Control of oxygenation in lipoxygenase and cyclooxygenase catalysis

被引:244
作者
Schneider, Claus
Pratt, Derek A.
Porter, Ned A.
Brash, Alan R.
机构
[1] Vanderbilt Univ, Dept Pharmacol, Nashville, TN 37232 USA
[2] Vanderbilt Univ, Dept Chem, Nashville, TN 37232 USA
[3] Vanderbilt Univ, Vanderbilt Inst Chem Biol, Nashville, TN 37232 USA
[4] Queens Univ, Dept Chem, Kingston, ON K7L 3N6, Canada
来源
CHEMISTRY & BIOLOGY | 2007年 / 14卷 / 05期
关键词
D O I
10.1016/j.chembiol.2007.04.007
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
Lipoxygenases (LOX) and cyclooxygenases (COX) react an achiral polyunsaturated fatty acid with oxygen to form a chiral peroxide product of high regio- and stereochemical purity. Both enzymes employ free radical chemistry reminiscent of hydrocarbon autoxidation but execute efficient control during catalysis to form a specific product over the multitude of isomers found in the nonenzymatic reaction. Exactly how both dioxygenases achieve this positional and stereos control is far from clear. We present four mechanistic models, not mutually exclusive, that could account for the specific reactions of molecular oxygen with a fatty acid in the LOX or COX active site.
引用
收藏
页码:473 / 488
页数:16
相关论文
共 105 条
[71]   Mechanism of free radical oxygenation of polyunsaturated fatty acids by cyclooxygenases [J].
Rouzer, CA ;
Marnett, LJ .
CHEMICAL REVIEWS, 2003, 103 (06) :2239-2304
[72]   Spatial requirements for 15-(R)-hydroxy-5Z,8Z,11Z,13E-eicosatetraenoic acid synthesis within the cyclooxygenase active site of murine COX-2 -: Why acetylated COX-1 does not synthesize 15-(R)-HETE [J].
Rowlinson, SW ;
Crews, BC ;
Goodwin, DC ;
Schneider, C ;
Gierse, JK ;
Marnett, LJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (09) :6586-6591
[73]   X-RAY SPECTROSCOPY OF THE IRON SITE IN SOYBEAN LIPOXYGENASE-1 - CHANGES IN COORDINATION UPON OXIDATION OR ADDITION OF METHANOL [J].
SCARROW, RC ;
TRIMITSIS, MG ;
BUCK, CP ;
GROVE, GN ;
COWLING, RA ;
NELSON, MJ .
BIOCHEMISTRY, 1994, 33 (50) :15023-15035
[74]   EFFECT OF LIPID HYDROPEROXIDE ON LIPOXYGENASE KINETICS [J].
SCHILSTRA, MJ ;
VELDINK, GA ;
VERHAGEN, J ;
VLIEGENTHART, JFG .
BIOCHEMISTRY, 1992, 31 (33) :7692-7699
[75]   Identification of two cyclooxygenase active site residues, leucine 384 and glycine 526, that control carbon ring cyclization in prostaglandin biosynthesis [J].
Schneider, C ;
Boeglin, WE ;
Brash, AR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (06) :4404-4414
[76]   Stereospecificity of hydrogen abstraction in the conversion of arachidonic acid to 15R-HETE by aspirin-treated cyclooxygenase-2 -: Implications for the alignment of substrate in the active site [J].
Schneider, C ;
Brash, AR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (07) :4743-4746
[77]   Lipoxygenase-catalyzed formation of R-configuration hydroperoxides [J].
Schneider, C ;
Brash, AR .
PROSTAGLANDINS & OTHER LIPID MEDIATORS, 2002, 68-9 :291-301
[78]   Control of prostaglandin stereochemistry at the 15-carbon by cyclooxygenases-1 and -2 - A critical role for serine 530 and valine 349 [J].
Schneider, C ;
Boeglin, WE ;
Prusakiewicz, JJ ;
Rowlinson, SW ;
Marnett, LJ ;
Samel, N ;
Brash, AR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (01) :478-485
[79]   Enzymatic transition states and transition state analogues [J].
Schramm, VL .
CURRENT OPINION IN STRUCTURAL BIOLOGY, 2005, 15 (06) :604-613
[80]   ESR-SPECTRUM OF A PERPENDICULAR BENZYL RADICAL [J].
SCHREINER, K ;
BERNDT, A .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 1974, 13 (02) :144-145