- 1. Introduction
- 2. Design and use of 3D-printed IMISX sample holders
- 3. Post-treatment capabilities of the 3D-printed IMISX sample holders
- 4. Data collection with the 3D-printed IMISX sample holders
- 5. Discussion and remarks
- 6. Related literature
- 7. 3D-printer files
- Supporting information
- References
- 1. Introduction
- 2. Design and use of 3D-printed IMISX sample holders
- 3. Post-treatment capabilities of the 3D-printed IMISX sample holders
- 4. Data collection with the 3D-printed IMISX sample holders
- 5. Discussion and remarks
- 6. Related literature
- 7. 3D-printer files
- Supporting information
- References
laboratory notes
3D-printed holders for in meso in situ fixed-target serial X-ray crystallography
aPaul Scherrer Institute, Forschungsstrasse 111, Villigen-PSI, 5232, Switzerland, and bMembrane Structural and Functional Biology Group, Trinity Biomedical Sciences Institute, Trinity College, Dublin 2, D02 R590, Ireland
*Correspondence e-mail: chia-ying.huang@psi.ch
The in meso in situ serial X-ray crystallography method was developed to ease the handling of small fragile crystals of membrane proteins and for rapid data collection on hundreds of microcrystals directly in the growth medium without the need for crystal harvesting. To facilitate mounting of these in situ samples on a goniometer at cryogenic or at room temperatures, two new 3D-printed holders have been developed. They provide for cubic and sponge phase sample stability in the X-ray beam and are compatible with sample-changing robots. The holders can accommodate a variety of window material types, as well as bespoke samples for diffraction screening and data collection at conventional macromolecular crystallography beamlines. They can be used for convenient post-crystallization treatments such as ligand and heavy-atom soaking. The design, assembly and application of the holders for in situ serial crystallography are described. Files for making the holders using a 3D printer are included as supporting information.
Keywords: 3D-printed holders; IMISX; in meso in situ serial X-ray crystallography; fixed targets; post-crystallization treatments.
1. Introduction
In meso or lipid cubic phase crystallization has played an important role in X-ray of membrane proteins, especially G-protein coupled receptors and the complexes they form (Cherezov et al., 2007; Jaakola et al., 2008; Chien et al., 2010; Wu et al., 2010; Caffrey, 2015). The cubic phase has also found application as a native-like medium in which to port crystals across beams for time-resolved serial crystallography at synchrotron (Nogly et al., 2015; Weinert et al., 2017) and free-electron laser X-ray sources (Weierstall et al., 2014; White et al., 2016; Nogly et al., 2018; Cheng, 2020). The recently developed in situ in meso serial X-ray crystallography (IMISX) method uses perforated double-stick tape to create wells for crystallization and supporting sachets (IMISX wells) in which to deliver the crystal-laden to the X-ray beam without the need for direct crystal harvesting (Huang et al., 2015, 2016, 2018; El Ghachi et al., 2018; Apel et al., 2019; Cheng et al., 2019). The original IMISX method involved securing a slightly curved thin-film sachet to a pin on a goniometer (Fig. 1) (Huang et al., 2016). Curvature was imposed to provide mechanical stability to the sachet in the cryostream. A Y-shaped support was introduced subsequently to facilitate data collection over a large flat – as opposed to a curved – sample area. However, this holder proved to be time consuming to assemble and not particularly practical to use (Huang et al., 2018). Separately, self-closing clips were developed to improve the efficiency of in situ sample preparation. These included the DiffraX metal sample holder (Axford et al., 2016) and a 3D-printed device (Broecker et al., 2016, 2018). Here we introduce two new 3D-printed sample holders. Compared with previous clips, they are extremely easy to assemble – from two identical pieces. They provide increased mechanical stability, they limit ice formation when collecting diffraction data in a cryogenic stream and they facilitate post-crystallization treatments. The first holder, h1, is suited to samples in which crystals have been grown and remain in the viscous The second, h2, was designed for samples in which the more fluid variant of the cubic phase, the sponge phase (Cherezov et al., 2006; Caffrey, 2015), has formed. Both holders can be used for room-temperature (RT, 293 K) data collection and are compatible with sample-changing robots. They provide for a wide scanning area and are suitable for post-crystallization treatments such as ligand and heavy-atom soaking (Li et al., 2015; Rucktooa et al., 2018; Huang et al., 2018). The holders can be used with a host of in situ window materials such as cyclic olefin polymer (COP) (Axford et al., 2016; Apel et al., 2019), cyclic olefin (COC) (Huang et al., 2015, 2016; El Ghachi et al., 2018), biaxially oriented polyethylene terephthalate (Mylar) (Broecker et al., 2016) and silicon nitride (Cherezov & Caffrey, 2007; Murray et al., 2015; Roedig et al., 2015; Owen et al., 2017). Furthermore, the holders are 3D printed and reusable.
