotinylation, followed by cell lysis, streptavidin-based protein extraction, denaturation, and Western blot analysis to confirm successful internalization.

All procedures involving animal samples have been reviewed and approved by the appropriate animal ethical review committee.
1. Determining Internalization ...

JoVE Encyclopedia of Experiments

Neuroscience

Neuropathology

Epilepsy and Seizure Disorders

Biotinylated Cell-Penetrating Peptide Probe to Detect Protein-Protein Interactions

Source: Jara&#237;z-Rodr&#237;guez, M. et al., <a href="https://app.jove.com/v/56457">Biotinylated Cell-penetrating Peptides to Study Intracellular Protein-protein Interactions.</a> J. Vis. Exp. (2017).
This video demonstrates a technique that uses biotinylated cell-penetrating peptides to detect intracellular protein-protein interactions. The cell-penetrating peptides facilitate the conjugated peptide to enter a cell and specifically bind to its interacting proteins. The biotin, after binding to avidin, allows purification of the interacting proteins&#8217; complex from a cell lysate.

Source: Jara&#237;z-Rodr&#237;guez, M. et al., Biotinylated Cell-penetrating Peptides to Study Intracellular Protein-protein Interactions. J. Vis. Exp. ...

Biotinylated Cell-penetrating Peptides to Study Intracellular Protein-protein Interactions

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Chapters in this video

Split-BioID — Proteomic Analysis of Context-specific Protein Complexes in Their Native Cellular Environment

Fluorescent Leakage Assay to Investigate Membrane Destabilization by Cell-Penetrating Peptide

In-vivo Detection of Protein-protein Interactions on Micro-patterned Surfaces

Construction of Cyclic Cell-Penetrating Peptides for Enhanced Penetration of Biological Barriers

Measuring Peptide Translocation into Large Unilamellar Vesicles

Identifying Protein-protein Interaction Sites Using Peptide Arrays

In Vivo Imaging of Transduction Efficiencies of Cardiac Targeting Peptide

Single-Molecule Measurement of Protein Interaction Dynamics Within Biomolecular Condensates

Assessing the Internalization of Target Surface Proteins Using a Biotin Derivative

Biotinylated Cell-Penetrating Peptide Probe to Detect Protein-Protein Interactions