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瑞士光源的快速片段筛选和组合筛选流水线。

Fast fragment- and compound-screening pipeline at the Swiss Light Source.

机构信息

Swiss Light Source, Paul Scherrer Institute, 5232 Villigen PSI, Switzerland.

Department of Cellular Microbiology, Institute of Biology, University of Hohenheim, 70599 Stuttgart, Germany.

出版信息

Acta Crystallogr D Struct Biol. 2022 Mar 1;78(Pt 3):328-336. doi: 10.1107/S2059798322000705. Epub 2022 Feb 21.

Abstract

Over the last two decades, fragment-based drug discovery (FBDD) has emerged as an effective and efficient method to identify new chemical scaffolds for the development of lead compounds. X-ray crystallography can be used in FBDD as a tool to validate and develop fragments identified as binders by other methods. However, it is also often used with great success as a primary screening technique. In recent years, technological advances at macromolecular crystallography beamlines in terms of instrumentation, beam intensity and robotics have enabled the development of dedicated platforms at synchrotron sources for FBDD using X-ray crystallography. Here, the development of the Fast Fragment and Compound Screening (FFCS) platform, an integrated next-generation pipeline for crystal soaking, handling and data collection which allows crystallography-based screening of protein crystals against hundreds of fragments and compounds, at the Swiss Light Source is reported.

摘要

在过去的二十年中,碎片药物发现(FBDD)已经成为一种有效的方法,可以识别新的化学支架,用于开发先导化合物。X 射线晶体学可用于 FBDD,作为通过其他方法鉴定为结合物的碎片的验证和开发工具。然而,它也经常被成功地用作主要筛选技术。近年来,在大分子晶体学光束线上的技术进步,包括仪器、光束强度和机器人方面,使得在同步加速器源上开发用于 X 射线晶体学的 FBDD 的专用平台成为可能。在这里,报道了瑞士光源上的 Fast Fragment and Compound Screening(FFCS)平台的开发情况,这是一个集成的下一代管道,用于晶体浸泡、处理和数据收集,允许对蛋白质晶体进行基于晶体学的筛选,以对抗数百种碎片和化合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d41/8900825/c371d0c5a2d8/d-78-00328-fig1.jpg

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