2. Design and use of 3D-printed IMISX sample holders
The IMISX sample holders are made of poly(methyl methacrylate) (PMMA), also known as acrylic or plexiglass, a plastic material with exceptional strength and rigidity [Figs. 2(a) and 2(b)]. PMMA proved to be particularly suitable for the faithful printing of fine details (on the scale of 0.1 mm) and for providing a surface with a uniformly smooth finish. Fabrication was done using a 3D printer (ProJet MJP 2500 Plus, 3D Systems, USA). Both holder types have three functional parts: a base, an arm and a sachet clamp (Fig. 2). In the first holder type, h1, the clamp is rectangular in outline and has a four-sided frame [Fig. 2(a)]. The second type, h2, has a semi-circular clamp with an open end and has a larger sample area than h1 [Fig. 2(b)]. Both holders are built on the principle of reverse or self-closing tweezers. They are assembled from identical halves that perfectly align together via mating male (pin) and female (hole/receptacle) connectors at the base of the holder [Figs. 2(c)–2(e), yellow and blue arrows]. The coupled pair is inserted into a commercial magnetic base (CryoCaps from Molecular Dimension, UK) and secured in place with glue (instant glue, ethyl 2-cyanoacrylate, Cementit, Switzerland) [Figs. 2(f)–2(g)]. The holder can be opened and closed for loading and unloading simply by pressing on and releasing the criss-crossed arms of the device using a finger and thumb [Fig. 2(h)] or tweezers [Fig. 2(i)] (Axford et al., 2016; Broecker et al., 2018).
The sachet clamp in h1 consists of a 4 × 2 × 1.4 mm apron, two 1 × 6 × 0.3 mm jambs and two 1 × 1 × 0.15 mm heads [Fig. 2(a)]. These serve to pinch and, in so doing, to hold the sachet firmly in place, leaving a 0.3 mm gap for post-crystallization treatments [Fig. 3(e)]. The mesophase-laden sachet is prepared by cutting it out of the IMISX plate with outside margins of approximately 2 mm. An online open-access movie is available to show how this is done (Huang et al., 2016). The freed sachet is then secured in the clamp by adjusting its jaws with the criss-crossed arms by hand or with tweezers [Figs. 3(a) and 2(i)]. To facilitate centering once the sample is mounted on the goniometer, the bolus of in the sachet is centered in the window of the clamp [Fig. 3(c)]. The clamp in h2 is similar to that in h1 with the exception that it incorporates a semi-circular frame with an outside diameter of 4 mm [Fig. 2(b)]. Positioning a sachet in h2 is done as described for the h1 holder [Figs. 3(b), 3(d) and 3(f)].
The oscillation range that is possible with these holders is ±30°. It is important to pre-align the pin-mounted holders before placing them on the goniometer so that they end up with the plane of the sachet perpendicular to the X-ray beam and, for cryogenic data collection, with an optimal orientation with respect to the cryostream to reduce frosting. The holders can be frozen to liquid-nitrogen temperatures, thawed and reused.
3. Post-treatment capabilities of the 3D-printed IMISX sample holders
The IMISX sachets greatly facilitate crystal soaking with ligands and heavy atoms (Huang et al., 2018). The samples are protected at all times during the process by controlling local temperature and humidity. To perform a soaking exercise, the sachet is first opened by cutting it with a pair of scissors along one side of the rectangular h1 clamp [Fig. 4(a)] or across the top of the round sachet in the h2 holders [Fig. 4(b)]. The standoffs in the clamp of the h1 holder provide a 0.3 mm gap between the two frames [Fig. 3(e)] for dispensing soaking and wash solutions [Fig. 4(c)]. In the h2 holder, solutions are easily added to and removed from the exposed cut end of the sachet [Fig. 4(d)]. Prior to data collection at RT or storage in liquid nitrogen, the samples can be kept during the soaking interval (typically less than 1 h) at 293 K in a closed box with a wet tissue to minimize dehydration.
