Aprotinin

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CAS: 9087-70-1
MF: C284H432N84O79S7
MW: 6511.43928
Synonyms: Aprotinin

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Mingdong Huang

Chinese Academy of Sciences
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Jinping Zhou

Wuhan University
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Ping Zhou

Wuhan University
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Hongying Zhong

Central China Normal University
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Bing Yan

Shandong University
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Chinedum O. Osuji

Yale University
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Laura J. Kaufman

Columbia University
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Nikolai R. Skrynnikov

Purdue University
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Charles S. Craik

University of California
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Ying Ge

University of Wisconsin?Madison
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Co-reporter: Bifan Chen, Ying Peng, Santosh G. Valeja, Lichen Xiu, Andrew J. Alpert, and Ying Ge
pp: 1885
Publication Date(Web):January 5, 2016
DOI: 10.1021/acs.analchem.5b04285
Recent progress in top-down proteomics has led to a demand for mass spectrometry (MS)-compatible chromatography techniques to separate intact proteins using volatile mobile phases. Conventional hydrophobic interaction chromatography (HIC) provides high-resolution separation of proteins under nondenaturing conditions but requires high concentrations of nonvolatile salts. Herein, we introduce a series of more-hydrophobic HIC materials that can retain proteins using MS-compatible concentrations of ammonium acetate. The new HIC materials appear to function as a hybrid form of conventional HIC and reverse phase chromatography. The function of the salt seems to be preserving protein structure rather than promoting retention. Online HIC-MS is feasible for both qualitative and quantitative analysis. This is demonstrated with standard proteins and a complex cell lysate. The mass spectra of proteins from the online HIC-MS exhibit low charge-state distributions, consistent with those commonly observed in native MS. Furthermore, HIC-MS can chromatographically separate proteoforms differing by minor modifications. Hence, this new HIC-MS combination is promising for top-down proteomics.