Whitten Andrew E, Trewhella Jill
Bragg Institute, Australian Nuclear Science and Technology Organisation, Lucas Heights, N.S.W., Australia.
Methods Mol Biol. 2009;544:307-23. doi: 10.1007/978-1-59745-483-4_20.
Structural molecular biology over the past several decades has progressed from studies of the individual proteins, subunits, and domains that accomplish specific biochemistry to seeking to understand the dynamic bio-molecular complexes and assemblies that are responsible for biological function. This progress has led to an expansion of the structural analysis "tool box" to include methods that complement the mainstay techniques of the field: X-ray crystallography, nuclear magnetic resonance (NMR), and cryo-electron microscopy. Small-angle scattering of X-rays or neutrons is one such complementary technique that provides information on the size and shape of scattering particles in solution. This low-resolution structural information can be a powerful complement to high-resolution structural data, especially for the study of bio-molecular interactions with ligands or each other. Further, exploitation of the different neutron-scattering properties of the stable isotopes of hydrogen ((1)H and (2)H) can be used to enrich the information available from the small-angle scattering data, especially for bio-molecular complexes.
在过去几十年中,结构分子生物学已从对执行特定生物化学功能的单个蛋白质、亚基和结构域的研究,发展到试图理解负责生物功能的动态生物分子复合物和组装体。这一进展使得结构分析“工具箱”得以扩展,纳入了补充该领域主流技术(X射线晶体学、核磁共振(NMR)和冷冻电子显微镜)的方法。X射线或中子的小角散射就是这样一种补充技术,它能提供溶液中散射颗粒的大小和形状信息。这种低分辨率结构信息可以成为高分辨率结构数据的有力补充,特别是在研究生物分子与配体或彼此之间的相互作用时。此外,利用氢的稳定同位素((1)H和(2)H)不同的中子散射特性,可用于丰富从小角散射数据中获得的信息,特别是对于生物分子复合物。