4. Data collection with the 3D-printed IMISX sample holders
To assess the quality of data that can be collected with both h1 and h2 holders at ambient and cryogenic temperatures, we used crystals of native lysozyme (Lyso native RT), bromine-derivatized lysozyme (LysoBr cryo and LysoBr RT) and the membrane protein PepTSt (PepTSt cryo) (Supplementary Table S1). With lysozyme, an IMISX sachet with in meso-grown crystals (10 × 20 × 30 µm) was removed from an IMISX plate, mounted on an h1 holder and soaked with sodium bromide (see supporting information) as described previously (Fig. 4). The sample was mounted using the TELL sample changer (Martiel et al., 2020) and measured at 100 K using a wavelength of 0.91969 Å at the Swiss Light Source (SLS) beamline X10SA-PXII with a beam of 20 × 10 µm and values of 5 × 1011 photons s−1. The data sets collected from 12 crystals over 20° wedges for each crystal were merged and used for phasing by Br single-wavelength anomalous diffraction with SHELXC/D (Sheldrick, 2010) and Crank2 (Skubák & Pannu, 2013) [Supplementary Table S1 and Supplementary Figs. 1(a) and 1(c)]. The structure was refined to Rwork/Rfree values of 0.19/0.21 at a resolution of 1.80 Å.
In the case of PepTSt cryo, crystals grow in the sponge phase. Accordingly, measurements were made with an h2 holder. The crystals, with maximum dimensions of 10 × 15 × 15 µm, were used for data collection at a wavelength of 1 Å on SLS beamline X06SA-PXI at 100 K with a beam of 20 × 10 µm and values of 3.7 × 1011 photons s−1. Twenty-nine data sets over 10° wedges for each crystal were combined to obtain complete data to a resolution of 2.53 Å (Supplementary Table S1). The structure was solved by using PDB entry 5d58 (Huang et al., 2016) as the model and refined to Rwork/Rfree values of 0.23/0.26.
The h1 holder has also been tested with data collection at RT using the same lysozyme native crystals (Lyso native RT) and LysoBr crystals (LysoBr RT) described above at a wavelength of 0.91881 Å on SLS beamline X06SA-PXI at 293 K with a beam of 20 × 10 µm and 10 photons s−1. The Br anomalous signal from 200 LysoBr data sets at RT over 10° wedges for each crystal was combined with high-resolution data from 15 Lyso native RT crystals over 10° wedges for each crystal for phasing with single with using SHELXC/D and Crank2 [Supplementary Table S1 and Supplementary Figs. 1(b) and 1(d)]. The structure was refined to Rwork/Rfree values of 0.18/0.21 using Lyso native RT at a resolution of 1.8 Å.
values of 1.4 × 105. Discussion and remarks
The development of serial crystallographic data collection methods is a perpetual pursuit at synchrotron and XFEL facilities worldwide. The sample holders described here were designed to meet the need for convenient in meso sample preparation and high-throughput in situ crystallographic data collection. The new holders are easy to assemble and load with sachets cut from IMISX plates and lend themselves to convenient ligand and heavy-atom soaking and screening of crystals in situ in a protective environment. The holders can be used to store samples under cryogenic conditions for subsequent high-throughput screening with automated sample changers. High-quality data can be obtained at 100 K courtesy of the mechanical stability of the IMISX sachet in the cryogenic stream when mounted in the new 3D-printed holders. In addition, the low profile of the holders has the effect of minimally disturbing the cryogenic gas stream flow, thereby reducing ice formation on the sample. The holders can also be used for data collection at ambient temperatures. They are compatible with a variety of window material types including COC, COP, Mylar and silicon nitride and can be used for serial crystallographic measurements at home, synchrotron and free-electron laser X-ray sources.
