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research article

IR-induced conformational isomerization of a helical peptide in a cold ion trap

Seaiby, Caroline  
•
Zabuga, Aleksandra V.  
•
Svendsen, Annette
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2016
Journal of Chemical Physics

In this work we use laser-induced population transfer techniques to study the conformational isomerization of a helical peptide, Ac-Phe-(Ala)5-LysH+, in a cold ion trap. In one scheme, called IR-UV hole-filling spectroscopy, a single conformation is selectively excited with an IR pump laser via a distinct NH stretch vibration. After giving the vibrationally excited ions sufficient time to isomerize and re-cool in the trap, the new conformational redistribution is detected by UV photofragment spectroscopy. While we clearly observe a redistribution of the conformer populations due to isomerization, only those conformations that initially have population participate in this redistribution–we do not form conformers that were not initially present in the trap. In a second scheme, called IR-induced population transfer spectroscopy, we determine the fractional populations of the four stable conformations of Ac-Phe-(Ala)5-LysH+ by scanning the IR laser while selectively detecting a specific conformation using UV photofragment spectroscopy.

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Type
research article
DOI
10.1063/1.4939528
Web of Science ID

WOS:000368617300010

Author(s)
Seaiby, Caroline  
Zabuga, Aleksandra V.  
Svendsen, Annette
Rizzo, Thomas R.  
Date Issued

2016

Publisher

American Institute of Physics

Published in
Journal of Chemical Physics
Volume

144

Article Number

014304

Subjects

cryogenic ion spectroscopy

•

mass spectrometry

•

isomerization

•

peptides

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LCPM  
Available on Infoscience
January 5, 2016
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/122007
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