The authors would like to thank BESSY II, operated by Helmholtz-Zentrum Berlin for beam time access and support, and the departments of Sample Environment and Technical Design for their help with design and construction and the access to the 3D-printer facilities.

CAUTION: For all subsequent work, it is very important that the yellow-colored polyimide foil must not be touched with unprotected fingers, because of possible contaminations to the sample holder. Also, the usage of protected forceps is highly recommended.
1. The sample holder
<ol>
	<li>Use one of the three types of sample holder. 
	NOTE: Three different versions of the new developed sample holder are shown in Figure 1. All of them contain a black plastic support structure, an airtight COC foil on the outside and a microporous structured polyimide foil on the inside. Type 1 (Figure 1A) contains a fixed outer plastic ring, whereas for types 2 and 3 (Figure 1B,1C) the outer ring can be broken off mechanically at the designated respective break points for use in automated sample transfer systems (see red arrows in Figure 1B). The design of the sample holders allows the setup of multiple crystallization drops on the yellow polyimide foil. It does not compromise the monitoring of the crystallization experiment, as the material is highly transparent for visible light. The 21 &#956;m thick polyimide foil also features 5 &#956;m pores, which allows simple crystal manipulation by soaking later on. Since the transmission of X-rays is close to 1.0 at all commonly used diffraction data collection energies in macromolecular crystallography, the contribution of the foil to the background scattering in a diffraction experiment is negligible28.</li>
</ol>
2. Setting up crystallization drops
<ol>
	<li>Create a clean and dust-free surface using a damp lint-free cloth. Take one sample holder from its box and gently place it, yellow foil facing up, on the cleaned surface to avoid damage or unwanted puncture of the backside COC foil.</li>
	<li>Set up the crystallization drops with a maximum recommended volume of 2 &#181;L on the yellow foil as it would be done on commonly used cover slides. Place the drops gently to avoid any rupture or piercing of the foil using a pipette. On a sample holder of type 1 (Figure 2A) up to three drops can be placed, whereas on sample holders of type 2 and 3 two drops are the recommended maximum (Figure 2C).</li>
	<li>Flip the sample holder over and place it onto a pre-greased cavity of a 24-well Linbro style plate. Use the positioning aids (see red arrows in Figure 1A) of the sample holder to guide it to its optimal position.</li>
	<li>Ensure the correct position of the sample holder in order to avoid unwanted evaporation (Figure 2A).</li>
</ol>
3. Observing crystal growth
<ol>
	<li>By placing the crystallization plate under a transmission light microscope, with or without polarizers, monitor crystal growth without any disturbance of the experiment (Figure 4).</li>
	<li>When using the smaller 18-mm sample holders of type 3 (Figure 1C), which were designed for use on SBS footprint plates, use an imaging robot capable of handling SBS-footprint plates to monitor the crystal growth in a more automated way.</li>
</ol>
4. Crystal manipulation
NOTE: It is recommended to perform all subsequent steps under a transmission light microscope.
<ol>
	<li>Cryo-protection
	<ol>
		<li>Gently pierce the outer COC foil using a fine cannula. Make sure the inner yellow foil remains untouched. The puncture should be right next to the drop that is to be manipulated (Figure 3A,3C).</li>
		<li>Use a fine paper wick and insert it in the poked hole. Carefully push the wick forward until it touches the yellow polyimide foil. Keep the wick in contact with the perforated foil. The wick will suck away all excess solution. The time required for complete liquid removal depends on the viscosity of the solutions and the mother liquor composition (Figure 3B).</li>
		<li>After all liquid is sucked away, gently retract the paper wick. Remember the position of the drop, since it may not be visible after removal of the mother liquor.</li>
		<li>Take a standard pipette to apply a small volume of cryo-protectant solution, max. 3 &#181;L, using an extruded tip (e.g., a gel loading tip) through the same hole. Once the liquid is dispensed, retract the tip. The porosity of the yellow foil allows for diffusion across the foil. The time to attain cryo-protection of your crystals highly depends on the employed solution and its components.</li>
		<li>To reseal the self-healing COC foil, gently place a protected finger on the hole for about 1 s and slide it across the puncture. The slight pressure in combination with the elevated temperature will promote the resealing of punctures, which are not too large.</li>
	</ol>
	</li>
	<li>Ligand soaking 
	 
	NOTE: Excess mother liquor may be removed before ligand soaking. To do so, follow the steps described in 4.1.1 to 4.1.3.
	<ol>
		<li>Dissolve the ligand in mother liquor in the desired concentration in a reaction tube.</li>
		<li>Spin the solution for 10 minutes at 12,000 x g in order to remove insoluble particles. Use a temperature-controlled centrifuge if needed.</li>
		<li>Gently place a volume of max. 3 &#181;L of ligand containing solution in the gap between the COC foil and the polyimide film using a long, extruded pipet tip. Retract the tip.</li>
		<li>To reseal the self-healing COC foil, gently place a protected finger on the hole for about 1 s and slide it across the puncture (see also 4.1.5).</li>
		<li>Incubate the experiment for some time in order to allow for diffusion across the membrane. The soaking time highly depends on the viscosity of the diffusing solution and its components29.</li>
		<li>Repeat steps 4.2.1 to 4.2.5 multiple times to subsequently soak different ligands.</li>
	</ol>
	</li>
</ol>
5. In situ diffraction data collection at ambient temperature
NOTE: In order to minimize solvent scattering, remove excess solution before data collection.
<ol>
	<li>Ensure a stable humidity controlled beamline environment with pre-established conditions30.</li>
	<li>Gently lift the transparent COC foil at the designated point using forceps and peel it off like one would remove the lid from a yogurt cup ( Figure 6B).</li>
	<li>Gently lift the sample holder from its cavity and insert it immediately into a pre-prepared magnetic sample holder base. No glue is necessary for this step (Figure 6B).</li>
	<li>Apply gentle pressure to ensure the correct positioning of the sample holder within the base.</li>
	<li>Mount the sample holder on a beamline goniometer and ensure correct positioning of the holder. Depending on goniometer geometry the sample holder can be rotated by up to 160&#176; without causing any shadowing during the diffraction experiment.</li>
	<li>Use a paper wick and gently touch the yellow polyimide foil from the backside to remove excess mother liquor. Please note, that at that stage ligand soaking or cryo-protection may be performed just as well. The sample is now ready for centering and diffraction data collection.</li>
	<li>When using a sample holder with removable outer ring, apply gentle pressure by holding on to the outer ring and break it off at the designated break points (Figure 6C). The sample is now ready for centering and diffraction data collection.</li>
</ol>
6. In situ diffraction data collection at cryogenic temperature
NOTE: It is recommended to remove residual mother liquor from the sample by performing the steps 4.1.1. to 4.1.3. before continuing with the next steps to minimize solvent scattering. Most samples may be transferred to liquid nitrogen without prior cryo-protection31. If cryo-protection is needed, see steps 4.1.1. to 4.1.5.
<ol>
	<li>Gently lift the COC foil at the designated point using a forceps and peel it off (see step 5.1.2) (Figure 6A).</li>
	<li>Take the sample holder off the cavity and mount it on a magnetic sample holder base. Gentle pressure may be applied in order to ensure correct and tight fitting (see step 5.1.5, Figure 6B). 
	NOTE: The symmetrically arranged designated break points allow for simple removal of the outer ring of the sample holder by applying gentle pressure (see step 5.1.8., Figure 6C). Now, the sample holder is ready and can be plunged into liquid nitrogen. The geometry of the sample holder types 2 and 3 (Figure 1B,1C) allows their transfer into standard SPINE sample vials, which can be used for robot assisted sample mounting (Figure 6D).</li>
</ol>

