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亚硝酸盐与珠蛋白的结合:键合异构、电子顺磁共振沉默及还原化学

Nitrite binding to globins: linkage isomerism, EPR silence and reductive chemistry.

作者信息

Silaghi-Dumitrescu Radu, Svistunenko Dimitri A, Cioloboc Daniela, Bischin Cristina, Scurtu Florina, Cooper Chris E

机构信息

"Babeş-Bolyai" University, 1 Mihail Kogalniceanu str., RO-400084 Cluj-Napoca, Romania; Department of Biological Sciences, University of Essex, Wivenhoe Park, Colchester, Essex CO4 3SQ, UK.

Department of Biological Sciences, University of Essex, Wivenhoe Park, Colchester, Essex CO4 3SQ, UK.

出版信息

Nitric Oxide. 2014 Nov 15;42:32-9. doi: 10.1016/j.niox.2014.08.007. Epub 2014 Aug 27.

Abstract

The nitrite adducts of globins can potentially bind via O- or N- linkage to the heme iron. We have used EPR (electron paramagnetic resonance) and DFT (density functional theory) to explore these binding modes to myoglobin and hemoglobin. We demonstrate that the nitrite adducts of both globins have detectable EPR signals; we provide an explanation for the difficulty in detecting these EPR features, based on uniaxial state considerations. The EPR and DFT data show that both nitrite linkage isomers can be present at the same time and that the two isomers are readily interconvertible in solution. The millisecond-scale process of nitrite reduction by Hb is investigated in search of the elusive Fe(II)-nitrite adduct.

摘要

珠蛋白的亚硝酸盐加合物可能通过O-或N-键与血红素铁结合。我们利用电子顺磁共振(EPR)和密度泛函理论(DFT)来探究这些与肌红蛋白和血红蛋白的结合模式。我们证明两种珠蛋白的亚硝酸盐加合物都有可检测到的EPR信号;基于单轴状态的考虑,我们对检测这些EPR特征的困难给出了解释。EPR和DFT数据表明,两种亚硝酸盐连接异构体可以同时存在,并且这两种异构体在溶液中很容易相互转化。为了寻找难以捉摸的Fe(II)-亚硝酸盐加合物,我们研究了血红蛋白还原亚硝酸盐的毫秒级过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77c3/4256065/c64b46e00281/yniox1409-ga-5001.jpg

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