Tocheva Elitza I, Rosell Federico I, Mauk A Grant, Murphy Michael E P
Department of Microbiology and Immunology, The University of British Columbia, Vancouver, BC, Canada V6T 1Z3.
Science. 2004 May 7;304(5672):867-70. doi: 10.1126/science.1095109.
A copper-nitrosyl intermediate forms during the catalytic cycle of nitrite reductase, the enzyme that mediates the committed step in bacterial denitrification. The crystal structure of a type 2 copper-nitrosyl complex of nitrite reductase reveals an unprecedented side-on binding mode in which the nitrogen and oxygen atoms are nearly equidistant from the copper cofactor. Comparison of this structure with a refined nitrite-bound crystal structure explains how coordination can change between copper-oxygen and copper-nitrogen during catalysis. The side-on copper-nitrosyl in nitrite reductase expands the possibilities for nitric oxide interactions in copper proteins such as superoxide dismutase and prions.
在亚硝酸还原酶的催化循环过程中会形成一种铜-亚硝酰中间体,亚硝酸还原酶是介导细菌反硝化作用关键步骤的酶。亚硝酸还原酶的一种2型铜-亚硝酰配合物的晶体结构揭示了一种前所未有的侧面结合模式,其中氮原子和氧原子与铜辅因子的距离几乎相等。将该结构与优化后的亚硝酸结合晶体结构进行比较,解释了催化过程中铜-氧配位和铜-氮配位之间是如何转变的。亚硝酸还原酶中的侧面铜-亚硝酰配合物拓展了铜蛋白(如超氧化物歧化酶和朊病毒)中一氧化氮相互作用的可能性。