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Patent applications regarding the reported sample holder have been filed by Helmholtz-Zentrum Berlin with the following registration numbers and registration dates with the German Patent and Trademark Office: DE 10 2018 129 125.6, registration date November 20th, 2018; DE 10 2018 125 129.7, registration date October 11th, 2018; DE 10 2017 129 761.8, registration date December 13th, 2017. A subsequent international patent application via the PCT route, using the priority of DE 10 2017 129 761.8 has been filed, PCT/DE2018/101007. A registration of a utility model with the number DE 20 2018 106 955.1 was filed on December 6th, 2018. The sample holder has been made commercially available under the trade names XtalTool and XtalTool/HT by Jena Bioscience, Jena, Germany.

Suitability for crystallization experiments. The new sample holders can be used for standard hanging drop crystallization experiments using either 24-well Linbro type plates (types 1 and 2), or 24-well SBS footprint plates in which each well has a diameter of 18 mm (type 3). They can be used instead of the standard microscope cover slips. The amorphous COC foil ensures the airtightness of the system. The monitoring of the crystallization experiment is possible using a transmission light microscope, because of the use of high clarity foils. To the best of our knowledge, no other sample holders exist for 24-well crystallization plates, which would allow crystal manipulation or diffraction experiments, without mechanically removing the crystal from the drop, in which it is grown. This is of particular importance, since many researchers in the field still rely on such plates for crystal optimization, due to the fact that larger drop volumes can be used compared to 96-well sitting-drop plates. With these larger drop volumes, larger crystals may be obtained.
Suitability for crystal manipulation. Due to the self-healing properties of the outer COC foil and the microporous structure of the inner yellow polyimide foil, the crystal environment is accessible and the crystals can be manipulated without mechanically transferring them to other containers. This makes the sample holders very convenient. The only other system we know of, which allows this indirect and gentle access to the crystal, is the CrystalDirect system26. However, CrystalDirect is less flexible since special 96-well crystallization plates have to be used. The foil, on which the crystals are growing, is the same that seals the crystallization experiment and it is not self-healing. This means that an aperture that has been pierced into the foil by laser ablation for ligand or cryo-protectant delivery to the crystals will remain open, increasing the chance for liquid evaporation. This is&#160;in contrast to our design, where&#160;crystals will not be directly exposed to the environment even if the COC foil gets pierced a number of times.
Suitability for in situ diffraction experiments at ambient temperature. The sample holder can be removed from the crystallization plate in a straight-forward manner, stuck onto a magnetic base and put on a beamline goniometer. For a diffraction experiment at room temperature, it is advisable to put the sample into an air stream of defined humidity33. The mother liquor around the crystal may be removed prior to putting the sample holder on the goniometer in order to reduce the background scattering. Such a set-up is stable for hours.
Suitability of the used material for operation and storage at 100 K. Neither the material used for the production of the sample holder nor the polyimide film are adversely affected by cooling them down to low temperatures34. Hence, working with the sample holder at low temperature (e.g., 100 K) does not pose a serious problem.
Suitability for in situ diffraction experiments at 100 K. For data collection at 100 K in a nitrogen stream, the sample holder needs to be removed from the crystallization plate as in the previous paragraph, stuck onto a magnetic base and put into a gaseous nitrogen stream at 100 K on a beamline goniometer. If desired, the sample may also be cryo-protected, although it is likely that for naked samples this may not be necessary in most cases31. For experiments at 100 K, the sample holders type 2 and 3 are better suited because the outer plastic ring can be removed. Hence, they are of smaller size and should therefore be less prone to icing. However, even a sample holder of type 1 may be used. Given a not too high humidity in the experimental hutch and a properly aligned cryo-system icing up of the holder is not really a problem.
Limitations. The sample holder&#39;s geometry permits unobstructed diffraction data collection by the rotation method over a total rotation range of 160&#176;. This is sufficient so that complete diffraction data sets can be obtained for most crystal systems. In cases where this is not possible, data from more than crystal need to be merged together. When crystals are grown together, it may be possible to adjust the size of the incident X-ray beam so that only parts of individual crystals are exposed. In extreme cases, one may need to resort to a data collection strategy similar to the MeshAndCollect approach35. In summary, while there are certain limitations associated with the sample holders, these can be overcome in most cases. Of course, it is always possible that situations are encountered, in which none of this is possible. In such cases, one may need to resort to other crystal mounting methods.
We have described a novel type of sample holder for macromolecular crystallography and we have demonstrated the suitability of the sample holders for various applications. Taking into account the simple and reproducible handling of protein crystals, as well as the unique properties of the sample holders, we believe that these sample holders will prove to be a valuable addition to the arsenal of sample holders for macromolecular crystallography.

