Literature DB >> 15133838

Mass spectrometry for detection of 4-hydroxy-trans-2-nonenal (HNE) adducts with peptides and proteins.

Marina Carini1, Giancarlo Aldini, Roberto Maffei Facino.   

Abstract

Despite the great technical advancement of mass spectrometry, this technique has contributed in a limited way to the discovery and quantitation of specific/precocious markers linked to free radical-mediated diseases. Unsaturated aldehydes generated by free radical-induced lipid peroxidation of polyunsaturated fatty acids, and in particular 4-hydroxy-trans-2 nonenal (HNE), are involved in the onset and progression of many pathologies such as cardiovascular (atherosclerosis, long-term complications of diabetes) and neurodegenerative diseases (Alzheimer's disease, Parkinson's disease, and cerebral ischemia). Most of the biological effects of HNE are attributed to the capacity of HNE to react with the nucleophilic sites of proteins and peptides (other than nucleic acids), to form covalently modified biomolecules that can disrupt important cellular functions and induce mutations. By considering the emerging role of HNE in several human diseases, an unequivocal analytical approach as mass spectrometry to detect/elucidate the structure of protein-HNE adducts in biological matrices is strictly needed not only to understand the reaction mechanism of HNE, but also to gain a deeper insight into the pathological role of HNE. This with the aim to provide intermediate diagnostic biomarkers for human diseases. This review sheds focus on the "state-of-the-art" of mass spectrometric applications in the field of HNE-protein adducts characterization, starting from the fundamental early studies and discussing the different MS-based approaches that can provide detailed information on the mechanistic aspects of HNE-protein interaction. In the last decade, the increases in the accessible mass ranges of modern instruments and advances in ionization methods have made possible a fundamental improvement in the analysis of protein-HNE adducts by mass spectrometry, and in particular by matrix-assisted laser desorption/ionization (MALDI) and electrospray ionization (ESI) tandem mass spectrometry. The recent developments and uses of combined analytical approaches to detect and characterize the type/site of interaction have been highlighted, and several other aspects, including sample preparation methodologies, structure elucidation, and data analysis have also been considered. Copyright 2004 Wiley Periodicals, Inc., Mass Spec Rev 23:281-305, 2004

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Year:  2004        PMID: 15133838     DOI: 10.1002/mas.10076

Source DB:  PubMed          Journal:  Mass Spectrom Rev        ISSN: 0277-7037            Impact factor:   10.946


  55 in total

1.  The reactivity of human serum albumin toward trans-4-hydroxy-2-nonenal.

Authors:  Qingyuan Liu; David C Simpson; Scott Gronert
Journal:  J Mass Spectrom       Date:  2012-04       Impact factor: 1.982

2.  Glutathione transferase A4-4 resists adduction by 4-hydroxynonenal.

Authors:  Laura M Shireman; Kimberly A Kripps; Larissa M Balogh; Kip P Conner; Dale Whittington; William M Atkins
Journal:  Arch Biochem Biophys       Date:  2010-09-15       Impact factor: 4.013

3.  Targeted 18O-labeling for improved proteomic analysis of carbonylated peptides by mass spectrometry.

Authors:  Mikel R Roe; Thomas F McGowan; LaDora V Thompson; Timothy J Griffin
Journal:  J Am Soc Mass Spectrom       Date:  2010-03-29       Impact factor: 3.109

4.  Utilization of LC-MS/MS analyses to identify site-specific chemical protein adducts in vitro.

Authors:  Ashley A Fisher; Matthew T Labenski; Terrence J Monks; Serrine S Lau
Journal:  Methods Mol Biol       Date:  2011

5.  Membrane-mediated amyloidogenesis and the promotion of oxidative lipid damage by amyloid beta proteins.

Authors:  Ian V J Murray; Liu Liu; Hiroaki Komatsu; Kunihiro Uryu; Gang Xiao; John A Lawson; Paul H Axelsen
Journal:  J Biol Chem       Date:  2007-01-24       Impact factor: 5.157

6.  Formation of 4-hydroxynonenal from cardiolipin oxidation: Intramolecular peroxyl radical addition and decomposition.

Authors:  Wei Liu; Ned A Porter; Claus Schneider; Alan R Brash; Huiyong Yin
Journal:  Free Radic Biol Med       Date:  2010-11-01       Impact factor: 7.376

Review 7.  Analysis of endogenous glutathione-adducts and their metabolites.

Authors:  Ian A Blair
Journal:  Biomed Chromatogr       Date:  2010-01       Impact factor: 1.902

8.  Substrate specificity combined with stereopromiscuity in glutathione transferase A4-4-dependent metabolism of 4-hydroxynonenal.

Authors:  Larissa M Balogh; Isolde Le Trong; Kimberly A Kripps; Laura M Shireman; Ronald E Stenkamp; Wei Zhang; Bengt Mannervik; William M Atkins
Journal:  Biochemistry       Date:  2010-02-23       Impact factor: 3.162

9.  A comparative 'bottom up' proteomics strategy for the site-specific identification and quantification of protein modifications by electrophilic lipids.

Authors:  Bingnan Han; Michael Hare; Samanthi Wickramasekara; Yi Fang; Claudia S Maier
Journal:  J Proteomics       Date:  2012-07-26       Impact factor: 4.044

10.  Charge-derivatized amino acids facilitate model studies on protein side-chain modifications by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.

Authors:  Xiaochun Zhu; Vernon E Anderson; Lawrence M Sayre
Journal:  Rapid Commun Mass Spectrom       Date:  2009-07       Impact factor: 2.419

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