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二环己基碳二亚胺对(钠,钾)-ATP酶的抑制作用。酶活性所必需的两个羧基的证据。

Inhibition of (Na+,K+)-ATPase by dicyclohexylcarbodiimide. Evidence for two carboxyl groups that are essential for enzymatic activity.

作者信息

Gorga F R

出版信息

Biochemistry. 1985 Nov 19;24(24):6783-8. doi: 10.1021/bi00345a009.

Abstract

N,N'-Dicyclohexylcarbodiimide (DCCD), a reagent that reacts with carboxyl groups under mild conditions, irreversibly inhibits (Na+,K+)-ATPase activity (measured by using 1 mM ATP) with a pseudo-first-order rate constant of 0.084 min-1 (0.25 mM DCCD and 37 degrees C). The partial activities of the enzyme, including (Na+,K+)-ATPase at 1 microM ATP, Na+-ATPase, and the formation of enzyme-acyl phosphate (E-P), decayed at about one-third the rate at which (Na+,K+)-ATPase at 1 mM ATP was lost. The formation of E-P from inorganic phosphate was unaffected by DCCD while K+-phosphatase activity decayed at the same rate as (Na+,K+)-ATPase measured at 1 mM ATP. The enzyme's substrates (i.e., sodium, potassium, magnesium, and ATP) all decreased the rate of DCCD inactivation of (Na+,K+)-ATPase activity measured at either 1 mM or 1 microM ATP. The concentration dependence of the protection afforded by each substrate is consistent with its binding at a catalytically relevant site. DCCD also causes cross-linking of the enzyme into species of very high molecular weight. This process occurs at about one-tenth the rate at which (Na+,K+)-ATPase activity measured at 1 mM ATP is lost, too slowly to be related to the loss of enzymatic activity. Labeling of the enzyme with [14C]DCCD shows the incorporation of approximately 1 mol of DCCD per mole of large subunit; however, the incorporation is independent of the loss of enzymatic activity. The results presented here suggest that (Na+,K+)-ATPase contains two carboxyl groups that are essential for catalytic activity, in addition to the previously known aspartate residue which is involved in formation of E-P.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

N,N'-二环己基碳二亚胺(DCCD)是一种在温和条件下与羧基发生反应的试剂,它能以0.084 min-1的假一级速率常数(0.25 mM DCCD,37℃)不可逆地抑制(Na +,K +)-ATP酶活性(通过使用1 mM ATP进行测量)。该酶的部分活性,包括1 μM ATP时的(Na +,K +)-ATP酶、Na +-ATP酶以及酶-酰基磷酸酯(E-P)的形成,其衰减速率约为1 mM ATP时(Na +,K +)-ATP酶活性丧失速率的三分之一。无机磷酸盐形成E-P的过程不受DCCD影响,而K +-磷酸酶活性的衰减速率与1 mM ATP时测量的(Na +,K +)-ATP酶活性相同。该酶的底物(即钠、钾、镁和ATP)均降低了在1 mM或1 μM ATP下测量的(Na +,K +)-ATP酶活性的DCCD失活速率。每种底物提供的保护作用的浓度依赖性与其在催化相关位点的结合情况一致。DCCD还会使该酶交联形成非常高分子量的物种。这个过程的发生速率约为1 mM ATP时测量的(Na +,K +)-ATP酶活性丧失速率的十分之一,太慢以至于与酶活性的丧失无关。用[14C]DCCD标记该酶显示,每摩尔大亚基约掺入1摩尔DCCD;然而,掺入情况与酶活性的丧失无关。此处给出的结果表明,除了先前已知的参与E-P形成的天冬氨酸残基外,(Na +,K +)-ATP酶还含有两个对催化活性至关重要的羧基。(摘要截短至250字)

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