D-Amino acids in aged proteins: Analysis and biological relevance

被引:60
作者
Fujii, Noriko [1 ]
Kaji, Yuichi [2 ]
Fujii, Norihiko [1 ]
机构
[1] Kyoto Univ, Inst Res Reactor, Osaka 5900494, Japan
[2] Univ Tsukuba, Inst Clin Med, Dept Ophthalmol, Tsukuba, Ibaraki 3058575, Japan
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2011年 / 879卷 / 29期
关键词
D-Amino acid; D-Aspartate; Aging; Lens; Crystallin; Skin; Oxidative stress; CML; Racemization; Isomerization; UV B irradiation; ALPHA-A-CRYSTALLIN; BETA-ASPARTIC ACID; GLYCATION END-PRODUCTS; HUMAN LENS; MAILLARD REACTION; IMMUNOHISTOCHEMICAL LOCALIZATION; LIPID-PEROXIDATION; ALZHEIMERS-DISEASE; MARKED LONGEVITY; ELASTIC FIBERS;
D O I
10.1016/j.jchromb.2011.05.051
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Homochirality is essential for life. L-Amino acids are exclusively used as substrates for the polymerization and formation of peptides and proteins in living systems. However, D-amino acids, which are enantiomers of L-amino acids, were recently detected in various living organisms in the form of free D-amino acids and D-amino acid residues in peptides and proteins. In particular, D-aspartyl (Asp) residues have been detected in various proteins from diverse tissues of elderly individuals. Here, we describe three important aspects of our research: (i) a method for detecting D-beta-Asp at specific sites in particular proteins, (ii) a likely spontaneous mechanism by which Asp residues in proteins invert and isomerize to the D-beta-form with age under physiological conditions, (iii) a discussion of factors that favor such a reaction. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:3141 / 3147
页数:7
相关论文
共 47 条
[1]  
AHMED MU, 1986, J BIOL CHEM, V261, P4889
[2]   Protein crosslinking by the Maillard reaction: Dicarbonyl-derived imidazolium crosslinks in aging and diabetes [J].
Chellan, P ;
Nagaraj, RH .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1999, 368 (01) :98-104
[3]   Collagen fragments in urine derived from bone resorption are highly racemized and isomerized: a biological clock of protein aging with clinical potential [J].
Cloos, PAC ;
Fledelius, C .
BIOCHEMICAL JOURNAL, 2000, 345 :473-480
[4]   QUANTIFICATION OF D-ASPARTATE IN NORMAL AND ALZHEIMER BRAINS [J].
FISHER, GH ;
DANIELLO, A ;
VETERE, A ;
CUSANO, GP ;
CHAVEZ, M ;
PETRUCELLI, L .
NEUROSCIENCE LETTERS, 1992, 143 (1-2) :215-218
[5]   The advanced glycation end product, N-(epsilon)(carboxymethyl)lysine, is a product of both lipid peroxidation and glycoxidation reactions [J].
Fu, MX ;
Requena, JR ;
Jenkins, AJ ;
Lyons, TJ ;
Baynes, JW ;
Thorpe, SR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (17) :9982-9986
[6]   Age-related changes of alpha-crystallin aggregate in human lens [J].
Fujii, N. ;
Shimmyo, Y. ;
Sakai, M. ;
Sadakane, Y. ;
Nakamura, T. ;
Morimoto, Y. ;
Kinouchi, T. ;
Goto, Y. ;
Lampi, K. .
AMINO ACIDS, 2007, 32 (01) :87-94
[7]   D-amino acid formation induced by a chiral field within a human lens protein during aging [J].
Fujii, N ;
Harada, K ;
Momose, Y ;
Ishii, N ;
Akaboshi, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 263 (02) :322-326
[8]   Formation of four isomers at the Asp-151 residue of aged human αA-crystallin by natural aging [J].
Fujii, N ;
Takemoto, LJ ;
Momose, Y ;
Matsumoto, S ;
Hiroki, K ;
Akaboshi, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 265 (03) :746-751
[9]  
Fujii N, 2000, MOL VIS, V6, P1
[10]   SIMULTANEOUS STEREOINVERSION AND ISOMERIZATION AT SPECIFIC ASPARTIC-ACID RESIDUES IN ALPHA-A-CRYSTALLIN FROM HUMAN LENS [J].
FUJII, N ;
SATOH, K ;
HARADA, K ;
ISHIBASHI, Y .
JOURNAL OF BIOCHEMISTRY, 1994, 116 (03) :663-669