The knowledge of the three-dimensional structure of biological macromolecules constitutes an important cornerstone in all basic biological, biochemical and biomedical research. This even extends to certain translational aspects of such research, such as for instance drug discovery. Among all methods for obtaining such three-dimensional information at atomic resolution X-ray crystallography is the most powerful and the most prominent one as is evidenced by the fact that 90% of all available structural information is contributed by X-ray crystallography1. The major prerequisite of X-ray crystallography, which is at the same time its major limitation, is that diffraction-quality crystals have to be produced and prepared for the diffraction experiment. This step still constitutes one of the major bottlenecks of the method.
Historically, diffraction data from protein crystals were collected at ambient temperature. Individual crystals were carefully transferred into glass or quartz capillaries prior to data collection, mother liquor was added to the capillaries so that the crystals would not dry out and the capillaries were sealed2,3,4. Since the 1980s, it became more and more apparent that due to the ionizing properties of X-radiation and the imminent radiation sensitivity of macromolecular crystals, data collection at ambient temperature poses severe limitations on the method. Consequently, approaches were developed to mitigate radiation damage effects by cooling macromolecular crystals down to 100 K and to collect diffraction data at such low temperature5,6. For working at low temperatures, the mounting of the samples in capillaries became impractical due to the low rate of heat transfer. In spite of this, there are ongoing efforts to also use capillaries, in particular from counter-diffusion crystallization experiments, for low-temperature diffraction work7,8, but, irrespective of that, it became the standard approach in macromolecular crystallography to mount macromolecular crystals held by a thin film of mother liquor inside a thin wired loop9,10. Even though a number of improvements (e.g., the introduction of lithographic loops and similar structures11) have been made over time to this loop-based mounting, the basic principles that were developed in the early 1990s are still in use today. It may be safely stated that most diffraction data collections on macromolecular crystals nowadays still rely on this approach5.
Over time, there were some interesting new developments and modifications of the loop-based mounting method, but these approaches have so far not been widely adopted in the community. One is the so-called loop-less mounting of crystals, which was developed to achieve lower background scattering12,13,14. Another one is the use of graphene sheaths to wrap the crystalline samples and to protect them from drying out. Graphene is a well-suited material in that respect because of its very low X-ray scattering background15.
More recently, developments in the field of sample mounts were mainly focused on standardizing the mounts with the aim of increasing sample throughput16 or on designing mounts, which can hold more than one sample17, such as for instance patterned membranes on a silicon frame, which are capable of holding hundreds of small crystals mostly in the field of serial crystallography18,19,20,21,22.
All of the sample mounting methods discussed so far still require some degree of manual intervention, which means that there is an inherent danger of causing mechanical damage to the sample. Therefore, novel approaches are being sought by engineering the sample environment such that diffraction data of crystals can be collected within their growth environment. One such method is termed in situ or plate-screening23,24 and it is already implemented at a number of macromolecular crystallography beamlines at various synchrotron sources worldwide25. However, the use of this method is limited by the geometrical parameters of the crystal plate and the space available around the sample point of the instrument.
Yet another approach is realized in the so-called CrystalDirect system26. Here, entire crystallization drops are harvested automatically. The foils on which the crystals have been grown are custom-cut using a laser and directly used as the sample holder27.
In the work described here, the aim was to develop a sample holder, which would allow a user to move the crystalline sample from its growth chamber to the data collection device without touching it and which would enable the user to manipulate the sample easily. Since many researchers in the field of macromolecular crystallography are still using the 24-well crystallization format for optimizing crystal growth by modifying conditions identified in large screening campaigns, the new sample holder was designed to be compatible with this format. In the following, the design of the new sample holder will be described and the handling and the performance of the sample holder for in situ data collection and ligand soaking will be demonstrated. Finally, the suitability of this new sample holder as well as its limitations for the various work steps will be discussed.

<table border="0" cellpadding="0" cellspacing="0" style="width:1167px;" width="1167">
	<tbody>
		<tr height="21">
			<td height="21" style="height:21px;width:221px;">AF Satetiss</td>
			<td style="width:253px;">RS Components</td>
			<td style="width:207px;">101-5738</td>
			<td style="width:485px;">lint-free paper, multiple retailer</td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;width:221px;">Cannula</td>
			<td style="width:253px;">Dispomed Neoject</td>
			<td style="width:207px;">25 G 5/8&#34; 0.5 x 16, Ref:10026</td>
			<td>multiple retailer</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:221px;">COC foil</td>
			<td style="width:253px;">HJ-Bioanalytik GmbH</td>
			<td style="width:207px;">900360</td>
			<td></td>
		</tr>
		<tr height="24">
			<td height="24" style="height:24px;width:221px;">ComboPlate</td>
			<td style="width:253px;">Greiner Bio-one / Jena Bioscience</td>
			<td style="width:207px;">662050 / CPL-131</td>
			<td>pre-greased plate, multiple retailer</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:221px;">Cryo Vials</td>
			<td style="width:253px;">Jena Bioscience</td>
			<td style="width:207px;">CV-100</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:221px;">Eppendorf Research Plus&#160;</td>
			<td style="width:253px;">Eppendorf</td>
			<td style="width:207px;">3123000012</td>
			<td>0.1 - 2.5 &#181;L volume</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:221px;">Eppendorf Tubes</td>
			<td style="width:253px;">Eppendorf</td>
			<td style="width:207px;">30125150</td>
			<td>1.5 mL g-Safe Eppendorf Quality, manufacturer reference number</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:221px;">Forceps Usbeck</td>
			<td style="width:253px;">FisherScientific</td>
			<td style="width:207px;">10750313</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:221px;">GELoader Eppendorf Quality</td>
			<td style="width:253px;">Eppendorf</td>
			<td style="width:207px;">30001222</td>
			<td>extruded&#160; tips (0.2 - 20 &#181;L), manufacturer reference number</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:221px;">Magnetic CryoVials</td>
			<td style="width:253px;">Molecular Dimension</td>
			<td style="width:207px;">MD7-402</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:221px;">Microfuge Thermo</td>
			<td style="width:253px;">ThermoFisher Scientific</td>
			<td style="width:207px;">R21</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:221px;">Paper wicks</td>
			<td style="width:253px;">dental2000</td>
			<td style="width:207px;">64460</td>
			<td>Set of paper wicks, multiple retailer</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:221px;">Rotiprotect Nitril-eco&#160;</td>
			<td style="width:253px;">Carl Roth</td>
			<td style="width:207px;">TC14.1</td>
			<td>powder free, multiple retailer</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:221px;">SuperClear Plates</td>
			<td style="width:253px;">Jena Bioscience</td>
			<td style="width:207px;">CPL-132</td>
			<td>pre-greased plate</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:221px;">UHU super glue</td>
			<td style="width:253px;">UHU GmbH &#38; Co KG</td>
			<td style="width:207px;">45545</td>
			<td>manufacturer reference number, multiple retailer</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:221px;">VeroBlackPlus</td>
			<td style="width:253px;">Alphacam</td>
			<td style="width:207px;">OBJ-40963</td>
			<td>manufacturer reference number</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:221px;">XtalTool&#160;</td>
			<td style="width:253px;">Jena Bioscience</td>
			<td style="width:207px;">X-XT-101</td>
			<td>sample holder set</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:221px;">XtalTool HT</td>
			<td style="width:253px;">Jena Bioscience</td>
			<td style="width:207px;">X-XT-103 / X-XT-104</td>
			<td>SPINE compatible sample holder set</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:221px;">XtalToolBases</td>
			<td style="width:253px;">Jena Bioscience</td>
			<td style="width:207px;">X-XT-105</td>
			<td>Magnetic sample holder bases set</td>
		</tr>
	</tbody>
</table>

