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High throughput screening using acoustic droplet ejection to combine protein crystals and chemical libraries on crystallization plates at high density
We describe a high throughput method for screening up to 1728 distinct chemicals with protein crystals on a single microplate. Acoustic droplet ejection (ADE) was used to co-position 2.5nL of protein, precipitant, and chemicals on a MiTeGen in situ-1 crystallization plate™ for screening by co-crysta...
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Published in: | Journal of structural biology 2015-07, Vol.191 (1), p.49-58 |
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container_title | Journal of structural biology |
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creator | Teplitsky, Ella Joshi, Karan Ericson, Daniel L. Scalia, Alexander Mullen, Jeffrey D. Sweet, Robert M. Soares, Alexei S. |
description | We describe a high throughput method for screening up to 1728 distinct chemicals with protein crystals on a single microplate. Acoustic droplet ejection (ADE) was used to co-position 2.5nL of protein, precipitant, and chemicals on a MiTeGen in situ-1 crystallization plate™ for screening by co-crystallization or soaking. ADE-transferred droplets follow a precise trajectory which allows all components to be transferred through small apertures in the microplate lid. The apertures were large enough for 2.5nL droplets to pass through them, but small enough so that they did not disrupt the internal environment created by the mother liquor. Using this system, thermolysin and trypsin crystals were efficiently screened for binding to a heavy-metal mini-library. Fluorescence and X-ray diffraction were used to confirm that each chemical in the heavy-metal library was correctly paired with the intended protein crystal. A fragment mini-library was screened to observe two known lysozyme ligands using both co-crystallization and soaking. A similar approach was used to identify multiple, novel thaumatin binding sites for ascorbic acid. This technology pushes towards a faster, automated, and more flexible strategy for high throughput screening of chemical libraries (such as fragment libraries) using as little as 2.5nL of each component. |
doi_str_mv | 10.1016/j.jsb.2015.05.006 |
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Acoustic droplet ejection (ADE) was used to co-position 2.5nL of protein, precipitant, and chemicals on a MiTeGen in situ-1 crystallization plate™ for screening by co-crystallization or soaking. ADE-transferred droplets follow a precise trajectory which allows all components to be transferred through small apertures in the microplate lid. The apertures were large enough for 2.5nL droplets to pass through them, but small enough so that they did not disrupt the internal environment created by the mother liquor. Using this system, thermolysin and trypsin crystals were efficiently screened for binding to a heavy-metal mini-library. Fluorescence and X-ray diffraction were used to confirm that each chemical in the heavy-metal library was correctly paired with the intended protein crystal. A fragment mini-library was screened to observe two known lysozyme ligands using both co-crystallization and soaking. A similar approach was used to identify multiple, novel thaumatin binding sites for ascorbic acid. This technology pushes towards a faster, automated, and more flexible strategy for high throughput screening of chemical libraries (such as fragment libraries) using as little as 2.5nL of each component.</description><identifier>ISSN: 1047-8477</identifier><identifier>EISSN: 1095-8657</identifier><identifier>DOI: 10.1016/j.jsb.2015.05.006</identifier><identifier>PMID: 26027487</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Acoustic droplet ejection ; Chemical biology ; Crystallization ; Crystallography ; Crystallography, X-Ray ; Drug Discovery ; Fragment screening ; High throughput screening ; In situ X-ray data collection ; MATERIALS SCIENCE ; Proteins - chemistry ; Small Molecule Libraries ; Synchrotron radiation</subject><ispartof>Journal of structural biology, 2015-07, Vol.191 (1), p.49-58</ispartof><rights>2015 The Authors</rights><rights>Copyright © 2015 The Authors. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c493t-135878e101849f23329c89327c5f65446844deea1c023eb047a55e762a325f303</citedby><cites>FETCH-LOGICAL-c493t-135878e101849f23329c89327c5f65446844deea1c023eb047a55e762a325f303</cites><orcidid>0000-0003-2822-771X ; 000000032822771X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26027487$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/1250356$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Teplitsky, Ella</creatorcontrib><creatorcontrib>Joshi, Karan</creatorcontrib><creatorcontrib>Ericson, Daniel L.