Literature DB >> 30390801

Achieving a Good Crystal System for Crystallographic X-Ray Fragment Screening.

Patrick M Collins1, Alice Douangamath1, Romain Talon1, Alexandre Dias1, Jose Brandao-Neto1, Tobias Krojer2, Frank von Delft3.   

Abstract

The XChem facility at Diamond Light Source offers fragment screening by X-ray crystallography as a general access user program. The main advantage of X-ray crystallography as a primary fragment screen is that it yields directly the location and pose of the fragment hits, whether within pockets of interest or merely on surface sites: this is the key information for structure-based design and for enabling synthesis of follow-up molecules. Extensive streamlining of the screening experiment at XChem has engendered a very active user program that is generating large amounts of data: in 2017, 36 academic and industry groups generated 35,000 datasets of uniquely soaked crystals. It has also generated a large number of learnings concerning the main remaining bottleneck, namely, obtaining a suitable crystal system that will support a successful fragment screen. Here we discuss the practicalities of generating screen-ready crystals that have useful electron density maps, and how to ensure they will be successfully reproduced and usable at a facility outside the home lab.
© 2018 Elsevier Inc. All rights reserved.

Keywords:  Diamond Light Source; Fragment screening; I04-1; Protein crystallization; Structural genomics consortium; X-ray crystallography; XChem

Mesh:

Substances:

Year:  2018        PMID: 30390801     DOI: 10.1016/bs.mie.2018.09.027

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN: 0076-6879            Impact factor:   1.600


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