Efficiency of collisionally-activated dissociation and 193-nm photodissociation of peptide ions in fourier transform mass spectrometry

E R Williams; J J Furlong; F W McLafferty

doi:10.1016/1044-0305(90)85003-5

Efficiency of collisionally-activated dissociation and 193-nm photodissociation of peptide ions in fourier transform mass spectrometry

J Am Soc Mass Spectrom. 1990 Jul;1(4):288-94. doi: 10.1016/1044-0305(90)85003-5.

Authors

E R Williams¹, J J Furlong, F W McLafferty

Affiliation

¹ Chemistry Department, Baker Laboratory, Cornell University, 14853-1301, New York, Ithaca, USA.

PMID: 24248821
DOI: 10.1016/1044-0305(90)85003-5

Abstract

For tandem mass spectrometry, the Fourier transform instrument exhibits advantages for the use of collisionally-activated dissociation (CAD). The CAD energy deposited in larger ions can be greatly increased by extending the collision time to as much as 120 s, and the efficiency of trapping and measuring CAD product ions is many times greater than that found for triple-quadrupole or magnetic sector instruments, although the increased pressure from the collision gas is an offsetting disadvantage. A novel system that uses the same laser for photodesorption of ions and their subsequent photodissociation can produce complete dissociation of larger oligopeptide ions and unusually abundant fragment ions. In comparison to CAD, much more internal energy can be deposited in the primary ions using 193-nm photons, sufficient to dissociate peptide ions of m/z > 2000. Mass spectra closely resembling ion photodissociation spectra can also be obtained by' neutral photodissociation (193-nm laser irradiation of the sample) followed by ion photodesorption.