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自上而下的蛋白质组学揭示了急性心肌梗死后肌丝和Z盘蛋白磷酸化的协同降低。

Top-down proteomics reveals concerted reductions in myofilament and Z-disc protein phosphorylation after acute myocardial infarction.

作者信息

Peng Ying, Gregorich Zachery R, Valeja Santosh G, Zhang Han, Cai Wenxuan, Chen Yi-Chen, Guner Huseyin, Chen Albert J, Schwahn Denise J, Hacker Timothy A, Liu Xiaowen, Ge Ying

机构信息

From the ‡Department of Cell and Regenerative Biology, University of Wisconsin-Madison, 1300 University Ave., Madison, Wisconsin 53706;

From the ‡Department of Cell and Regenerative Biology, University of Wisconsin-Madison, 1300 University Ave., Madison, Wisconsin 53706; §Molecular Pharmacology Training Program, University of Wisconsin-Madison, 1300 University Ave., Madison, Wisconsin 53706;

出版信息

Mol Cell Proteomics. 2014 Oct;13(10):2752-64. doi: 10.1074/mcp.M114.040675. Epub 2014 Jun 26.

Abstract

Heart failure (HF) is a leading cause of morbidity and mortality worldwide and is most often precipitated by myocardial infarction. However, the molecular changes driving cardiac dysfunction immediately after myocardial infarction remain poorly understood. Myofilament proteins, responsible for cardiac contraction and relaxation, play critical roles in signal reception and transduction in HF. Post-translational modifications of myofilament proteins afford a mechanism for the beat-to-beat regulation of cardiac function. Thus it is of paramount importance to gain a comprehensive understanding of post-translational modifications of myofilament proteins involved in regulating early molecular events in the post-infarcted myocardium. We have developed a novel liquid chromatography-mass spectrometry-based top-down proteomics strategy to comprehensively assess the modifications of key cardiac proteins in the myofilament subproteome extracted from a minimal amount of myocardial tissue with high reproducibility and throughput. The entire procedure, including tissue homogenization, myofilament extraction, and on-line LC/MS, takes less than three hours. Notably, enabled by this novel top-down proteomics technology, we discovered a concerted significant reduction in the phosphorylation of three crucial cardiac proteins in acutely infarcted swine myocardium: cardiac troponin I and myosin regulatory light chain of the myofilaments and, unexpectedly, enigma homolog isoform 2 (ENH2) of the Z-disc. Furthermore, top-down MS allowed us to comprehensively sequence these proteins and pinpoint their phosphorylation sites. For the first time, we have characterized the sequence of ENH2 and identified it as a phosphoprotein. ENH2 is localized at the Z-disc, which has been increasingly recognized for its role as a nodal point in cardiac signaling. Thus our proteomics discovery opens up new avenues for the investigation of concerted signaling between myofilament and Z-disc in the early molecular events that contribute to cardiac dysfunction and progression to HF.

摘要

心力衰竭(HF)是全球发病和死亡的主要原因,最常见的诱因是心肌梗死。然而,心肌梗死后立即导致心脏功能障碍的分子变化仍知之甚少。肌丝蛋白负责心脏的收缩和舒张,在HF的信号接收和转导中起关键作用。肌丝蛋白的翻译后修饰为心脏功能的逐搏调节提供了一种机制。因此,全面了解参与调节梗死心肌早期分子事件的肌丝蛋白的翻译后修饰至关重要。我们开发了一种基于液相色谱-质谱的新型自上而下蛋白质组学策略,以高重现性和通量全面评估从少量心肌组织中提取的肌丝亚蛋白质组中关键心脏蛋白的修饰。整个过程,包括组织匀浆、肌丝提取和在线LC/MS,耗时不到三小时。值得注意的是,通过这种新型自上而下蛋白质组学技术,我们发现急性梗死猪心肌中三种关键心脏蛋白的磷酸化显著协同降低:肌钙蛋白I、肌丝的肌球蛋白调节轻链,以及出乎意料的Z盘的谜同源异构体2(ENH2)。此外,自上而下的质谱使我们能够全面测序这些蛋白质并确定其磷酸化位点。我们首次对ENH2的序列进行了表征,并将其鉴定为一种磷蛋白。ENH2定位于Z盘,其作为心脏信号传导中的节点作用越来越受到认可。因此,我们的蛋白质组学发现为研究肌丝和Z盘之间在导致心脏功能障碍和进展为HF的早期分子事件中的协同信号传导开辟了新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11a7/4189000/65953affb475/zjw0101448400001.jpg

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