Wellcome Trust Centre for Cell Biology, University of Edinburgh, Michael Swann Building, King's Buildings, Mayfield Road, Edinburgh, EH9 3JR Scotland, UK.
J Struct Biol. 2011 Mar;173(3):530-40. doi: 10.1016/j.jsb.2010.10.014. Epub 2010 Oct 26.
After more than a decade of method development, cross-linking in combination with mass spectrometry and bioinformatics is finally coming of age. This technology now provides improved opportunities for modelling by mapping structural details of functional complexes in solution. The structure of proteins or protein complexes is ascertained by identifying amino acid pairs that are positioned in close proximity to each other. The validity of this technique has recently been benchmarked for large multi-protein complexes, by comparing cross-link data with that from a crystal structure of RNA polymerase II. Here, the specific nature of this cross-linking data will be discussed to assess the technical challenges and opportunities for model building. We believe that once remaining technological challenges of cross-linking/mass spectrometry have been addressed and cross-linking/mass spectrometry data has been incorporated into modelling algorithms it will quickly become an indispensable companion of protein and protein complex modelling and a corner-stone of integrated structural biology.
经过十多年的方法开发,交联技术结合质谱和生物信息学终于迎来了发展的黄金时期。该技术现在为通过绘制溶液中功能复合物的结构细节来进行建模提供了更好的机会。通过鉴定彼此位置接近的氨基酸对,可以确定蛋白质或蛋白质复合物的结构。最近,通过将交联数据与 RNA 聚合酶 II 的晶体结构数据进行比较,对大型多蛋白复合物的这种技术的有效性进行了基准测试。在这里,将讨论这种交联数据的具体性质,以评估模型构建的技术挑战和机遇。我们相信,一旦交联/质谱技术的剩余技术挑战得到解决,并且交联/质谱数据被纳入建模算法中,它将迅速成为蛋白质和蛋白质复合物建模不可或缺的伴侣,以及整合结构生物学的基石。