Targeted proteomics of myofilament phosphorylation and other protein posttranslational modifications

被引:12
作者
Ramirez-Correa, Genaro A. [1 ]
Martinez-Ferrando, Maria Isabel [2 ]
Zhang, Pingbo [3 ]
Murphy, Anne M. [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Pediat, Div Cardiol, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Comparat Biol & Pathol, Baltimore, MD USA
[3] Johns Hopkins Univ, Sch Med, Hopkins Bayview Prote Ctr, Baltimore, MD USA
关键词
Cardiac myofilaments; Heart failure; CARDIAC TROPONIN-I; MONITORING MASS-SPECTROMETRY; MUSCLE THIN FILAMENT; KINASE-A; MULTISITE PHOSPHORYLATION; ABSOLUTE QUANTIFICATION; QUANTITATIVE PROTEOMICS; GLCNAC MODIFICATION; MODIFICATION SITES; ASSAY DEVELOPMENT;
D O I
10.1002/prca.201400034
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Global cardiac myofilament protein phosphorylation levels, and their site-specific stoichiometry, are physiologically and clinically relevant for heart function. Unlike myofilament phosphorylation, other PTMs such as O-GlcNAcylation are just beginning to gain attention due to their potential physiological and clinical implications. This review will focus on what is currently known about cardiac troponin I phosphorylation, and on the potential physiological and clinical impact of targeted proteomics including new findings on cardiac troponin I sites and stoichiometry. We will then discuss the increasing recognition of other myofilament PTMs functional relevance and the potential of targeted MS approaches, particularly MRM, for accelerating their systematic characterization. In addition, we will broadly discuss the development and application of MRM to quantitatively assess site-specific PTMs. Finally, we will give an overview of expert's consensus on MRM methods design/validation and best practices to develop MRM assays intended to reach clinical application. The unique ability of MRM and similar methods to identify and quantify cardiac myofilament PTMs is likely to become central in answering important biological questions in the field of cardiac integrative physiology.
引用
收藏
页码:543 / 553
页数:11
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