an all-in-one sample holder for macromolecular x-ray crystallography with minimal background scattering

Macromolecular X-ray crystallography (MX) is the most prominent method to obtain high-resolution three-dimensional knowledge of biological macromolecules. A prerequisite for the method is that highly ordered crystalline specimen need to be grown from the macromolecule to be studied, which then need to be prepared for the diffraction experiment. This preparation procedure typically involves removal of the crystal from the solution, in which it was grown, soaking of the crystal in ligand solution or cryo-protectant solution and then immobilizing the crystal on a mount suitable for the experiment. A serious problem for this procedure is that macromolecular crystals are often mechanically unstable and rather fragile. Consequently, the handling of such fragile crystals can easily become a bottleneck in a structure determination attempt. Any mechanical force applied to such delicate crystals may disturb the regular packing of the molecules and may lead to a loss of diffraction power of the crystals. Here, we present a novel all-in-one sample holder, which has been developed in order to minimize the handling steps of crystals and hence to maximize the success rate of the structure determination experiment. The sample holder supports the setup of crystal drops by replacing the commonly used microscope cover slips. Further, it allows in-place crystal manipulation such as ligand soaking, cryo-protection and complex formation without any opening of the crystallization cavity and without crystal handling. Finally, the sample holder has been designed in order to enable the collection of in situ X-ray diffraction data at both, ambient and cryogenic temperature. By using this sample holder, the chances to damage the crystal on its way from crystallization to diffraction data collection are considerably reduced since direct crystal handling is no longer required.

