Merkley Eric D, Cort John R, Adkins Joshua N
MS K8-98, Biological Sciences Division, Pacific Northwest National Laboratory, Richland, WA 99352, USA.
J Struct Funct Genomics. 2013 Sep;14(3):77-90. doi: 10.1007/s10969-013-9160-z. Epub 2013 Aug 7.
Multiprotein complexes, rather than individual proteins, make up a large part of the biological macromolecular machinery of a cell. Understanding the structure and organization of these complexes is critical to understanding cellular function. Chemical cross-linking coupled with mass spectrometry is emerging as a complementary technique to traditional structural biology methods and can provide low-resolution structural information for a multitude of purposes, such as distance constraints in computational modeling of protein complexes. In this review, we discuss the experimental considerations for successful application of chemical cross-linking-mass spectrometry in biological studies and highlight three examples of such studies from the recent literature. These examples (as well as many others) illustrate the utility of a chemical cross-linking-mass spectrometry approach in facilitating structural analysis of large and challenging complexes.
多蛋白复合物而非单个蛋白质构成了细胞生物大分子机器的很大一部分。理解这些复合物的结构和组织对于理解细胞功能至关重要。化学交联结合质谱分析正在成为传统结构生物学方法的一种补充技术,并且可以为多种目的提供低分辨率的结构信息,例如在蛋白质复合物的计算建模中的距离限制。在本综述中,我们讨论了在生物学研究中成功应用化学交联 - 质谱分析的实验注意事项,并突出了近期文献中此类研究的三个例子。这些例子(以及许多其他例子)说明了化学交联 - 质谱分析方法在促进对大型且具有挑战性的复合物进行结构分析方面的实用性。