The IMISX method was developed to enable the handling of fragile crystals in a viscous
and for highly efficient, close-to-automatic crystallographic data collection at ambient and cryogenic temperatures. The new holders introduced here make sample preparation, handing and post-crystallization treatment (ligand and heavy-atom screening) extremely easy. With access to a 3D printer, the new holders can be generated quickly and inexpensively using the open-access files associated with this paper. Furthermore, refinements can be made to suit specific applications by simply modifying the files and/or by using different fabricating materials. We believe these holders will prove to be generally useful and will contribute to expediting the of proteins and complexes that are scientifically and medically important.6. Related literature
The following additional literature is cited in the supporting information: Basu et al. (2019), Kabsch, W. (2010a,b), Lyons et al. (2014), McCoy et al. (2007) and Pape & Schneider (2004).
7. 3D-printer files
Files for the sample holders are available in .stl format as supporting information.
Supporting information
3D-printer file: h1 holder. DOI: https://doi.org/10.1107/S1600576720002897/gj5239sup1.stl
3D-printer file: h2 holder. DOI: https://doi.org/10.1107/S1600576720002897/gj5239sup2.stl
Supplementary Information. DOI: https://doi.org/10.1107/S1600576720002897/gj5239sup3.pdf
Acknowledgements
We thank scientists/engineers of the Reprography of Engineering and Coordination Department at Paul Scherrer Institute for advice regarding the design and fabrication of the 3D-printed holders introduced here. The assistance and support of beamline scientists at the Swiss Light Source beamlines X06SA-PXI and X10SA-PXII are acknowledged.
Funding information
CYH is partially supported by the European Union's Horizon 2020 research and innovation program under the Marie-Skłodowska-Curie grant agreement No. 701647. The work was funded in part by Science Foundation Ireland (16/IA/4435).
References
Apel, A. K., Cheng, R. K. Y., Tautermann, C. S., Brauchle, M., Huang, C. Y., Pautsch, A., Hennig, M., Nar, H. & Schnapp, G. (2019). Structure, 27, 427–438.e5. Web of Science CrossRef CAS PubMed Google Scholar
Axford, D., Aller, P., Sanchez-Weatherby, J. & Sandy, J. (2016). Acta Cryst. F72, 313–319. Web of Science CrossRef IUCr Journals Google Scholar
Basu, S., Kaminski, J. W., Panepucci, E., Huang, C.-Y., Warshamanage, R., Wang, M. & Wojdyla, J. A. (2019). J. Synchrotron Rad. 26, 244–252. Web of Science CrossRef CAS IUCr Journals Google Scholar
Broecker, J., Klingel, V., Ou, W. L., Balo, A. R., Kissick, D. J., Ogata, C. M., Kuo, A. & Ernst, O. P. (2016). Cryst. Growth Des. 16, 6318–6326. Web of Science CrossRef CAS PubMed Google Scholar
Broecker, J., Morizumi, T., Ou, W. L., Klingel, V., Kuo, A., Kissick, D. J., Ishchenko, A., Lee, M. Y., Xu, S., Makarov, O., Cherezov, V., Ogata, C. M. & Ernst, O. P. (2018). Nat. Protoc. 13, 260–292. Web of Science CrossRef CAS PubMed Google Scholar
Caffrey, M. (2015). Acta Cryst. F71, 3–18. Web of Science CrossRef IUCr Journals Google Scholar
Cheng, R. (2020). Crystals, 10, 215. Web of Science CrossRef Google Scholar
