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用化学交联和质谱技术定量蛋白质-蛋白质相互作用。

Quantification of protein-protein interactions with chemical cross-linking and mass spectrometry.

机构信息

Department of Genome Sciences, University of Washington, PO Box 358050, Seattle, Washington 98195, United States.

出版信息

J Proteome Res. 2011 Apr 1;10(4):1528-37. doi: 10.1021/pr100898e. Epub 2011 Feb 18.

Abstract

Chemical cross-linking in combination with mass spectrometry has largely been used to study protein structures and protein-protein interactions. Typically, it is used in a qualitative manner to identify cross-linked sites and provide a low-resolution topological map of the interacting regions of proteins. Here, we investigate the capability of chemical cross-linking to quantify protein-protein interactions using a model system of calmodulin and substrates melittin and mastoparan. Calmodulin is a well-characterized protein which has many substrates. Melittin and mastoparan are two such substrates which bind to calmodulin in 1:1 ratios in the presence of calcium. Both the calmodulin-melittin and calmodulin-mastoparan complexes have had chemical cross-linking strategies successfully applied in the past to investigate topological properties. We utilized an excess of immobilized calmodulin on agarose beads and formed complexes with varying quantities of mastoparan and melittin. Then, we applied disuccinimidyl suberate (DSS) chemical cross-linker, digested and detected cross-links through an LC-MS analytical method. We identified five interpeptide cross-links for calmodulin-melittin and three interpeptide cross-links for calmodulin-mastoparan. Using cross-linking sites of calmodulin-mastoparan, we demonstrated that mastoparan also binds in two orientations to calmodulin. We quantitatively demonstrated that both melittin and mastoparan preferentially bind to calmodulin in a parallel fashion, which is opposite to the preferred binding mode of the majority of known calmodulin binding peptides. We also demonstrated that the relative abundances of cross-linked peptide products quantitatively reflected the abundances of the calmodulin peptide complexes formed.

摘要

化学交联结合质谱分析在很大程度上被用于研究蛋白质结构和蛋白质-蛋白质相互作用。通常,它用于定性地识别交联位点,并提供蛋白质相互作用区域的低分辨率拓扑图。在这里,我们使用钙调蛋白和底物蜂毒素和 mastoparan 的模型系统研究了化学交联定量蛋白质-蛋白质相互作用的能力。钙调蛋白是一种特征明确的蛋白质,有许多底物。蜂毒素和 mastoparan 是两种在存在钙的情况下以 1:1 比例与钙调蛋白结合的底物。钙调蛋白-蜂毒素和钙调蛋白-mastoparan 复合物都曾成功地应用化学交联策略来研究拓扑性质。我们利用琼脂糖珠上过量的固定化钙调蛋白与不同数量的 mastoparan 和蜂毒素形成复合物。然后,我们应用二琥珀酰亚胺基琥珀酸酯(DSS)化学交联剂,通过 LC-MS 分析方法消化并检测交联。我们鉴定了钙调蛋白-蜂毒素的五个肽间交联,以及钙调蛋白-mastoparan 的三个肽间交联。利用钙调蛋白-mastoparan 的交联位点,我们证明 mastoparan 也以两种取向与钙调蛋白结合。我们定量证明了蜂毒素和 mastoparan 都优先以平行的方式与钙调蛋白结合,这与大多数已知的钙调蛋白结合肽的首选结合模式相反。我们还证明,交联肽产物的相对丰度定量反映了形成的钙调蛋白肽复合物的丰度。

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