High-throughput crystallization and structure determination in drug discovery
High-throughput protein X-ray crystallography offers an unprecedented opportunity to facilitate drug discovery. The key bottlenecks in the path from target gene to three-dimensional protein structure determination are defined. Special emphasis is placed on the concept that drug discovery projects ar...
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Veröffentlicht in: | Drug Discovery Today 2002-02, Vol.7 (3), p.187-196 |
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container_title | Drug Discovery Today |
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creator | Stewart, Lance Clark, Robin Behnke, Craig |
description | High-throughput protein X-ray crystallography offers an unprecedented opportunity to facilitate drug discovery. The key bottlenecks in the path from target gene to three-dimensional protein structure determination are defined. Special emphasis is placed on the concept that drug discovery projects are typically directed at a key protein target whose structure must be solved within a reasonable time frame to have an impact on the drug discovery process. The time-sensitive nature of structural data has placed growing pressure on the need to automate all aspects of protein crystallography, from gene identification to model building and refinement. Current technological innovations and strategies for automation are discussed with respect to the bottleneck they are intended to eliminate. |
doi_str_mv | 10.1016/S1359-6446(01)02121-3 |
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The key bottlenecks in the path from target gene to three-dimensional protein structure determination are defined. Special emphasis is placed on the concept that drug discovery projects are typically directed at a key protein target whose structure must be solved within a reasonable time frame to have an impact on the drug discovery process. The time-sensitive nature of structural data has placed growing pressure on the need to automate all aspects of protein crystallography, from gene identification to model building and refinement. 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The key bottlenecks in the path from target gene to three-dimensional protein structure determination are defined. Special emphasis is placed on the concept that drug discovery projects are typically directed at a key protein target whose structure must be solved within a reasonable time frame to have an impact on the drug discovery process. The time-sensitive nature of structural data has placed growing pressure on the need to automate all aspects of protein crystallography, from gene identification to model building and refinement. Current technological innovations and strategies for automation are discussed with respect to the bottleneck they are intended to eliminate.</description><subject>Automation</subject><subject>Biological and medical sciences</subject><subject>Cloning, Molecular</subject><subject>crystallization</subject><subject>Crystallography, X-Ray - methods</subject><subject>Databases, Factual</subject><subject>Drug Design</subject><subject>General pharmacology</subject><subject>ligand-protein co-crystals</subject><subject>Medical sciences</subject><subject>Models, Chemical</subject><subject>Molecular Conformation</subject><subject>Pharmaceutical technology. Pharmaceutical industry</subject><subject>Pharmacology - methods</subject><subject>Pharmacology. Drug treatments</subject><subject>protein structure</subject><subject>Proteins - chemistry</subject><subject>Quality Control</subject><subject>X-ray</subject><issn>1359-6446</issn><issn>1878-5832</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMFu2zAMhoWhxZJ1e4QWvrRYD95EyZLlU1EU3VogxQ7bzoIs0YkGx84kOUD69HXqFD3mRAL8SP74CDkH-g0oyO-_gYsql0Uhv1K4pgwY5PwDmYMqVS4UZydj_4bMyKcY_1EKrBLyI5kBKBCMizl5evDLVZ5WoR-Wq82QMht2MZm29c8m-b7LTOeymMJg0xAwc5gwrH03zXyXuTAsM-ej7bcYdp_JaWPaiF8O9Yz8_XH_5-4hX_z6-Xh3u8htoVTKCypZLVzDURVYjkXK2lGGdWWkFExVtVFKQEONrFyJJWfWgqS1LCQVQA0_I1fT3U3o_w8Yk16PEbBtTYf9EHXJykpJpo6CoHg5vuQjKCbQhj7GgI3eBL82YaeB6r1w_Spc721qCvpVuN7vXRweDPUa3fvWwfAIXB4AE61pm2A66-M7xwteMFqO3M3E4eht6zHoaD12Fp0PaJN2vT8S5QUC_J1R</recordid><startdate>20020201</startdate><enddate>20020201</enddate><creator>Stewart, Lance</creator><creator>Clark, Robin</creator><creator>Behnke, Craig</creator><general>Elsevier Ltd</general><general>Elsevier Science</general><scope>IQODW</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>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20020201</creationdate><title>High-throughput crystallization and structure determination in drug discovery</title><author>Stewart, Lance ; Clark, Robin ; Behnke, Craig</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c488t-4062b5df3e84e7f3e66bd02eb9a665289ba8851f0a69d7e732cc160b6460510a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Automation</topic><topic>Biological and medical sciences</topic><topic>Cloning, Molecular</topic><topic>crystallization</topic><topic>Crystallography, X-Ray - methods</topic><topic>Databases, Factual</topic><topic>Drug Design</topic><topic>General pharmacology</topic><topic>ligand-protein co-crystals</topic><topic>Medical sciences</topic><topic>Models, Chemical</topic><topic>Molecular Conformation</topic><topic>Pharmaceutical technology. Pharmaceutical industry</topic><topic>Pharmacology - methods</topic><topic>Pharmacology. Drug treatments</topic><topic>protein structure</topic><topic>Proteins - chemistry</topic><topic>Quality Control</topic><topic>X-ray</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stewart, Lance</creatorcontrib><creatorcontrib>Clark, Robin</creatorcontrib><creatorcontrib>Behnke, Craig</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Drug Discovery Today</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stewart, Lance</au><au>Clark, Robin</au><au>Behnke, Craig</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>High-throughput crystallization and structure determination in drug discovery</atitle><jtitle>Drug Discovery Today</jtitle><addtitle>Drug Discov Today</addtitle><date>2002-02-01</date><risdate>2002</risdate><volume>7</volume><issue>3</issue><spage>187</spage><epage>196</epage><pages>187-196</pages><issn>1359-6446</issn><eissn>1878-5832</eissn><abstract>High-throughput protein X-ray crystallography offers an unprecedented opportunity to facilitate drug discovery. 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subjects | Automation Biological and medical sciences Cloning, Molecular crystallization Crystallography, X-Ray - methods Databases, Factual Drug Design General pharmacology ligand-protein co-crystals Medical sciences Models, Chemical Molecular Conformation Pharmaceutical technology. Pharmaceutical industry Pharmacology - methods Pharmacology. Drug treatments protein structure Proteins - chemistry Quality Control X-ray |
title | High-throughput crystallization and structure determination in drug discovery |
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