Cheng, R., Huang, C. Y., Hennig, M., Nar, H. & Schnapp, G. (2019). FEBS J. 287, 866–873. Web of Science CrossRef PubMed Google Scholar
Cherezov, V. & Caffrey, M. (2007). Faraday Discuss. 136, 195–212; discussion 213–129. Google Scholar
Cherezov, V., Clogston, J., Papiz, M. Z. & Caffrey, M. (2006). J. Mol. Biol. 357, 1605–1618. Web of Science CrossRef PubMed CAS Google Scholar
Cherezov, V., Rosenbaum, D. M., Hanson, M. A., Rasmussen, S. G., Thian, F. S., Kobilka, T. S., Choi, H. J., Kuhn, P., Weis, W. I., Kobilka, B. K. & Stevens, R. C. (2007). Science, 318, 1258–1265. Web of Science CrossRef PubMed CAS Google Scholar
Chien, E. Y., Liu, W., Zhao, Q., Katritch, V., Won Han, G., Hanson, M. A., Shi, L., Newman, A. H., Javitch, J. A., Cherezov, V. & Stevens, R. C. (2010). Science, 330, 1091–1095. Web of Science CrossRef CAS PubMed Google Scholar
El Ghachi, M., Howe, N., Huang, C. Y., Olieric, V., Warshamanage, R., Touzé, T., Weichert, D., Stansfeld, P. J., Wang, M., Kerff, F. & Caffrey, M. (2018). Nat. Commun. 9, 1078. Web of Science CrossRef PubMed Google Scholar
Huang, C. Y., Olieric, V., Howe, N., Warshamanage, R., Weinert, T., Panepucci, E., Vogeley, L., Basu, S., Diederichs, K., Caffrey, M. & Wang, M. (2018). Commun. Biol. 1, 124. Web of Science CrossRef PubMed Google Scholar
Huang, C.-Y., Olieric, V., Ma, P., Howe, N., Vogeley, L., Liu, X., Warshamanage, R., Weinert, T., Panepucci, E., Kobilka, B., Diederichs, K., Wang, M. & Caffrey, M. (2016). Acta Cryst. D72, 93–112. Web of Science CrossRef IUCr Journals Google Scholar
Huang, C.-Y., Olieric, V., Ma, P., Panepucci, E., Diederichs, K., Wang, M. & Caffrey, M. (2015). Acta Cryst. D71, 1238–1256. Web of Science CrossRef IUCr Journals Google Scholar
Jaakola, V. P., Griffith, M. T., Hanson, M. A., Cherezov, V., Chien, E. Y., Lane, J. R., Ijzerman, A. P. & Stevens, R. C. (2008). Science, 322, 1211–1217. Web of Science CrossRef PubMed CAS Google Scholar
Kabsch, W. (2010a). Acta Cryst. D66, 125–132. Web of Science CrossRef CAS IUCr Journals Google Scholar
Kabsch, W. (2010b). Acta Cryst. D66, 133–144. Web of Science CrossRef CAS IUCr Journals Google Scholar
Li, D., Pye, V. E. & Caffrey, M. (2015). Acta Cryst. D71, 104–122. Web of Science CrossRef IUCr Journals Google Scholar
Lyons, J. A., Parker, J. L., Solcan, N., Brinth, A., Li, D., Shah, S. T., Caffrey, M. & Newstead, S. (2014). EMBO Rep. 15, 886–893. Web of Science CrossRef CAS PubMed Google Scholar
Martiel, I., Buntschu, D., Meier, N., Gobbo, A., Panepucci, E., Schneider, R., Heimgartner, P., Müller, D., Bühlmann, K., Birri, M., Kaminski, J. W., Leuenberger, J., Oliéric, V., Glettig, W. & Wang, M. (2020). J. Synchrotron Rad. 27, 860–863. CrossRef CAS IUCr Journals Google Scholar
McCoy, A. J., Grosse-Kunstleve, R. W., Adams, P. D., Winn, M. D., Storoni, L. C. & Read, R. J. (2007). J. Appl. Cryst. 40, 658–674. Web of Science CrossRef CAS IUCr Journals Google Scholar
Murray, T. D., Lyubimov, A. Y., Ogata, C. M., Vo, H., Uervirojnangkoorn, M., Brunger, A. T. & Berger, J. M. (2015). Acta Cryst. D71, 1987–1997. Web of Science CrossRef IUCr Journals Google Scholar
Nogly, P., James, D., Wang, D., White, T. A., Zatsepin, N., Shilova, A., Nelson, G., Liu, H., Johansson, L., Heymann, M., Jaeger, K., Metz, M., Wickstrand, C., Wu, W., Båth, P., Berntsen, P., Oberthuer, D., Panneels, V., Cherezov, V., Chapman, H., Schertler, G., Neutze, R., Spence, J., Moraes, I., Burghammer, M., Standfuss, J. & Weierstall, U. (2015). IUCrJ, 2, 168–176. Web of Science CrossRef CAS PubMed IUCr Journals Google Scholar
