| Literature DB >> 27020925 |
David Z Keifer1, Tina Motwani2, Carolyn M Teschke2,3, Martin F Jarrold4.
Abstract
Charge detection mass spectrometry (CDMS) is a single-molecule technique particularly well-suited to measuring the mass and charge distributions of heterogeneous, MDa-sized ions. In this work, CDMS has been used to analyze the assembly products of two coat protein variants of bacteriophage P22. The assembly products show broad mass distributions extending from 5 to 15 MDa for A285Y and 5 to 25 MDa for A285T coat protein variants. Because the charge of large ions generated by electrospray ionization depends on their size, the charge can be used to distinguish hollow shells from more compact structures. A285T was found to form T = 4 and T = 7 procapsids, and A285Y makes a small number of T = 3 and T = 4 procapsids. Owing to the decreased stability of the A285Y and A285T particles, chemical cross-linking was required to stabilize them for electrospray CDMS.Graphical Abstract.Entities:
Keywords: Bacteriophage P22; Charge detection mass spectrometry; Coat protein; Procapsid; Virus capsid
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Year: 2016 PMID: 27020925 PMCID: PMC5095694 DOI: 10.1007/s13361-016-1362-8
Source DB: PubMed Journal: J Am Soc Mass Spectrom ISSN: 1044-0305 Impact factor: 3.109