Document Detail


Post-translational modification in the gas phase: mechanism of cysteine S-nitrosylation via ion-molecule reactions.
MedLine Citation:
PMID:  22006383     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The gas-phase mechanism of S-nitrosylation of thiols was studied in a quadrupole ion trap mass spectrometer. This was done via ion-molecule reactions of protonated cysteine and many of its derivatives and other thiol ions with neutral tert-butyl nitrite or nitrous acid. Our results showed that the presence of the carboxylic acid functional group, -COOH, in the vicinity of the thiol group is essential for the gas-phase nitrosylation of thiols. When the carboxyl proton is replaced by a methyl group (cysteine methyl ester) no nitrosylation was observed. Other thiols lacking a carboxylic acid functional group displayed no S-nitrosylation, strongly suggesting that the carboxyl hydrogen plays a key role in the nitrosylation process. These results are in excellent agreement with a solution-phase mechanism proposed by Stamler et al. (J. S. Stamler, E. J. Toone, S. A. Lipton, N. J. Sucher. Neuron 1997, 18, 691-696) who suggested a catalytic role for the carboxylic acid group adjacent to cysteine residues and with later additions by Ascenzi et al. (P. Ascenzi, M. Colasanti, T. Persichini, M. Muolo, F. Polticelli, G. Venturini, D. Bordo, M. Bolognesi. Biol. Chem. 2000, 381, 623-627) who postulated that the presence of the carboxyl in the cysteine microenvironment in proteins is crucial for S-nitrosylation. A concerted mechanism for the gas-phase S-nitrosylation was proposed based on our results and was further studied using theoretical calculations. Our calculations showed that this proposed pathway is exothermic by 44.0 kJ mol(-1). This is one of the few recent examples when a gas-phase mechanism matches one in solution.
Authors:
Sandra Osburn; Richard A J O'Hair; Stephen M Black; Victor Ryzhov
Related Documents :
15827683 - Interactive effects of polyphenols, tocopherol and ascorbic acid on the cu2+-mediated o...
25239633 - Glycodeoxycholic acid levels as prognostic biomarker in acetaminophen-induced acute liv...
24469983 - The effect of o2 and co 2 concentration on photosynthesis and glycolate accumulation in...
Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Rapid communications in mass spectrometry : RCM     Volume:  25     ISSN:  1097-0231     ISO Abbreviation:  Rapid Commun. Mass Spectrom.     Publication Date:  2011 Nov 
Date Detail:
Created Date:  2011-10-18     Completed Date:  2012-01-03     Revised Date:  2014-02-04    
Medline Journal Info:
Nlm Unique ID:  8802365     Medline TA:  Rapid Commun Mass Spectrom     Country:  England    
Other Details:
Languages:  eng     Pagination:  3216-22     Citation Subset:  IM    
Copyright Information:
Copyright © 2011 John Wiley & Sons, Ltd.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Cysteine / analogs & derivatives*,  chemistry*
Mass Spectrometry
Models, Chemical
Nitrites / chemistry
Nitrosation
Nitrous Acid / chemistry
Protons
Thermodynamics
Grant Support
ID/Acronym/Agency:
HL067841/HL/NHLBI NIH HHS; HL60190/HL/NHLBI NIH HHS; R01 HL060190/HL/NHLBI NIH HHS; R01 HL067841/HL/NHLBI NIH HHS
Chemical
Reg. No./Substance:
0/Nitrites; 0/Protons; 44P8QG0F3T/n-butyl nitrite; K848JZ4886/Cysteine; RQ6L463N3B/mecysteine; T2I5UM75DN/Nitrous Acid
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  The use of strong anion-exchange (SAX) magnetic particles for the extraction of therapeutic siRNA an...
Next Document:  Graphene and graphene oxide: two ideal choices for the enrichment and ionization of long-chain fatty...