Rapidly switchable matrix-assisted laser desorption/ionization and electrospray quadrupole-time-of-flight mass spectrometry for protein identification

被引:104
作者
Krutchinsky, AN [1 ]
Zhang, WZ [1 ]
Chait, BT [1 ]
机构
[1] Rockefeller Univ, New York, NY 10021 USA
关键词
D O I
10.1016/S1044-0305(00)00114-8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We describe a new interface for a prototype quadrupole-quadrupole-time-of-flight (TOF) mass spectrometer (Centaur, Sciex) that allows rapid switching between electrospray ionization (ESI) and matrix-assisted laser desorption/ionization (MALDI) modes of operation. Instrument performance in both modes is comparable (i.e., resolution similar to 10,000 FWHM, mass accuracy <10 ppm, sensitivity similar to 1 fmol) because the ion source is decoupled from the TOF mass analyzer by extensive gas collisions in the quadrupole stages of the instrument. The capacity to obtain side-by-side high quality ESI and MALDI mass spectra from a single proteolytic mixture greatly facilitates the identification of proteins and elucidation of their primary structures. Improved strategies for protein identification result from this ability to measure spectra using both ionization modes in the same instrument and to perform MS/MS on singly charged as well as multiply charged ions. Examples are provided to demonstrate the utility and performance of the modified instrument. (J Am Soc Mass Spectrom 2000, 11, 493-504) (C) 2000 American Society for Mass Spectrometry.
引用
收藏
页码:493 / 504
页数:12
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