Mammalian transglutaminases - Identification of substrates as a key to physiological function and physiopathological relevance

被引:153
|
作者
Esposito, C [1 ]
Caputo, I [1 ]
机构
[1] Univ Salerno, Dept Chem, I-84081 Baronissi, Italy
关键词
post-translational modification; protein substrates; proteomics; transglutaminase;
D O I
10.1111/j.1742-4658.2004.04476.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Transglutaminases form a large family of intracellular and extracellular enzymes that catalyse the Ca2+-dependent post-translational modification of proteins. Despite significant advances in our understanding of the biological role of most mammalian transglutaminase isoforms, recent findings suggest new scenarios, most notably for the ubiquitous tissue transglutaminase. It is becoming apparent that some transglutaminases, normally expressed at low levels in many tissue types, are activated and/or overexpressed in a variety of diseases, thereby resulting in enhanced concentrations of cross-linked proteins. As applies to all enzymes that exert their metabolic function by modifying the properties of target proteins, the identification and characterization of the modified proteins will cast light on the functions of transglutaminases and their involvement in human diseases. In this paper we review data on the properties of mammalian transglutaminases, particularly as regards their protein substrates and the relevance of transglutaminase-catalysed reactions in physiological and disease conditions.
引用
收藏
页码:615 / 631
页数:17
相关论文
共 50 条
  • [21] NA+, K+-ATPASE AND NA+/CA2+ EXCHANGE ISOFORMS - PHYSIOLOGICAL AND PHYSIOPATHOLOGICAL RELEVANCE
    DECOLLOGNE, S
    BERTRAND, IB
    ASCENSIO, M
    DRUBAIX, I
    LELIEVRE, LG
    JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1993, 22 : S96 - S98
  • [22] UPTAKE OF PURINE SUBSTRATES SHOWS MAJOR PHYSIOLOGICAL VARIATIONS IN MAMMALIAN SKIN FIBROBLASTS
    BAUMGARTEN, I
    HARLEY, EH
    COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY B-BIOCHEMISTRY & MOLECULAR BIOLOGY, 1995, 110 (01): : 37 - 46
  • [23] STRUCTURE AND BINDING OF UNCONJUGATED BILIRUBIN - RELEVANCE FOR PHYSIOLOGICAL AND PATHOPHYSIOLOGICAL FUNCTION
    OSTROW, JD
    MUKERJEE, P
    TIRIBELLI, C
    JOURNAL OF LIPID RESEARCH, 1994, 35 (10) : 1715 - 1737
  • [24] Key individual identification using dimensional relevance in the stratum of networks
    Noor, Fozia
    Akram, Muhammad Usman
    Shah, Asadullah
    Khan, Shoab Ahmad
    JOURNAL OF INTELLIGENT & FUZZY SYSTEMS, 2019, 37 (02) : 2153 - 2167
  • [25] Force-frequency relationship in intact mammalian ventricular myocardium: physiological and pathophysiological relevance
    Endoh, M
    EUROPEAN JOURNAL OF PHARMACOLOGY, 2004, 500 (1-3) : 73 - 86
  • [26] Identification and physiological function of a yeast NADPH oxidase
    Breitenbach, M.
    Rinnerthaler, M.
    Heeren, G.
    Laun, P.
    Koessler, S.
    Rid, R.
    Klinger, H.
    FREE RADICAL RESEARCH, 2008, 42 : S44 - S44
  • [27] Inhibition of Mammalian Glycoprotein YKL-40 IDENTIFICATION OF THE PHYSIOLOGICAL LIGAND
    Kognole, Abhishek A.
    Payne, Christina M.
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2017, 292 (07) : 2624 - 2636
  • [28] Identification of the Endogenous Key Substrates of the Human Organic Cation Transporter OCT2 and Their Implication in Function of Dopaminergic Neurons
    Taubert, Dirk
    Grimberg, Gundula
    Stenzel, Werner
    Schoemig, Edgar
    PLOS ONE, 2007, 2 (04):
  • [29] Global identification and analysis of isozyme-specific possible substrates crosslinked by transglutaminases using substrate peptides in mouse liver fibrosis
    Tatsukawa, Hideki
    Tani, Yuji
    Otsu, Risa
    Nakagawa, Haruka
    Hitomi, Kiyotaka
    SCIENTIFIC REPORTS, 2017, 7
  • [30] Global identification and analysis of isozyme-specific possible substrates crosslinked by transglutaminases using substrate peptides in mouse liver fibrosis
    Hideki Tatsukawa
    Yuji Tani
    Risa Otsu
    Haruka Nakagawa
    Kiyotaka Hitomi
    Scientific Reports, 7