Tang Xiaoting, Bruce James E
Novo Nordisk Inflammation Research Center, Seattle, Washington, USA.
Mol Biosyst. 2010 Jun;6(6):939-47. doi: 10.1039/b920876c. Epub 2010 Mar 16.
Chemical cross-linking coupled with mass spectrometry, an emerging approach for protein topology and interaction studies, has gained increasing interest in the past few years. A number of recent proof-of-principle studies on model proteins or protein complex systems with improved cross-linking strategies have shown great promise. However, the heterogeneity and low abundance of the cross-linked products as well as data complexity continue to pose enormous challenges for large-scale application of cross-linking approaches. A novel mass spectrometry-cleavable cross-linking strategy embodied in Protein Interaction Reporter (PIR) technology, first reported in 2005, was recently successfully applied for in vivo identification of protein-protein interactions as well as actual regions of the interacting proteins that share close proximity while present within cells. PIR technology holds great promise for achieving the ultimate goal of mapping protein interaction network at systems level using chemical cross-linking. In this review, we will briefly describe the recent progress in the field of chemical cross-linking development with an emphasis on the PIR concepts, its applications and future directions.
化学交联结合质谱分析是一种用于蛋白质拓扑结构和相互作用研究的新兴方法,在过去几年中受到了越来越多的关注。最近,一些针对模型蛋白或蛋白质复合物系统开展的原理验证研究采用了改进的交联策略,展现出了巨大的潜力。然而,交联产物的异质性、低丰度以及数据的复杂性,仍然给交联方法的大规模应用带来了巨大挑战。2005年首次报道的蛋白质相互作用报告分子(PIR)技术所体现的一种新型质谱可裂解交联策略,最近成功应用于体内蛋白质-蛋白质相互作用的鉴定,以及细胞内相互靠近的相互作用蛋白的实际区域的鉴定。PIR技术对于利用化学交联在系统水平绘制蛋白质相互作用网络这一最终目标的实现具有巨大潜力。在这篇综述中,我们将简要描述化学交联发展领域的最新进展,重点介绍PIR概念、其应用及未来方向。