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高通量蛋白质结晶

High-throughput protein crystallization.

作者信息

Stevens R C

机构信息

The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.

出版信息

Curr Opin Struct Biol. 2000 Oct;10(5):558-63. doi: 10.1016/s0959-440x(00)00131-7.

Abstract

The combinatorial chemistry industry has made major advances in the handling and mixing of small volumes, and in the development of robust liquid-handling systems. In addition, developments have been made in the area of material handling for the high-throughput drug screening and combinatorial chemistry fields. Lastly, improvements in beamline optics at synchrotron sources have enabled the use of flash-frozen micron-sized (10-50 microm) crystals. The combination of these and other recent advances will make high-throughput protein crystallography possible. Further advances in high-throughput methods of protein crystallography will require application of the above developments and the accumulation of success/failure data in a more systematic manner. Major changes in crystallography technology will emerge based on the data collected by first-generation high-throughput systems.

摘要

组合化学行业在小体积物质的处理与混合以及稳健的液体处理系统开发方面取得了重大进展。此外,在高通量药物筛选和组合化学领域的材料处理方面也有了发展。最后,同步加速器光源处束线光学的改进使得使用快速冷冻的微米级(10 - 50微米)晶体成为可能。这些进展与其他近期进展相结合将使高通量蛋白质晶体学成为可能。蛋白质晶体学高通量方法的进一步进展将需要以上述发展成果为基础,并更系统地积累成功/失败数据。基于第一代高通量系统收集的数据,晶体学技术将出现重大变革。

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