Comprehensive Characterization of Swine Cardiac Troponin T Proteoforms by Top-Down Mass Spectrometry
Lin, Ziqing3,4; Guo, Fang3,5; Gregorich, Zachery R.3; Sun, Ruixiang3,6; Zhang, Han2; Hu, Yang3; Shanmuganayagam, Dhanansayan1; Ge, Ying2,3,4
刊名JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY
2018-06-01
卷号29期号:6页码:1284-1294
关键词Cardiac troponin Heart disease Proteoform Top-down proteomics Collisionally activated dissociation Electron-transfer dissociation Electron-capture dissociation
ISSN号1044-0305
DOI10.1007/s13361-018-1925-y
英文摘要Cardiac troponin T (cTnT) regulates the Ca2+-mediated interaction between myosin thick filaments and actin thin filaments during cardiac contraction and relaxation. cTnT is released into the blood following injury, and increased serum levels of the protein are used clinically as a biomarker for myocardial infarction. Moreover, mutations in cTnT are causative in a number of familial cardiomyopathies. With the increasing use of large animal (swine) model to recapitulate human diseases, it is essential to characterize species-dependent protein sequence variants, alternative RNA splicing, and post-translational modifications (PTMs), but challenges remain due to the incomplete database and lack of validation of the predicted splicing isoforms. Herein, we integrated top-down mass spectrometry (MS) with online liquid chromatography (LC) and immunoaffinity purification to comprehensively characterize miniature swine cTnT proteoforms, including those arising from alternative RNA splicing and PTMs. A total of seven alternative splicing isoforms of cTnT were identified by LC/MS from swine left ventricular tissue, with each isoform containing un-phosphorylated and mono-phosphorylated proteoforms. The phosphorylation site was localized to Ser1 for the mono-phosphorylated proteoforms of cTnT1, 3, 4, and 6 by online MS/MS combining collisionally activated dissociation (CAD) and electron transfer dissociation (ETD). Offline MS/MS on Fourier-transform ion cyclotron resonance (FT-ICR) mass spectrometer with CAD and electron capture dissociation (ECD) was then utilized to achieve deep sequencing of mono-phosphorylated cTnT1 (35.2 kDa) with a high sequence coverage of 87%. Taken together, this study demonstrated the unique advantage of top-down MS in the comprehensive characterization of protein alternative splicing isoforms together with PTMs.
资助项目NIH[R01 HL109810] ; NIH[HL096971] ; NIH[R01 GM117058] ; NIH[S10 OD018475]
WOS研究方向Biochemistry & Molecular Biology ; Chemistry ; Spectroscopy
语种英语
出版者SPRINGER
WOS记录号WOS:000435538300021
内容类型期刊论文
源URL[http://119.78.100.204/handle/2XEOYT63/5107]  
专题中国科学院计算技术研究所期刊论文_英文
通讯作者Ge, Ying
作者单位1.Univ Wisconsin, Dept Anim Sci, Madison, WI 53706 USA
2.Univ Wisconsin, Dept Chem, 1101 Univ Ave, Madison, WI 53706 USA
3.Univ Wisconsin, Dept Cell & Regenerat Biol, Madison, WI 53705 USA
4.Univ Wisconsin, Human Prote Program, Madison, WI 53705 USA
5.Shandong Prov Hosp, Dept Cardiol, Jinan 250021, Shandong, Peoples R China
6.Chinese Acad Sci, Inst Comp Technol, Beijing 100190, Peoples R China
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Lin, Ziqing,Guo, Fang,Gregorich, Zachery R.,et al. Comprehensive Characterization of Swine Cardiac Troponin T Proteoforms by Top-Down Mass Spectrometry[J]. JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY,2018,29(6):1284-1294.
APA Lin, Ziqing.,Guo, Fang.,Gregorich, Zachery R..,Sun, Ruixiang.,Zhang, Han.,...&Ge, Ying.(2018).Comprehensive Characterization of Swine Cardiac Troponin T Proteoforms by Top-Down Mass Spectrometry.JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY,29(6),1284-1294.
MLA Lin, Ziqing,et al."Comprehensive Characterization of Swine Cardiac Troponin T Proteoforms by Top-Down Mass Spectrometry".JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY 29.6(2018):1284-1294.
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