</creatorcontrib><creatorcontrib>Scalia, Alexander</creatorcontrib><creatorcontrib>Mullen, Jeffrey D.</creatorcontrib><creatorcontrib>Sweet, Robert M.</creatorcontrib><creatorcontrib>Soares, Alexei S.</creatorcontrib><creatorcontrib>Brookhaven National Laboratory (BNL), Upton, NY (United States)</creatorcontrib><title>High throughput screening using acoustic droplet ejection to combine protein crystals and chemical libraries on crystallization plates at high density</title><title>Journal of structural biology</title><addtitle>J Struct Biol</addtitle><description>We describe a high throughput method for screening up to 1728 distinct chemicals with protein crystals on a single microplate. Acoustic droplet ejection (ADE) was used to co-position 2.5nL of protein, precipitant, and chemicals on a MiTeGen in situ-1 crystallization plate™ for screening by co-crystallization or soaking. ADE-transferred droplets follow a precise trajectory which allows all components to be transferred through small apertures in the microplate lid. The apertures were large enough for 2.5nL droplets to pass through them, but small enough so that they did not disrupt the internal environment created by the mother liquor. Using this system, thermolysin and trypsin crystals were efficiently screened for binding to a heavy-metal mini-library. Fluorescence and X-ray diffraction were used to confirm that each chemical in the heavy-metal library was correctly paired with the intended protein crystal. A fragment mini-library was screened to observe two known lysozyme ligands using both co-crystallization and soaking. A similar approach was used to identify multiple, novel thaumatin binding sites for ascorbic acid. This technology pushes towards a faster, automated, and more flexible strategy for high throughput screening of chemical libraries (such as fragment libraries) using as little as 2.5nL of each component.</description><subject>Acoustic droplet ejection</subject><subject>Chemical biology</subject><subject>Crystallization</subject><subject>Crystallography</subject><subject>Crystallography, X-Ray</subject><subject>Drug Discovery</subject><subject>Fragment screening</subject><subject>High throughput screening</subject><subject>In situ X-ray data collection</subject><subject>MATERIALS SCIENCE</subject><subject>Proteins - chemistry</subject><subject>Small Molecule Libraries</subject><subject>Synchrotron radiation</subject><issn>1047-8477</issn><issn>1095-8657</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNp9kU2L1TAUhosozof-ADcSXLnpNd9pcSWDzggDbnQd0vT0NqVNapIKd36Iv9fUO85SOCQH8uTlnPetqjcEHwgm8sN0mFJ3oJiIAy6F5bPqkuBW1I0U6vnec1U3XKmL6iqlCWPMCSUvqwsqMVW8UZfV7zt3HFEeY9iO47pllGwE8M4f0Zb209iwpews6mNYZ8gIJrDZBY9yQDYsnfOA1hgyOI9sPKVs5oSM75EdYXHWzGh2XTTRQULhCZndg_mrss4mlxeT0bhP0oNPLp9eVS-GogOvH-_r6seXz99v7ur7b7dfbz7d15a3LNeEiUY1UMxoeDtQxmhrm5ZRZcUgBeey4bwHMMRiyqArdhghQElqGBUDw-y6enfWDWVHnazLYEcbvC87akIFZkIW6P0ZKmv-3CBlvbhkYZ6Nh2KOJrJlihFJSUHJGbUxpBRh0Gt0i4knTbDeM9OTLpnpPTONS-Fd_u2j_NYt0D_9-BdSAT6eAShO_HIQ90HBW-hd3Ofsg_uP_B8xxalQ</recordid><startdate>20150701</startdate><enddate>20150701</enddate><creator>Teplitsky, Ella</creator><creator>Joshi, Karan</creator><creator>Ericson, Daniel L.</creator><creator>Scalia, Alexander</creator><creator>Mullen, Jeffrey D.</creator><creator>Sweet, Robert M.</creator><creator>Soares, Alexei S.</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>OTOTI</scope><orcidid>https://orcid.org/0000-0003-2822-771X</orcidid><orcidid>https://orcid.org/000000032822771X</orcidid></search><sort><creationdate>20150701</creationdate><title>High throughput screening using acoustic droplet ejection to combine protein crystals and chemical libraries on crystallization plates at high density</title><author>Teplitsky, Ella ; 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subjects | Acoustic droplet ejection Chemical biology Crystallization Crystallography Crystallography, X-Ray Drug Discovery Fragment screening High throughput screening In situ X-ray data collection MATERIALS SCIENCE Proteins - chemistry Small Molecule Libraries Synchrotron radiation |
title | High throughput screening using acoustic droplet ejection to combine protein crystals and chemical libraries on crystallization plates at high density |
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