Proteomic analysis of age dependent nitration of rat cardiac proteins by solution isoelectric focusing coupled to nanoHPLC tandem mass spectrometry

被引:34
作者
Hong, Sung Jung [1 ]
Gokulrangan, Giridharan [1 ]
Schoneich, Christian [1 ]
机构
[1] Univ Kansas, Dept Pharmaceut Chem, Lawrence, KS 66047 USA
关键词
aging; heart; proteomics; 3-nitrotyrosine; mass spectrometry;
D O I
10.1016/j.exger.2007.03.005
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Protein nitration occurs as a result of oxidative stress induced by reactive oxygen (ROS) and reactive nitrogen species (RNS). Therefore, protein nitration serves as a hallmark for protein oxidation in vivo. We have previously reported on age dependent protein nitration in cardiac tissue of Fisher 344 BN-F1 rats analyzed by two-dimensional gel electrophoresis; however, only one specific nitration site was identified [Kanski, J., Behring, A., Pelling, J., Schoneich, C., 2005a. Proteomic identification of 3-nitrotyrosine-containing rat cardiac proteins: effects of biological aging. Am. J. Physiol. Heart Circ. Physiol. 288, H371-381]. In the present report, we used solution phase isoelectric focusing (IEF) followed by nanoHPLC-ESI-MS/MS that allowed us to obtain good MS/MS data to identify specific sites of protein nitration in cardiac tissue. As expected, more nitrated proteins were detected in cardiac tissue of old rats, including myosin heavy chain, neurofibromin, tropomyosin and nebulin-related anchoring protein. The post-translational modification of these cytoskeletal proteins may provide some rationale for the age-dependent functional decline of the heart. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:639 / 651
页数:13
相关论文
共 57 条
[1]   S-glutathiolation by peroxynitrite activates SERCA during arterial relaxation by nitric oxide [J].
Adachi, T ;
Weisbrod, RM ;
Pimentel, DR ;
Ying, J ;
Sharov, VS ;
Schöneich, C ;
Cohen, RA .
NATURE MEDICINE, 2004, 10 (11) :1200-1207
[2]   Molecular and cellular basis of the aetiology and management of diabetic cardiomyopathy: A short review [J].
Adeghate, E .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2004, 261 (1-2) :187-191
[3]   Cardiovascular proteomics - Tools to develop novel biomarkers and potential applications [J].
Arab, Sara ;
Gramolini, Anthony O. ;
Ping, Peipei ;
Kislinger, Thomas ;
Stanley, Brian ;
van Eyk, Jennifer ;
Ouzounian, Maral ;
MacLennan, David H. ;
Emili, Andrew ;
Liu, Peter P. .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2006, 48 (09) :1733-1741
[4]   Nitric oxide-dependent generation of reactive species in sickle cell disease - Actin tyrosine nitration induces defective cytoskeletal polymerization [J].
Aslan, M ;
Ryan, TM ;
Townes, TM ;
Coward, L ;
Kirk, MC ;
Barnes, S ;
Alexander, CB ;
Rosenfeld, SS ;
Freeman, BA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (06) :4194-4204
[5]   CONTROL OF CARDIAC-MUSCLE CELL-FUNCTION BY AN ENDOGENOUS NITRIC-OXIDE SIGNALING SYSTEM [J].
BALLIGAND, JL ;
KELLY, RA ;
MARSDEN, PA ;
SMITH, TW ;
MICHEL, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (01) :347-351
[6]   Oxidative damage and tyrosine nitration from peroxynitrite [J].
Beckman, JS .
CHEMICAL RESEARCH IN TOXICOLOGY, 1996, 9 (05) :836-844
[7]   KINETICS OF SUPEROXIDE DISMUTASE-CATALYZED AND IRON-CATALYZED NITRATION OF PHENOLICS BY PEROXYNITRITE [J].
BECKMAN, JS ;
ISCHIROPOULOS, H ;
ZHU, L ;
VANDERWOERD, M ;
SMITH, C ;
CHEN, J ;
HARRISON, J ;
MARTIN, JC ;
TSAI, M .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1992, 298 (02) :438-445
[8]   Congenital myopathies: diseases of the actin cytoskeleton [J].
Clarkson, E ;
Costa, CF ;
Machesky, LM .
JOURNAL OF PATHOLOGY, 2004, 204 (04) :407-417
[9]   Proteasome inactivation upon aging and on oxidation-effect of HSP 90 [J].
Conconi, M ;
Friguet, B .
MOLECULAR BIOLOGY REPORTS, 1997, 24 (1-2) :45-50
[10]   Effects of NO on mitochondrial function in cardiomyocytes: Pathophysiological relevance [J].
Davidson, Sean M. ;
Duchen, Michael R. .
CARDIOVASCULAR RESEARCH, 2006, 71 (01) :10-21