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多个步骤决定了人3型3α-羟基类固醇脱氢酶催化5α-二氢睾酮还原的总体速率:对雄激素消除的影响。

Multiple steps determine the overall rate of the reduction of 5alpha-dihydrotestosterone catalyzed by human type 3 3alpha-hydroxysteroid dehydrogenase: implications for the elimination of androgens.

作者信息

Jin Yi, Penning Trevor M

机构信息

Center of Excellence in Environmental Toxicology, Department of Pharmacology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104-6084, USA.

出版信息

Biochemistry. 2006 Oct 31;45(43):13054-63. doi: 10.1021/bi060591r.

Abstract

Human type 3 3alpha-hydroxysteroid dehydrogenase, or aldo-keto reductase (AKR) 1C2, eliminates the androgen signal in human prostate by reducing 5alpha-dihydrotestosterone (DHT, potent androgen) to form 3alpha-androstanediol (inactive androgen), thereby depriving the androgen receptor of its ligand. The k(cat) for the NADPH-dependent reduction of DHT catalyzed by AKR1C2 is 0.033 s(-1). We employed transient kinetics and kinetic isotope effects to dissect the contribution of discrete steps to this low k(cat) value. Stopped-flow experiments to measure the formation of the AKR1C2.NADP(H) binary complex indicated that two slow isomerization events occur to yield a tight complex. A small primary deuterium isotope effect on k(cat) (1.5) and a slightly larger effect on k(cat)/K(m) (2.1) were observed in the steady state. In the transient state, the maximum rate constant for the single turnover of DHT (k(trans)) was determined to be 0.11 s(-1) for the NADPH-dependent reaction, which was approximately 4-fold greater than the corresponding k(cat) x k(trans) was significantly reduced when NADPD was substituted for NADPH, resulting in an apparent (D)k(trans) of 3.5. Thus, the effects of isotopic substitution on the hydride transfer step were masked by slow events that follow or precede the chemical transformation. Transient multiple-turnover reactions generated curvilinear reaction traces, consistent with the product formation and release occurring at comparable rates. Global fitting analysis of the transient kinetic data enabled the estimate of the rate constants for the three-step cofactor binding/release model and for the minimal ordered bi-bi turnover mechanism. Results were consistent with a kinetic mechanism in which a series of slow events, including the chemical step (0.12 s(-1)), the release of the steroid product (0.081 s(-1)), and the release of the cofactor product (0.21 s(-1)), combine to yield the overall observed low turnover number.

摘要

人3型3α-羟基类固醇脱氢酶,即醛酮还原酶(AKR)1C2,通过将5α-二氢睾酮(DHT,强效雄激素)还原形成3α-雄烷二醇(无活性雄激素)来消除人前列腺中的雄激素信号,从而使雄激素受体失去其配体。AKR1C2催化的NADPH依赖性还原DHT的催化常数(k(cat))为0.033 s(-1)。我们采用瞬态动力学和动力学同位素效应来剖析各个步骤对这个低k(cat)值的贡献。用于测量AKR1C2.NADP(H)二元复合物形成的停流实验表明,发生了两个缓慢的异构化事件以产生紧密复合物。在稳态下观察到对k(cat)有小的一级氘同位素效应(1.5),对k(cat)/K(m)有稍大的效应(2.1)。在瞬态下,对于NADPH依赖性反应,DHT单周转的最大速率常数(k(trans))被确定为0.11 s(-1),这大约是相应k(cat)的4倍当用NADPD替代NADPH时,k(trans)显著降低,导致表观(D)k(trans)为3.5。因此,同位素取代对氢化物转移步骤的影响被化学转化之前或之后的缓慢事件所掩盖。瞬态多周转反应产生曲线形反应轨迹,这与产物形成和释放以相当的速率发生一致。对瞬态动力学数据的全局拟合分析能够估计三步辅因子结合/释放模型和最小有序双底物双产物周转机制的速率常数。结果与一种动力学机制一致,在该机制中,一系列缓慢事件,包括化学步骤(0.12 s(-1))、类固醇产物的释放(0.081 s(-1))和辅因子产物的释放(0.21 s(-1)),共同导致总体观察到的低周转数。

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本文引用的文献

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Aldo-keto reductase (AKR) 1C3: role in prostate disease and the development of specific inhibitors.
Mol Cell Endocrinol. 2006 Mar 27;248(1-2):182-91. doi: 10.1016/j.mce.2005.12.009. Epub 2006 Jan 18.
3
The roles of aldo-keto reductases in steroid hormone action.
Drug News Perspect. 2004 Nov;17(9):563-78. doi: 10.1358/dnp.2004.17.9.872570.
7
Structure-function of human 3 alpha-hydroxysteroid dehydrogenases: genes and proteins.
Mol Cell Endocrinol. 2004 Feb 27;215(1-2):63-72. doi: 10.1016/j.mce.2003.11.006.
8
Crystal structure of human prostaglandin F synthase (AKR1C3).
Biochemistry. 2004 Mar 2;43(8):2188-98. doi: 10.1021/bi036046x.
10
Structure-function relationships in 3alpha-hydroxysteroid dehydrogenases: a comparison of the rat and human isoforms.
J Steroid Biochem Mol Biol. 2003 Jun;85(2-5):247-55. doi: 10.1016/s0960-0760(03)00236-x.

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