Bioelectronome. integrated approach to receptor chemistry, radicals, electrochemistry, cell signaling, and physiological effects based on electron transfer

被引:16
作者
Kovacic, Peter [1 ]
Pozos, Robert S.
机构
[1] San Diego State Univ, Dept Chem, San Diego, CA 92128 USA
[2] San Diego State Univ, Dept Biol, San Diego, CA 92182 USA
关键词
receptor; electron transfer; radicals; cell signaling; bioelectrochemistry; mechanism; bioelectronome; 5,6-DIMETHYLXANTHENONE-4-ACETIC ACID DMXAA; GROWTH-FACTOR-RECEPTOR; C INDUCES APOPTOSIS; NF-KAPPA-B; OXIDATIVE STRESS; MITOMYCIN-C; HYDROGEN-PEROXIDE; ESTROGEN-RECEPTOR; DNA-ADDUCTS; POLYCHLORINATED-BIPHENYLS;
D O I
10.1080/10799890701509133
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
Bioelectronome refers to the host of electron transfer (ET) reactions that occur in living systems. This review presents an integrated approach to receptor chemistry based on electron transfer, radicals, electrochemistry, cell signaling, and end result. First, receptor activity is addressed from the unifying standpoint of redox transformations in which various receptors are discussed. After a listing of receptor-binding modes, receptor chemistry is treated with focus on generation of reactive oxygen species (ROS), activation by ROS, and subsequent cell signaling involving ROS. A general electrostatic mechanism is proposed for receptor-ligand action with supporting evidence. Cell-signaling processes appear to entail electron transfer, ROS, redox chains, and relays. The widespread involvement of phosphate from phosphorylation may be rationalized electrostatically by analogy with DNA phosphate.. Extensive evidence supports important participation of ET functionalities in the mechanism of drugs and toxins. The integrated approach is applied to the main ET classes, namely, quinones, metal complexes, iminium species, and aromatic nitro compounds.
引用
收藏
页码:261 / 294
页数:34
相关论文
共 147 条
[1]   Estrogen-nucleic acid adducts: Dissection of the reaction of 3,4-estrone quinone and its radical anion and radical cation with deoxynucleosides and DNA [J].
Akanni, A ;
Abul-Hajj, YJ .
CHEMICAL RESEARCH IN TOXICOLOGY, 1999, 12 (12) :1247-1253
[2]   c-Myc-dependent etoposide-induced apoptosis involves activation of Bax and caspases, and PKCdelta signaling [J].
Albihn, Ami ;
Loven, Jakob ;
Ohlsson, Johan ;
Osorio, Lyda M. ;
Henriksson, Marie .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2006, 98 (06) :1597-1614
[3]   Hydrogen peroxide causes uncoupling of dopamine D1-like receptors from G proteins via a mechanism involving protein kinase C and G-protein-coupled receptor kinase 2 [J].
Asghar, M ;
Banday, AA ;
Fardoun, RZ ;
Lokhandwala, MF .
FREE RADICAL BIOLOGY AND MEDICINE, 2006, 40 (01) :13-20
[4]   Mechanisms of action of DNA intercalating acridine-based drugs: How important are contributions from electron transfer and oxidative stress? [J].
Baguley, BC ;
Wakelin, LPG ;
Jacintho, JD ;
Kovacic, P .
CURRENT MEDICINAL CHEMISTRY, 2003, 10 (24) :2643-2649
[5]  
BAGULEY BC, 2001, CURR OPIN INVEST DR, V2, P267
[6]   Reactive oxygen species stimulates receptor activator of NF-κB ligand expression in osteoblast [J].
Bai, XC ;
Lu, D ;
Liu, AL ;
Zhang, ZM ;
Li, XM ;
Zou, ZP ;
Zeng, WS ;
Cheng, BL ;
Luo, SQ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (17) :17497-17506
[7]   Ontogenetic alterations in prototypical transcription factors in the rat cerebellum and hippocampus following perinatal exposure to a commercial PCB mixture [J].
Basha, MR ;
Braddy, NS ;
Zawia, NH ;
Kodavanti, PRS .
NEUROTOXICOLOGY, 2006, 27 (01) :118-124
[8]   NEUTRAL AND CHARGED BIRADICALS, ZWITTERIONS, FUNNELS IN S1, AND PROTON TRANSLOCATION - THEIR ROLE IN PHOTOCHEMISTRY, PHOTOPHYSICS, AND VISION [J].
BONACICKOUTECKY, V ;
KOUTECKY, J ;
MICHL, J .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 1987, 26 (03) :170-189
[9]   Peroxide-inducible Ets-1 mediates platelet-derived growth factor receptor-α gene transcription in vascular smooth muscle cells [J].
Bonello, MR ;
Bobryshev, YV ;
Khachigian, LM .
AMERICAN JOURNAL OF PATHOLOGY, 2005, 167 (04) :1149-1159
[10]  
Bowles MR, 1997, J BIOCHEM-TOKYO, V122, P101, DOI 10.1093/oxfordjournals.jbchem.a021716