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Large-Scale Differentiation and Site Specific Discrimination of Hydroxyproline Isomers by Electron Transfer/Higher-Energy Collision Dissociation (EThcD) Mass Spectrometry
Ma, Fengfei1; Sun, Ruixiang2; Tremmel, Daniel M.3; Sacket, Sara Dutton3; Odorico, Jon3; Li, Lingjun1,4
2018-05-01
发表期刊ANALYTICAL CHEMISTRY
ISSN0003-2700
卷号90期号:9页码:5857-5864
摘要3- and 4-Hydroxyprolines (HyP) are regioisomers that play different roles in various species and organs. Despite their distinct functions inside cells, they are generally considered indistinguishable using mass spectrometry due to their identical masses. Here, we demonstrate, for the first time, that characteristic w ions can be produced by electron-transfer/higher energy collision dissociation (EThcD) dual fragmentation technique to confidently discriminate 3-HyP/4-HyP isomers. An integrated and high throughput strategy was developed which combined online LC separation with EThcD for large-scale differentiation of 3-HyP/4-HyP in complex samples. An automated algorithm was developed for charge state dependent characterization of 3-HyP/4-HyP isomers. Using this combined discrimination approach, we identified 108 3-HyP sites and 530 4-HyP sites from decellularized pancreas, allowing more than 5-fold increase of both 3-HyP and 4-HyP identifications compared to previous reports. This approach outperformed ETD and HCD in the analysis of HyP-containing peptides with unique capacity to generate w ions for HyP discrimination, improved fragmentation of precursor ions, as well as unambiguous localization of modifications. A high content of 3-HyP was observed in the C-terminal (GPP)(n) domain of human CO1A1, which was previously only identified in vertebrate fibrillar collagens from tendon. Unexpectedly, some unusual HyP sites at Xaa position in Gly-HyP-Ala, Gly-HyP-Val, Gly-HyP-Gln, Gly-HyP-Ser, and Gly-HyP-Arg were also confirmed to be 3-hydroxylated, whose functions and enzymes are yet to be discovered. Overall, this novel discrimination strategy can be readily implemented into de novo sequencing or other proteomic search engines.
DOI10.1021/acs.analchem8b00413
收录类别SCI
语种英语
资助项目National Institutes of Health[R21AI126419] ; National Institutes of Health[R01DK071801] ; National Institutes of Health[R01AG052324] ; National Institutes of Health[P41GM108538] ; NIH[NIH-NCRR S10RR029531] ; Office of the Vice Chancellor for Research and Graduate Education at the University of Wisconsin-Madison ; Wisconsin Alumni Research Foundation ; University of Wisconsin-Madison School of Pharmacy
WOS研究方向Chemistry
WOS类目Chemistry, Analytical
WOS记录号WOS:000431464400047
出版者AMER CHEMICAL SOC
引用统计
被引频次:12[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符http://119.78.100.204/handle/2XEOYT63/5320
专题中国科学院计算技术研究所期刊论文_英文
通讯作者Li, Lingjun
作者单位1.Univ Wisconsin, Sch Pharm, Madison, WI 53705 USA
2.Chinese Acad Sci, Inst Comp Technol, Beijing 100190, Peoples R China
3.Univ Wisconsin, Sch Med & Publ Hlth, Dept Surg, Div Transplantat, Madison, WI 53705 USA
4.Univ Wisconsin, Dept Chem, 1101 Univ Ave, Madison, WI 53706 USA
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Ma, Fengfei,Sun, Ruixiang,Tremmel, Daniel M.,et al. Large-Scale Differentiation and Site Specific Discrimination of Hydroxyproline Isomers by Electron Transfer/Higher-Energy Collision Dissociation (EThcD) Mass Spectrometry[J]. ANALYTICAL CHEMISTRY,2018,90(9):5857-5864.
APA Ma, Fengfei,Sun, Ruixiang,Tremmel, Daniel M.,Sacket, Sara Dutton,Odorico, Jon,&Li, Lingjun.(2018).Large-Scale Differentiation and Site Specific Discrimination of Hydroxyproline Isomers by Electron Transfer/Higher-Energy Collision Dissociation (EThcD) Mass Spectrometry.ANALYTICAL CHEMISTRY,90(9),5857-5864.
MLA Ma, Fengfei,et al."Large-Scale Differentiation and Site Specific Discrimination of Hydroxyproline Isomers by Electron Transfer/Higher-Energy Collision Dissociation (EThcD) Mass Spectrometry".ANALYTICAL CHEMISTRY 90.9(2018):5857-5864.
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