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PMID: 18683952 Published · ppublish English Journal Article Research Support, N.I.H., Extramural

Reactive-electrospray-assisted laser desorption/ionization for characterization of peptides and proteins.

Analytical chemistry ·Vol. 80 ·No. 18 ·2008-09-15 ·Pages 6995-7003

Peng IX, Ogorzalek Loo RR, Shiea J, Loo JA

Abstract

Electrospray-assisted laser desorption/ionization (ELDI) is a soft ionization method for mass spectrometry (MS) and combines features of both electrospray ionization (ESI) and matrix-assisted laser desorption/ionization to generate ESI-like multiply charged molecules. The ELDI process is based on merging ESI-generated, charged droplets with particles UV laser desorbed from dried or wet sample deposits. We previously reported that ELDI is amenable for MS-based protein identification of large peptides and small proteins using top-down and bottom-up techniques (Peng, I. X.; Shiea, J.; Ogorzalek Loo, R. R.; Loo, J. A. Rapid Commun. Mass Spectrom. 2007, 21, 2541-2546). We have extended our studies by applying collisionally activated dissociation and electron-transfer dissociation MS ( n ) to protein analysis and show that ELDI is capable of multistage MS to MS (4) for top-down characterization of large proteins such as 29 kDa carbonic anhydrase. Multiply charged proteins generated by the ELDI mechanism can be shifted to higher charge by increasing the organic content in the ESI solvent to denature the protein molecules, or by adding m-nitrobenzyl alcohol to the ESI solvent. Furthermore, we introduce "reactive-ELDI", which supports chemical reactions during the ELDI process. Preliminary data for online disulfide bond reduction using dithiothreitol on oxidized glutathione and insulin show reactive-ELDI to be effective. These data provide evidence that the laser-desorbed particles merge with the ESI-generated charge droplets to effect chemical reactions prior to online MS detection. This capability should allow other chemical and enzymatic reactions to be exploited as online protein characterization tools, as well as extending them to flexible, spatially resolved tissue screening and imaging. Also, these reactive-ELDI disulfide reduction experiments enable direct top-down protein identification for proteomic study, side stepping laborious, time-consuming sample preparation steps such as in-solution reduction and alkylation.

MeSH Terms
Amino Acid Sequence Animals Cattle Disulfides/chemistry Dithiothreitol/metabolism Electron Transport Gases/chemistry Glutathione/metabolism Insulin/metabolism Molecular Weight Organic Chemicals/chemistry Peptides/analysis,chemistry,metabolism Protein Conformation Proteins/analysis,chemistry,metabolism Sequence Analysis, Protein Solvents/chemistry Spectrometry, Mass, Electrospray Ionization/methods Tandem Mass Spectrometry
Chemicals
Disulfides Gases Insulin Organic Chemicals Peptides Proteins Solvents Glutathione Dithiothreitol
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Peng Ivory X
Department of Chemistry and Biochemistry, University of California-Los Angeles, Los Angeles, California 90095, USA.
Ogorzalek Loo Rachel R
Shiea Jentaie
Loo Joseph A
Article Info
Journal
Analytical chemistry
Abbr.
Anal Chem
ISSN
1520-6882
Published
2008-09-15
Epub
2008-00-07
Pages
6995-7003
Language
English
Region
United States
NLM ID
0370536
Subset
IM
Grants
NCI NIH HHS · R21CA126106 · United States
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