The sample holder type 1 has been designed so that it fits onto a well of a 24-well Linbro style plate. Each individual sample holder contains positioning aids on either side of the outer rim in order to ensure optimal positioning on the rim of the well (Figure 1A, Figure 2A). Up to three individual crystallization drops of maximum volume 2 &#181;L each can be placed onto the yellow polyimide foil (Figure 2B). For sample holders of types 2 and 3, it is recommended to set a maximum of two drops of maximum volume 2 &#181;L each. 24 sample holders can be fitted onto one 24-well Linbro plate (Figure 3D).
A crystallization experiment on a 24-well Linbro plate using sample holder type 1 was set up. 1 &#181;L of hen egg-white lysozyme solution (15 mg/mL) was mixed with 1 &#181;L of mother-liquor comprising 50 mM NaAc pH 4.7, 500 mM NaCl and 25% (w/v) PEG-6000 on the yellow polyimide foil on the sample holder (Table 1). The drop was equilibrated at 293 K against 500 &#181;L of mother-liquor and crystals of the size 40-50 &#181;m were observed after 5 hours (Figure 4). Crystal growth can be observed using a transmission light microscope (Figure 4) with or without a polarizer. High transparency films ensure best observation and monitoring of crystal growing conditions using both, a conventional light microscope or an automated crystal imaging system. Crystal growth observation using UV-light was not tested.
After removing the mother liquor from around the crystals, a sample holder with hen egg-white lysozyme crystals was taken from the crystallization plate and placed in a humidity-controlled airstream on HZB-MX beamline 14.332. Diffraction data were collected at ambient temperature in 1&#176;-increments using a 150 &#956;m beam at 13.8 keV energy with 4 x 1010 photons/s and an exposure time of 5 s per image. A typical diffraction image is shown in Figure 5. No elevated background scattering on the diffraction image can be detected. Further experimental details as well as associated data processing statistics are listed in Table 2.
<img alt="Figure 1" class="xfigimg" src="/files/ftp_upload/59722/59722fig1.jpg" /> 
Figure 1: Schematic view of the new sample holders. The sample holders consist of a black plastic support, which is covered on the outer side with an amorphous cyclic olefin copolymer (COC) foil. This foil (colored in blue) is highly transparent and self-healing. It also ensures gas tightness of the experiment. The inner foil (colored in yellow) is made of bio-inert polyimide, which is highly transparent for X-rays. On this foil, the crystallization drops can be placed.The outer rim of the sample holder contains two positioning aids indicated by the red arrow (panel A), which allows accurate placement of the sample holder on the individual pre-greased cavity of the crystallization plate. (A) Sample holder (type 1) with 22 mm diameter with a fixed external support ring. (B) Sample holder (type 2) with 22 mm diameter with removable external support ring. (C) Sample holder (type 3) with 18 mm diameter with removable external support ring. The latter two have been developed for using them in a high-throughput fashion with automated sample mounting robots using SPINE standard. The designated break points are highlighted by the red arrows in panel B. The black arrow in panel C indicates the positioning marker. The protruding pins at the outer perimeter of the yellow foil are necessary to align the polyimide foil during the production process. <a href="https://www.jove.com/files/ftp_upload/59722/59722fig1large.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/59722/59722fig2.jpg" /> 
Figure 2: The sample holder may be used on a 24-well Linbro plate in the same way as the commonly used microscope cover slips. It seals the cavity airtight. Positioning aids ensure the correct positioning of the sample holder on the cavity (red arrows in panel A). Up to three individual drops may be placed onto a type 1 sample holder (panel B), whereas the recommended maximum number of drops placed on a type 2 or 3 sample holder is two. The maximum recommended volume for each drop is 2 &#181;L. <a href="https://www.jove.com/files/ftp_upload/59722/59722fig2large.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/59722/59722fig3.jpg" /> 
Figure 3: 24 type 1 sample holders fit on a 24-well plate. The sample holders can be placed in two orientations on the 24-well plate as indicated (panel D). A cannula is used to pierce the back COC foil in order to remove excess liquor from a crystallization drop (panels A and C) by using a paper wick gently inserted in the same hole (panel B). <a href="https://www.jove.com/files/ftp_upload/59722/59722fig3large.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/59722/59722fig4.jpg" /> 
Figure 4:&#160;Image of hen egg-white lysozyme crystals observed through a transmission microscope equipped with a polarizer. Individual crystals are easily discriminated from precipitated protein solution. The crystals in this image are of an average size of 40 &#181;m x 50 &#181;m. <a href="https://www.jove.com/files/ftp_upload/59722/59722fig4large.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/59722/59722fig5.jpg" /> 
Figure 5: A typical X-ray diffraction image of a lysozyme crystal grown on the sample holder. Prior to exposure to X-rays all excess mother liquor was removed from around the crystal. Diffraction data were collected at ambient temperature on BL14.3 at the electron storage ring BESSY II32 using a humidity controlled sample environment with 97.5% relative humidity. No elevated background due to the sample holders can be observed. The dashed lines in the image indicate the resolution rings. <a href="https://www.jove.com/files/ftp_upload/59722/59722fig5large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 6" class="xfigimg" src="/files/ftp_upload/59722/59722fig6.jpg" /> 
Figure 6:&#160;The sample holder is prepared for diffraction data collection. First, the COC film is lifted gently by using a forceps and then peeled off (panel A). Subsequently, the sample holder is removed from the cavity and inserted into the central hole of a magnetic base until indicated by the marker (panel B). By holding on to the central part, gentle pressure is applied to the outer ring to free the central part using the symmetrically arranged designated break points (panel C). After the removal, the sample holder can be plunged into liquid nitrogen and transferred into standard SPINE vials. Placed, for instance, in pucks they can be transported to synchrotron sites where automated sample-mounting robots recognize them as regular samples (panel D). <a href="https://www.jove.com/files/ftp_upload/59722/59722fig6large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>Crystallization details</td>
			<td></td>
		</tr>
		<tr>
			<td>Method</td>
			<td>Hanging drop, vapor diffusion method</td>
		</tr>
		<tr>
			<td>Plate type</td>
			<td>SuperClear Plates</td>
		</tr>
		<tr>
			<td>Temperature (K)</td>
			<td>293</td>
		</tr>
		<tr>
			<td>Protein concentration (mg mL-1)</td>
			<td>15</td>
		</tr>
		<tr>
			<td>Composition of reservoir solution</td>
			<td>50 mM NaAc pH 4.7, 500 mM NaCl, 25 % (w/v) PEG-6000</td>
		</tr>
		<tr>
			<td>Volume and ratio of drop</td>
			<td>2 &#181;L total, 1:1 ratio (protein : mother liquor</td>
		</tr>
		<tr>
			<td>Volume of reservoir</td>
			<td>500 &#181;L</td>
		</tr>
		<tr>
			<td>Incubation time</td>
			<td>12 hours</td>
		</tr>
	</tbody>
</table>
Table 1: Experimental details of the described crystallization experiment. 
<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>Data collection and processing</td>
			<td></td>
		</tr>
		<tr>
			<td>Wavelength (&#197;)</td>
			<td>0.89429</td>
		</tr>
		<tr>
			<td>Temperature (K)</td>
			<td>293</td>
		</tr>
		<tr>
			<td>Detector</td>
			<td>Rayonix MX225 CCD&#160;</td>
		</tr>
		<tr>
			<td>Crystal-detector distance (mm)</td>
			<td>120</td>
		</tr>
		<tr>
			<td>Rotation range per image (&#176;)</td>
			<td>0.5</td>
		</tr>
		<tr>
			<td>Total rotation range (&#176;)</td>
			<td>120</td>
		</tr>
		<tr>
			<td>Exposure time per image (s)</td>
			<td>5</td>
		</tr>
		<tr>
			<td>Space group&#160;</td>
			<td>P43212</td>
		</tr>
		<tr>
			<td>Unit-cell parameters (&#197;)</td>
			<td>a = 79.01, b = 79.01, c = 37.95</td>
		</tr>
		<tr>
			<td>Mosacity (&#176;)</td>
			<td>0.07</td>
		</tr>
		<tr>
			<td>Resolution range (&#197;)</td>
			<td>39.50 - 1.35 (1.37 - 1.35)</td>
		</tr>
		<tr>
			<td>Total number of reflections</td>
			<td>191940 (8932)</td>
		</tr>
		<tr>
			<td>Number of unique reflections</td>
			<td>27020 (1292)</td>
		</tr>
		<tr>
			<td>Completeness (%)</td>
			<td>99.88 (99.20)</td>
		</tr>
		<tr>
			<td>Multiplicity</td>
			<td>7.1 (6.9)</td>
		</tr>
		<tr>
			<td>Mean I/&#963;(I)</td>
			<td>15.0 (1.9)</td>
		</tr>
		<tr>
			<td>Rmeas35 (%)</td>
			<td>6.3 (107.0)</td>
		</tr>
		<tr>
			<td>Rpim36 (%)</td>
			<td>2.4 (40.4)</td>
		</tr>
		<tr>
			<td>CC1/237&#160;</td>
			<td>99.9 (68.5)</td>
		</tr>
		<tr>
			<td>ISa38</td>
			<td>&#160;16.1</td>
		</tr>
		<tr>
			<td>Wilson B-factor (&#197;2)</td>
			<td>17.0</td>
		</tr>
	</tbody>
</table>
Table 2: Diffraction data collection and processing statistics.

