官能酰环化酶:NO击中目标。

Michael Russwurm, Doris Koesling
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引用次数: 44

摘要

NO受体,即NO敏感的guananyyl环化酶,在NO/cGMP信号转导级联中起关键作用。目前已知该酶的两种异构体,广泛分布于血管的alpha1beta1异构体和主要在大脑中表达的神经元的alpha2beta1异构体。与PSD-95(突触后密度蛋白-95)支架蛋白家族的相互作用将神经元α 2 β 1亚型靶向突触膜。官能基环化酶的NO传感器由假体血红素组形成,在那里NO结合发生并诱导酶的高达200倍的激活。血红素组允许NO对酶活性进行严格调节,并且代表了该酶最显著的特征,因为它在许多方面不同于其他血红蛋白的血红素组。新的NO增敏剂如YC-1[3-(5'-羟甲基-2'-呋喃基)-1-苄基唑]影响NO和CO的活化作用,其机制目前正在深入研究中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Guanylyl cyclase: NO hits its target.

The NO receptor, NO-sensitive guanylyl cyclase, plays a key role in the NO/cGMP signal-transduction cascade. Two isoforms of the enzyme are currently known, the widely distributed vascular alpha1beta1 isoform and the neuronal alpha2beta1 isoform predominantly expressed in brain. Interaction with the PSD-95 (postsynaptic density protein-95) family of scaffolding proteins targets the neuronal alpha2beta1 isoform to synaptic membranes. The NO sensor of the guanylyl cyclase is formed by the prosthetic haem group, where NO binding takes place and induces the up to 200-fold activation of the enzyme. The haem group allows tight regulation of enzymic activity by NO and represents the most striking feature of the enzyme, as it differs in many aspects from the well-characterized haem groups of other haemoproteins. The new NO sensitizers such as YC-1 [3-(5'-hydroxymethyl-2'-furyl)-1-benzylindazole] affect activation by NO and CO by mechanisms that are currently subject to intense research.

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