Nogly, P., Weinert, T., James, D., Carbajo, S., Ozerov, D., Furrer, A., Gashi, D., Borin, V., Skopintsev, P., Jaeger, K., Nass, K., Bath, P., Bosman, R., Koglin, J., Seaberg, M., Lane, T., Kekilli, D., Brunle, S., Tanaka, T., Wu, W., Milne, C., White, T., Barty, A., Weierstall, U., Panneels, V., Nango, E., Iwata, S., Hunter, M., Schapiro, I., Schertler, G., Neutze, R. & Standfuss, J. (2018). Science, 361, 6398. Google Scholar
Owen, R. L., Axford, D., Sherrell, D. A., Kuo, A., Ernst, O. P., Schulz, E. C., Miller, R. J. D. & Mueller-Werkmeister, H. M. (2017). Acta Cryst. D73, 373–378. Web of Science CrossRef IUCr Journals Google Scholar
Pape, T. & Schneider, T. R. (2004). J. Appl. Cryst. 37, 843–844. Web of Science CrossRef CAS IUCr Journals Google Scholar
Roedig, P., Vartiainen, I., Duman, R., Panneerselvam, S., Stübe, N., Lorbeer, O., Warmer, M., Sutton, G., Stuart, D. I., Weckert, E., David, C., Wagner, A. & Meents, A. (2015). Sci. Rep. 5, 10451. Web of Science CrossRef PubMed Google Scholar
Rucktooa, P., Cheng, R. K. Y., Segala, E., Geng, T., Errey, J. C., Brown, G. A., Cooke, R. M., Marshall, F. H. & Doré, A. S. (2018). Sci. Rep. 8, 41. Web of Science CrossRef PubMed Google Scholar
Sheldrick, G. M. (2010). Acta Cryst. D66, 479–485. Web of Science CrossRef CAS IUCr Journals Google Scholar
Skubák, P. & Pannu, N. S. (2013). Nat. Commun. 4, 2777. Web of Science PubMed Google Scholar
Weierstall, U., James, D., Wang, C., White, T. A., Wang, D., Liu, W., Spence, J. C., Bruce Doak, R., Nelson, G., Fromme, P., Fromme, R., Grotjohann, I., Kupitz, C., Zatsepin, N. A., Liu, H., Basu, S., Wacker, D., Won Han, G., Katritch, V., Boutet, S., Messerschmidt, M., Williams, G. J., Koglin, J. E., Marvin Seibert, M., Klinker, M., Gati, C., Shoeman, R. L., Barty, A., Chapman, H. N., Kirian, R. A., Beyerlein, K. R., Stevens, R. C., Li, D., Shah, S. T., Howe, N., Caffrey, M. & Cherezov, V. (2014). Nat. Commun. 5, 3309. Web of Science CrossRef PubMed Google Scholar
Weinert, T., Olieric, N., Cheng, R., Brünle, S., James, D., Ozerov, D., Gashi, D., Vera, L., Marsh, M., Jaeger, K., Dworkowski, F., Panepucci, E., Basu, S., Skopintsev, P., Doré, A. S., Geng, T., Cooke, R. M., Liang, M., Prota, A. E., Panneels, V., Nogly, P., Ermler, U., Schertler, G., Hennig, M., Steinmetz, M. O., Wang, M. & Standfuss, J. (2017). Nat. Commun. 8, 542. Web of Science CrossRef PubMed Google Scholar
White, T. A., Barty, A., Liu, W., Ishchenko, A., Zhang, H., Gati, C., Zatsepin, N. A., Basu, S., Oberthur, D., Metz, M., Beyerlein, K. R., Yoon, C. H., Yefanov, O. M., James, D., Wang, D., Messerschmidt, M., Koglin, J. E., Boutet, S., Weierstall, U. & Cherezov, V. (2016). Sci. Data, 3, 160057. Web of Science CrossRef PubMed Google Scholar
Wu, B., Chien, E. Y., Mol, C. D., Fenalti, G., Liu, W., Katritch, V., Abagyan, R., Brooun, A., Wells, P., Bi, F. C., Hamel, D. J., Kuhn, P., Handel, T. M., Cherezov, V. & Stevens, R. C. (2010). Science, 330, 1066–1071. Web of Science CrossRef CAS PubMed Google Scholar
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