Watch this Scientific Journal Video about An All-in-one Sample Holder for Macromolecular X-ray Crystallography with Minimal Background Scattering at JoVE.com

An All-in-one Sample Holder for Macromolecular X-ray Crystallography with Minimal Background Scattering

Un porte-échantillon tout-en-un pour la cristallographie macromoléculaire de rayon X avec la diffusion minimale de fond

A novel sample holder for macromolecular X-ray crystallography along with a suitable handling protocol is presented. The system allows crystal growth, crystal soaking and in situ diffraction data collection at both, ambient and cryogenic temperature without the need of any crystal manipulation or mounting.

Macromolecular X-ray crystallography (MX) is the most prominent method to obtain high-resolution three-dimensional knowledge of biological macromolecules. ...

an-all-one-sample-holder-for-macromolecular-x-ray-crystallography

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Biochemistry

13.0K vues.  Helmholtz-Zentrum Berlin. Ce support d’échantillon peut être utilisé pour la culture de cristaux et la collecte de données de diffraction des rayons X. Ce porte-échantillon a été utilisé sur des plaques de 24 puits qui sont largement utilisées dans la communauté MX. L’aspect très important est qu’il n’y a pas de manipulation nécessaire.Un porte-échantillon comportant ces aspects décrits ici n’existait pas auparavant. Voir quelque chose est toujours beaucoup mieux que de simplement lire ?...

Vidéo: An All-in-one Sample Holder for Macromolecular X-ray Crystallography with Minimal Background Scattering

Simple Elimination of Background Fluorescence in Formalin-Fixed Human Brain Tissue for Immunofluorescence Microscopy

Immunofluorescence is a common method used to visualize subcellular compartments and to determine the localization of specific proteins within a tissue sample. A great hindrance to the acquisition of high quality immunofluorescence images is endogenous autofluorescence of the tissue caused by aging pigments such as lipofuscin or by common sample preparation processes such as aldehyde fixation. This protocol describes how background fluorescence can be greatly reduced through photobleaching using white phosphor light emitting diode (LED) arrays prior to treatment with fluorescent probes. The broad-spectrum emission of white phosphor LEDs allow for bleaching of fluorophores across a range of emission peaks. The photobleaching apparatus can be constructed from off-the-shelf components at very low cost and offers an accessible alternative to commercially available chemical quenchers. A photobleaching pre-treatment of the tissue followed by conventional immunofluorescence staining generates images free of background autofluorescence. Compared to established chemical quenchers which reduced probe as well as background signals, photobleaching treatment had no effect on probe fluorescence intensity while it effectively reduced background and lipofuscin fluorescence. Although photobleaching requires more time for pre-treatment, higher intensity LED arrays may be used to reduce photobleaching time. This simple method can potentially be applied to a variety of tissues, particularly postmitotic tissues that accumulate lipofuscin such as the brain and cardiac or skeletal muscles.

Background autofluorescence of biological samples often complicates fluorescence-based imaging techniques, especially in aged human postmitotic tissues. This protocol describes how autofluorescence from these samples can be effectively removed using a commercially available light emitting diode light source to photobleach the sample prior to immunostaining.

Simple élimination de Fluorescence de fond dans les tissus cérébraux humains fixés au formol pour la microscopie en Immunofluorescence

Immunofluorescence is a common method used to visualize subcellular compartments and to determine the localization of specific proteins within a tissue ...

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Biochimie

Combining X-Ray Crystallography with Small Angle X-Ray Scattering to Model Unstructured Regions of Nsa1 from S. Cerevisiae

Determination of the full-length structure of ribosome assembly factor Nsa1 from Saccharomyces cerevisiae (S. cerevisiae) is challenging because of the disordered and protease labile C-terminus of the protein. This manuscript describes the methods to purify recombinant Nsa1 from S. cerevisiae for structural analysis by both X-ray crystallography and SAXS. X-ray crystallography was utilized to solve the structure of the well-ordered N-terminal WD40 domain of Nsa1, and then SAXS was used to resolve the structure of the C-terminus of Nsa1 in solution. Solution scattering data was collected from full-length Nsa1 in solution. The theoretical scattering amplitudes were calculated from the high-resolution crystal structure of the WD40 domain, and then a combination of rigid body and ab initio modeling revealed the C-terminus of Nsa1. Through this hybrid approach the quaternary structure of the entire protein was reconstructed. The methods presented here should be generally applicable for the hybrid structural determination of other proteins composed of a mix of structured and unstructured domains.

Combining X-Ray Crystallography with Small Angle X-Ray Scattering to Model Unstructured Regions of Nsa1 from S. Cerevisiae

This method describes the cloning, expression, and purification of recombinant Nsa1 for structural determination by X-ray crystallography and small-angle X-ray scattering (SAXS), and is applicable for the hybrid structural analysis of other proteins containing both ordered and disordered domains.

Combinant la diffractométrie de rayons x avec la diffusion des rayons x petit Angle pour modéliser des régions non structurées de Nsa1 de S. Cerevisiae

Determination of the full-length structure of ribosome assembly factor Nsa1 from Saccharomyces cerevisiae (S. cerevisiae) is challenging because of the ...

Growing Protein Crystals with Distinct Dimensions Using Automated Crystallization Coupled with In Situ Dynamic Light Scattering

The automated crystallization device is a patented technique1 especially developed for monitoring protein crystallization experiments with the aim to precisely maneuver the nucleation and crystal growth towards desired sizes of protein crystals. The controlled crystallization is based on sample investigation with in situ Dynamic Light Scattering (DLS) while all visual changes in the droplet are monitored online with the help of a microscope coupled to a CCD camera, thus enabling a full investigation of the protein droplet during all stages of crystallization. The use of in situ DLS measurements throughout the entire experiment allows a precise identification of the highly supersaturated protein solution transitioning to a new phase &#8211; the formation of crystal nuclei. By identifying the protein nucleation stage, the crystallization can be optimized from large protein crystals to the production of protein microcrystals. The experimental protocol shows an interactive crystallization approach based on precise automated steps such as precipitant addition, water evaporation for inducing high supersaturation, and sample dilution for slowing induced homogeneous nucleation or reversing phase transitions.

