Literature DB >> 11815235

High-throughput crystallization and structure determination in drug discovery.

Lance Stewart1, Robin Clark, Craig Behnke.   

Abstract

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.

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Year:  2002        PMID: 11815235     DOI: 10.1016/s1359-6446(01)02121-3

Source DB:  PubMed          Journal:  Drug Discov Today        ISSN: 1359-6446            Impact factor:   7.851


  8 in total

1.  The mechanism of topoisomerase I poisoning by a camptothecin analog.

Authors:  Bart L Staker; Kathryn Hjerrild; Michael D Feese; Craig A Behnke; Alex B Burgin; Lance Stewart
Journal:  Proc Natl Acad Sci U S A       Date:  2002-11-08       Impact factor: 11.205

Review 2.  Protein crystallization for genomics: throughput versus output.

Authors:  Naomi E Chayen
Journal:  J Struct Funct Genomics       Date:  2003

3.  An automated system to mount cryo-cooled protein crystals on a synchrotron beam line, using compact sample cassettes and a small-scale robot.

Authors:  Aina E Cohen; Paul J Ellis; Mitchell D Miller; Ashley M Deacon; R Paul Phizackerley
Journal:  J Appl Crystallogr       Date:  2002-12       Impact factor: 3.304

4.  Molecular recognition in the case of flexible targets.

Authors:  Anthony Ivetac; J Andrew McCammon
Journal:  Curr Pharm Des       Date:  2011       Impact factor: 3.116

5.  An efficient strategy for high-throughput expression screening of recombinant integral membrane proteins.

Authors:  Said Eshaghi; Marie Hedrén; Marina Ignatushchenko Abdel Nasser; Tove Hammarberg; Anders Thornell; Pär Nordlund
Journal:  Protein Sci       Date:  2005-02-02       Impact factor: 6.725

6.  Functional repertoire, molecular pathways and diseases associated with 3D domain swapping in the human proteome.

Authors:  Khader Shameer; Ramanathan Sowdhamini
Journal:  J Clin Bioinforma       Date:  2012-04-03

7.  Large-scale Direct Targeting for Drug Repositioning and Discovery.

Authors:  Chunli Zheng; Zihu Guo; Chao Huang; Ziyin Wu; Yan Li; Xuetong Chen; Yingxue Fu; Jinlong Ru; Piar Ali Shar; Yuan Wang; Yonghua Wang
Journal:  Sci Rep       Date:  2015-07-09       Impact factor: 4.379

8.  Two Methods, One Goal: Structural Differences between Cocrystallization and Crystal Soaking to Discover Ligand Binding Poses.

Authors:  Barbara Wienen-Schmidt; Matthias Oebbeke; Khang Ngo; Andreas Heine; Gerhard Klebe
Journal:  ChemMedChem       Date:  2020-10-30       Impact factor: 3.466

  8 in total

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