The enzymology of the human prostanoid pathway

被引:11
作者
Biringer, Roger Gregory [1 ]
机构
[1] Lake Erie Coll Osteopath Med, Coll Osteopath Med, Bradenton, FL 34211 USA
关键词
Prostaglandin; Prostanoid; Thromboxane; Prostacyclin; Kinetics; Enzymology; PROSTAGLANDIN-D SYNTHASE; TISSUE-SPECIFIC EXPRESSION; THROMBOXANE SYNTHASE; PROSTACYCLIN SYNTHASE; CATALYTIC MECHANISM; CEREBROSPINAL-FLUID; CRYSTAL-STRUCTURE; STRUCTURAL BASIS; E-2; SYNTHASE; F SYNTHASE;
D O I
10.1007/s11033-020-05526-z
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
Prostanoids are short-lived autocrine and paracrine signaling molecules involved in a wide range of biological functions. They have been shown to be intimately involved in many different disease states when their regulation becomes dysfunctional. In order to fully understand the progression of any disease state or the biological functions of the well state, a complete evaluation of the genomics, proteomics, and metabolomics of the system is necessary. This review is focused on the enzymology for the enzymes involved in the synthesis of the prostanoids (prostaglandins, prostacyclins and thromboxanes). In particular, the isolation and purification of the enzymes, their enzymatic parameters and catalytic mechanisms are presented.
引用
收藏
页码:4569 / 4586
页数:18
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