Literature DB >> 10689670

Gas phase H/D exchange kinetics: DI versus D2O.

T G Schaaff1, J L Stephenson, S A McLuckey.   

Abstract

The gas phase H/D exchange reactions of bradykinin (M + 3H)3+ ions with D2O and DI were monitored in a quadrupole ion trap mass spectrometer. The H/D exchange kinetics of both chemical probes (D2O and DI) indicate the presence of two noninterconverting reactive gas phase ion populations of bradykinin (M + 3H)3+ at room temperature. The H/D exchange involving DI, however, generally proceeds faster than that involving D2O. The rate observations described here can be rationalized on the basis of the "relay mechanism" (see Campbell et al. J. Am. Chem. Soc. 1995, 117, 12840-12854) recently proposed to account for H/D exchange between D2O and gaseous protonated polypeptides. The higher exchange rate with DI is believed to arise primarily as a result of its lower gas-phase acidity relative to that of D2O and, secondarily, as a result of the longer bond length of DI relative to that of OD in D2O.

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Year:  2000        PMID: 10689670     DOI: 10.1016/S1044-0305(99)00137-3

Source DB:  PubMed          Journal:  J Am Soc Mass Spectrom        ISSN: 1044-0305            Impact factor:   3.109


  16 in total

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  14 in total

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8.  Hydrogen-deuterium exchange at non-labile sites: a new reaction facet with broad implications for structural and dynamic determinations.

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10.  Cis-trans isomerizations of proline residues are key to bradykinin conformations.

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Journal:  J Am Chem Soc       Date:  2013-02-13       Impact factor: 15.419

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