
The Library
Mass spectrometry in demonstrating the site-specific nitration of hen egg white lysozyme by an improved electrochemical method
Tools
Matters, Dominic, Cooper, Helen J., McDonnell, Liam, Iniesta, Jesus, Heptinstall, John, Derrick, Peter J. , Walton, David and Peterson, Ian (2006) Mass spectrometry in demonstrating the site-specific nitration of hen egg white lysozyme by an improved electrochemical method. Analytical Biochemistry, Vol.356 (No.2). pp. 171-181. doi:10.1016/j.ab.2006.06.033 ISSN 0003-2697.
Research output not available from this repository.
Request-a-Copy directly from author or use local Library Get it For Me service.
Official URL: http://dx.doi.org/10.1016/j.ab.2006.06.033
Abstract
In producing a method for selective protein nitration, we previously demonstrated the electrochemical nitration of hen egg white lysozyme to be at Tyr23 initially, followed by bisnitration at Tyr20, but with no trisnitration at Tyr53. The nitration site was determined by sequencing a tryptic peptide that included Tyr23 and Tyr20, but possible effects on other regions of the protein were not determined. Moreover, the electrooxidation conditions were harsh, involving an oxidation potential of +1.2 V (vs. saturated calomel electrode [SCE]), no added nitrogen source except the lysozyme itself, and long reaction periods with copper flag electrodes. Here we report a gentler procedure using much shorter reaction times with nitrite as the nitration source, a lower potential (+0.85 V vs. SCE), and a platinum basket electrode. Intact protein analysis by electrospray Fourier transform ion cyclotron resonance mass spectrometry identified mono- and bisnitration products with mass increases of +45 and +90 Da, respectively, consistent with the substitution of NO2 for H. In addition, the results revealed that no other covalent change in the protein occurred following electrooxidation. Nozzle skimmer dissociation of the intact mononitrated species localized the modification site to Tyr20 or Tyr23. Matrix-assisted laser desorption/ ionization time-of-flight and electrospray ionization time-of-flight analysis of the tryptic peptides of mononitrated lysozyme identified the site of nitration as Tyr23. (c) 2006 Elsevier Inc. All rights reserved.
Item Type: | Journal Article | ||||
---|---|---|---|---|---|
Subjects: | Q Science > QD Chemistry | ||||
Divisions: | Faculty of Science, Engineering and Medicine > Science > Chemistry | ||||
Journal or Publication Title: | Analytical Biochemistry | ||||
Publisher: | Academic Press | ||||
ISSN: | 0003-2697 | ||||
Official Date: | 15 September 2006 | ||||
Dates: |
|
||||
Volume: | Vol.356 | ||||
Number: | No.2 | ||||
Number of Pages: | 11 | ||||
Page Range: | pp. 171-181 | ||||
DOI: | 10.1016/j.ab.2006.06.033 | ||||
Status: | Peer Reviewed | ||||
Publication Status: | Published | ||||
Access rights to Published version: | Restricted or Subscription Access |
Data sourced from Thomson Reuters' Web of Knowledge
Request changes or add full text files to a record
Repository staff actions (login required)
![]() |
View Item |