Liu Qun, Hendrickson Wayne A
New York Consortium on Membrane Protein Structure, New York Structural Biology Center, New York, NY 10027, USA.
New York Consortium on Membrane Protein Structure, New York Structural Biology Center, New York, NY 10027, USA; Department of Biochemistry and Molecular Biophysics, Columbia University, New York, NY 10032, USA; Department of Physiology and Cellular Biophysics, Columbia University, New York, NY 10032, USA.
Curr Opin Struct Biol. 2015 Oct;34:99-107. doi: 10.1016/j.sbi.2015.08.003. Epub 2015 Sep 30.
The exploitation of anomalous signals for biological structural solution is maturing. Single-wavelength anomalous diffraction (SAD) is dominant in de novo structure analysis. Nevertheless, for challenging structures where the resolution is low (dmin≥3.5Å) or where only lighter atoms (Z≤20) are present, as for native macromolecules, solved SAD structures are still scarce. With the recent rapid development in crystal handling, beamline instrumentation, optimization of data collection strategies, use of multiple crystals and structure determination technologies, the weak anomalous diffraction signals are now robustly measured and should be used for routine SAD structure determination. The review covers these recent advances on weak anomalous signals measurement, analysis and utilization.
利用反常信号求解生物结构的方法正在不断成熟。单波长反常衍射(SAD)在从头结构分析中占据主导地位。然而,对于具有挑战性的结构,如分辨率较低(dmin≥3.5Å)或仅存在较轻原子(Z≤20)的天然大分子结构,已解析的SAD结构仍然很少。随着晶体处理、光束线仪器、数据收集策略优化、多晶体使用和结构测定技术等方面的快速发展,现在可以可靠地测量微弱的反常衍射信号,并应将其用于常规的SAD结构测定。本文综述了这些关于微弱反常信号测量、分析和利用的最新进展。