Growing Protein Crystals with Distinct Dimensions Using Automated Crystallization Coupled with In Situ Dynamic Light Scattering

Here we present a protocol for controlled production of protein microcrystals. The process uses an automated device allowing controlled manipulation of several crystallization parameters. The protein crystallization is carried-out by controlled and automated addition of crystallization solutions while monitoring and investigating the radius distribution of particles in the crystallization droplet.

Des cristaux de protéine croissante avec des Dimensions distinctes à l’aide d’automatisé cristallisation couplée avec In Situ diffusion dynamique de la lumière

The automated crystallization device is a patented technique1 especially developed for monitoring protein crystallization experiments with the aim to ...

Characterization of Glycoproteins with the Immunoglobulin Fold by X-Ray Crystallography and Biophysical Techniques

Glycoproteins on the surface of cells play critical roles in cellular function, including signalling, adhesion and transport. On leukocytes, several of these glycoproteins possess immunoglobulin (Ig) folds and are central to immune recognition and regulation. Here, we present a platform for the design, expression and biophysical characterization of the extracellular domain of human B cell receptor CD22. We propose that these approaches are broadly applicable to the characterization of mammalian glycoprotein ectodomains containing Ig domains. Two suspension human embryonic kidney (HEK) cell lines, HEK293F and HEK293S, are used to express glycoproteins harbouring complex and high-mannose glycans, respectively. These recombinant glycoproteins with different glycoforms allow investigating the effect of glycan size and composition on ligand binding. We discuss protocols for studying the kinetics and thermodynamics of glycoprotein binding to biologically relevant ligands and therapeutic antibody candidates. Recombinant glycoproteins produced in HEK293S cells are amenable to crystallization due to glycan homogeneity, reduced flexibility and susceptibility to endoglycosidase H treatment. We present methods for soaking glycoprotein crystals with heavy atoms and small molecules for phase determination and analysis of ligand binding, respectively. The experimental protocols discussed here hold promise for the characterization of mammalian glycoproteins to give insight into their function and investigate the mechanism of action of therapeutics.

We present approaches for the biophysical and structural characterization of glycoproteins with the immunoglobulin fold by biolayer interferometry, isothermal titration calorimetry, and X-ray crystallography.

Caractérisation des glycoprotéines dont le pli d’immunoglobuline par cristallographie aux rayons x et Techniques biophysiques

Glycoproteins on the surface of cells play critical roles in cellular function, including signalling, adhesion and transport. On leukocytes, several of ...

Structural Studies of Macromolecules in Solution using Small Angle X-Ray Scattering

Protein-protein interactions involving proteins with multiple globular domains present technical challenges for determining how such complexes form and how the domains are oriented/positioned. Here, a protocol with the potential for elucidating which specific domains mediate interactions in multicomponent system through ab initio modeling is described. A method for calculating solution structures of macromolecules and their assemblies is provided that involves integrating data from small angle X-ray scattering (SAXS), chromatography, and atomic resolution structures together in a hybrid approach. A specific example is that of the complex of full-length nidogen-1, which assembles extracellular matrix proteins and forms an extended, curved nanostructure. One of its globular domains attaches to laminin &#947;-1, which structures the basement membrane. This provides a basis for determining accurate structures of flexible multidomain protein complexes and is enabled by synchrotron sources coupled with automation robotics and size exclusion chromatography systems. This combination allows rapid analysis in which multiple oligomeric states are separated just prior to SAXS data collection. The analysis yields information on the radius of gyration, particle dimension, molecular shape and interdomain pairing. The protocol for generating 3D models of complexes by fitting high-resolution structures of the component proteins is also given.

Here, we present how Small Angle X-Ray Scattering (SAXS) can be utilized to obtain information on low-resolution envelopes representing the macromolecular structures. When used in conjunction with high-resolution structural techniques such as X-Ray Crystallography and Nuclear Magnetic Resonance, SAXS can provide detailed insights into multidomain proteins and macromolecular complexes in-solution.

Études structurale des macromolécules en Solution à l’aide de petite diffusion des rayons x Angle

Protein-protein interactions involving proteins with multiple globular domains present technical challenges for determining how such complexes form and ...

A Plasma Sample Preparation for Mass Spectrometry using an Automated Workstation

Sample preparation for mass spectrometry analysis in proteomics requires enzymatic cleavage of proteins into a peptide mixture. This process involves numerous incubation and liquid transfer steps in order to achieve denaturation, reduction, alkylation, and cleavage. Adapting this workflow onto an automated workstation can increase efficiency and reduce coefficients of variance, thereby providing more reliable data for statistical comparisons between sample types. We previously described an automated proteomic sample preparation workflow1. Here, we report the development of a more efficient and better controlled workflow with the following advantages: 1) The number of liquid transfer steps is reduced from nine to six by combining reagents; 2) Pipetting time is reduced by selective tip pipetting using a 96-position pipetting head with multiple channels; 3) Potential throughput is increased by the availability of up to 45 deck positions; 4) Complete enclosure of the system provides improved temperature and environmental control and reduces the potential for contamination of samples or reagents; and 5) The addition of stable isotope labeled peptides, as well as &#946;-galactosidase protein, to each sample makes monitoring and quality control possible throughout the entire process. These hardware and process improvements provide good reproducibility and improve intra-assay and inter-assay precision (CV of less than 20%) for LC-MS based protein and peptide quantification. The entire workflow for digesting 96 samples in a 96-well plate can be completed in approximately 5 hours.

Here, we present an automated plasma protein digestion method for mass spectrometry-based quantitative proteomic analysis. In this protocol, the liquid transferring and incubation steps for protein denaturation, reduction, alkylation, and trypsin digestion reactions are streamlined and automated. It takes approximately five hours to prepare a 96-well plate with desired precision.

Préparation d’un échantillon de plasma pour la spectrométrie de masse à l’aide d’un poste de travail automatisé

Sample preparation for mass spectrometry analysis in proteomics requires enzymatic cleavage of proteins into a peptide mixture. This process involves ...

