Molecular enzymology of carnitine transfer and transport

被引:323
作者
Ramsay, RR
Gandour, RD
van der Leij, FR
机构
[1] Univ St Andrews, Ctr Biomol Sci, St Andrews KY16 9ST, Fife, Scotland
[2] Virginia Polytech Inst & State Univ, Dept Chem, Blacksburg, VA 24061 USA
[3] Univ Groningen, Beatrix Childrens Hosp, Dept Pediat, NL-9700 RB Groningen, Netherlands
[4] Univ Groningen, Inst Drug Explorat, NL-9700 RB Groningen, Netherlands
来源
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEIN STRUCTURE AND MOLECULAR ENZYMOLOGY | 2001年 / 1546卷 / 01期
关键词
carnitine; OCTN2; CACT; carnitine acyltransferases; fatty acid oxidation; transport; molecular genetics; enzymology; inhibitor;
D O I
10.1016/S0167-4838(01)00147-9
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
Carnitine (L-3-hydroxy-4-N-trimethylaminobutyric acid) forms esters with a wide range of acyl groups and functions to transport and excrete these groups. It is found in most cells at millimolar levels after uptake via the sodium-dependent carrier, OCTN2. The acylation state of the mobile carnitine pool is linked to that of the limited and compartmentalised coenzyme A pools by the action of the family of carnitine acyltransferases and the mitochondrial membrane transporter, CACT. The genes and sequences of the carriers and the acyltransferases are reviewed along with mutations that affect activity. After summarising the accepted enzymatic background, recent molecular studies on the carnitine acyltransferases are described to provide a picture of the role and function of these freely reversible enzymes. The kinetic and chemical mechanisms are also discussed in relation to the different inhibitors under study for their potential to control diseases of lipid metabolism. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:21 / 43
页数:23
相关论文
共 209 条
[31]  
BURTON RM, 1953, J BIOL CHEM, V202, P873
[32]   Carnitine transporter OCTN2 mutations in systemic primary carnitine deficiency: A novel Arg169Gln mutation and a recurrent Arg282ter mutation associated with an unconventional splicing abnormality [J].
Burwinkel, B ;
Kreuder, J ;
Schweitzer, S ;
Vorgerd, M ;
Gempel, K ;
Gerbitz, KD ;
Kilimann, MW .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 261 (02) :484-487
[33]   Natural trans-splicing in carnitine octanoyltransferase pre-mRNAs in rat liver [J].
Caudevilla, C ;
Serra, D ;
Miliar, A ;
Codony, C ;
Asins, G ;
Bach, M ;
Hegardt, FG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (21) :12185-12190
[34]   SPECIFIC ALKYLATION OF A HISTIDINE RESIDUE IN CARNITINE ACETYLTRANSFERASE BY BROMOACETYL-L-CARNITINE [J].
CHASE, JFA ;
TUBBS, PK .
BIOCHEMICAL JOURNAL, 1970, 116 (04) :713-&
[35]   PH-DEPENDENCE OF CARNITINE ACETYLTRANSFERASE ACTIVITY [J].
CHASE, JFA .
BIOCHEMICAL JOURNAL, 1967, 104 (02) :503-&
[36]   SOME KINETIC STUDIES ON MECHANISM OF ACTION OF CARNITINE ACETYLTRANSFERASE [J].
CHASE, JFA ;
TUBBS, PK .
BIOCHEMICAL JOURNAL, 1966, 99 (01) :32-&
[37]   MOLECULAR-CLONING AND SEQUENCE-ANALYSIS OF THE RAT-LIVER CARNITINE OCTANOYLTRANSFERASE CDNA, ITS NATURAL GENE AND THE GENE PROMOTER [J].
CHOI, SJ ;
OH, DH ;
SONG, CS ;
ROY, AK ;
CHATTERJEE, B .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 1995, 1264 (02) :215-222
[38]   ACTIVE-TRANSPORT OF BUTYROBETAINE AND CARNITINE INTO ISOLATED LIVER-CELLS [J].
CHRISTIANSEN, RZ ;
BREMER, J .
BIOCHIMICA ET BIOPHYSICA ACTA, 1976, 448 (04) :562-577
[39]  
CHUNG CD, 1993, J BIOL CHEM, V268, P4519
[40]  
CLARKE PRH, 1981, J BIOL CHEM, V256, P9861