Brutscher Bernhard, Lescop Ewen
Institut de Biologie Structurale - Jean-Pierre Ebel, CNRS, CEA, UJF, UMR5075, Grenoble Cedex, France.
Methods Mol Biol. 2012;831:407-28. doi: 10.1007/978-1-61779-480-3_21.
Probing protein structure, dynamics, and interaction surfaces by NMR requires initial backbone resonance assignment. The protocol for this step has been progressively developed in the last 15 years to provide robust assignments. However, even in the case of favorable conditions (high field magnets and cryogenically cooled probes, small globular proteins, high sample concentration), the assignment step generally takes several days of data collection and analysis, thus precluding studies of unstable proteins and limiting high-throughput applications. Recently, we have introduced the BATCH strategy for fast protein backbone resonance assignment. BATCH benefits from the combination of several tools (BEST/ASCOM/Targeted-Sampling/COBRA/HADAMAC) for time-optimized and highly automated NMR data acquisition, processing, and analysis. In this chapter, we discuss the individual steps of the BATCH method and describe its practical implementation to obtain the backbone resonance assignment of small globular proteins in a few hours of time.
通过核磁共振(NMR)探测蛋白质结构、动力学和相互作用表面需要首先进行主链共振归属。在过去15年中,这一步骤的方案已逐步发展以提供可靠的归属。然而,即使在有利条件下(高场磁体和低温冷却探头、小分子球状蛋白质、高样品浓度),归属步骤通常也需要几天的数据收集和分析,因此排除了对不稳定蛋白质的研究并限制了高通量应用。最近,我们引入了用于快速蛋白质主链共振归属的BATCH策略。BATCH受益于多种工具(BEST/ASCOM/靶向采样/COBRA/HADAMAC)的组合,用于时间优化和高度自动化的NMR数据采集、处理和分析。在本章中,我们讨论BATCH方法的各个步骤,并描述其实际应用,以便在几小时内获得小分子球状蛋白质的主链共振归属。