Cell Culture on Silicon Nitride Membranes and Cryopreparation for Synchrotron X-ray Fluorescence Nano-analysis

Very little is known about the distribution of metal ions at the subcellular level. However, those chemical elements have essential regulatory functions and their disturbed homeostasis is involved in various diseases. State-of-the-art synchrotron X-ray fluorescence nanoprobes provide the required sensitivity and spatial resolution to elucidate the two-dimensional (2D) and three-dimensional (3D) distribution and concentration of metals inside entire cells at the organelle level. This opens new exciting scientific fields of investigation on the role of metals in the physiopathology of the cell. The cellular preparation is a key and often complex procedure, particularly for basic analysis. Although X-ray fluorescence techniques are now widespread and various preparation methods have been used, very few studies have investigated the preservation of the elemental content of cells at best, and no stepwise detailed protocol for the cryopreparation of adherent cells for X-ray fluorescence nanoprobes has been released so far. This is a description of a protocol that provides the stepwise cellular preparation for fast cryofixation to enable synchrotron X-ray fluorescence nano-analysis of cells in a frozen hydrated state when a cryogenic environment and transfer is available. In case nano-analysis has to be performed at room temperature, an additional procedure for freeze-drying the cryofixed adherent cellular preparation is provided. The proposed protocols have been successfully used in previous works, most recently in studying the 2D and 3D intracellular distribution of an organometallic compound in breast cancer cells.

Presented here is a protocol for cell culture on silicon nitride membranes and plunge-freezing prior to X-ray fluorescence imaging with a synchrotron cryogenic X-ray nanoprobe. When only room temperature nano-analysis is provided, the frozen samples can be further freeze-dried. These are critical steps to obtain information on the intracellular elemental composition.

Cell Culture on Silicon Nitride Membranes and Cryopreparation for Synchrotron X-ray Fluorescence Nano-analyse

Very little is known about the distribution of metal ions at the subcellular level. However, those chemical elements have essential regulatory functions ...

X-Ray Crystallography to Study the Oligomeric State Transition of the Thermotoga maritima M42 Aminopeptidase TmPep1050

The M42 aminopeptidases form functionally active complexes made of 12 subunits. Their assembly process appears to be regulated by their metal ion cofactors triggering a dimer-dodecamer transition. Upon metal ion binding, several structural modifications occur in the active site and at the interaction interface, shaping dimers to promote the self-assembly. To observe such modifications, stable oligomers must be isolated prior to structural study. Reported here is a method that allows the purification of stable dodecamers and dimers of TmPep1050, an M42 aminopeptidase of T. maritima, and their structure determination by X-ray crystallography. Dimers were prepared from dodecamers by removing metal ions with a chelating agent. Without their&#160;cofactor, dodecamers became less stable and were fully dissociated upon heating. The oligomeric structures were solved by the straightforward molecular replacement approach. To illustrate the methodology, the structure of a TmPep1050 variant, totally impaired in metal ion binding, is presented showing no further breakdown of dimers to monomers.

X-Ray Crystallography to Study the Oligomeric State Transition of the Thermotoga maritima M42 Aminopeptidase TmPep1050

This protocol has been developed to study the dimer-dodecamer transition of TmPep1050, an M42 aminopeptidase, at the structural level. It is a straightforward pipeline starting from protein purification to X-ray data processing. Crystallogenesis, data set indexation, and molecular replacement have been emphasized through a case of study, TmPep1050H60A H307A variant.

Cristallographie aux rayons X pour étudier la transition oligomérique de l’État de la Thermotoga maritima M42 Aminopeptidase TmPep1050

The M42 aminopeptidases form functionally active complexes made of 12 subunits. Their assembly process appears to be regulated by their metal ion ...

Plant Sample Preparation for Nucleoside/Nucleotide Content Measurement with An HPLC-MS/MS

Nucleosides/nucleotides are building blocks of nucleic acids, parts of cosubstrates and coenzymes, cell signaling molecules, and energy carriers, which are involved in many cell activities. Here, we describe a rapid and reliable method for the absolute qualification of nucleoside/nucleotide contents in plants. Briefly, 100 mg of homogenized plant material was extracted with 1 mL of extraction buffer (methanol, acetonitrile, and water at a ratio of 2:2:1). Later, the sample was concentrated five times in a freeze dryer and then injected into an HPLC-MS/MS. Nucleotides were separated on a porous graphitic carbon (PGC) column and nucleosides were separated on a C18 column. The mass transitions of each nucleoside and nucleotide were monitored by mass spectrometry. The contents of the nucleosides and nucleotides were quantified against their external standards (ESTDs). Using this method, therefore, researchers can easily quantify nucleosides/nucleotides in different plants.

A precise and reproducible method for in vivo nucleosides/nucleotides quantification in plants is described here. This method employs an HPLC-MS/MS.

Préparation d’échantillons de plantes pour la mesure de la teneur en nucléosides/nucléotides avec une CLHP-MS/MS

Nucleosides/nucleotides are building blocks of nucleic acids, parts of cosubstrates and coenzymes, cell signaling molecules, and energy carriers, which ...

Crystallization and Structural Determination of an Enzyme:Substrate Complex by Serial Crystallography in a Versatile Microfluidic Chip

The preparation of well diffracting crystals and their handling before their X-ray analysis are two critical steps of biocrystallographic studies. We describe a versatile microfluidic chip that enables the production of crystals by the efficient method of counter-diffusion. The convection-free environment provided by the microfluidic channels is ideal for crystal growth and useful to diffuse a substrate into the active site of the crystalline enzyme. Here we applied this approach to the CCA-adding enzyme of the psychrophilic bacterium Planococcus halocryophilus in the presented example. After crystallization and substrate diffusion/soaking, the crystal structure of the enzyme:substrate complex was determined at room temperature by serial crystallography and the analysis of multiple crystals directly inside the chip. The whole procedure preserves the genuine diffraction properties of the samples because it requires no crystal handling.

A versatile microfluidic device is described that enables the crystallization of an enzyme using the counter-diffusion method, the introduction of a substrate in the crystals by soaking, and the 3D structure determination of the enzyme:substrate complex by a serial analysis of crystals inside the chip at room temperature.

Cristallisation et détermination structurale d’une enzyme : complexe de substrat par cristallographie sérielle dans une puce microfluidique polyvalente

The preparation of well diffracting crystals and their handling before their X-ray analysis are two critical steps of biocrystallographic studies. We ...