Academic Journal

Influence of the heme distal pocket on nitrite binding orientation and reactivity in Sperm Whale myoglobin

التفاصيل البيبلوغرافية
العنوان: Influence of the heme distal pocket on nitrite binding orientation and reactivity in Sperm Whale myoglobin
المؤلفون: Tse, Wilford, Whitmore, Nathan, Cheesman, Myles R., Watmough, Nicholas J.
المصدر: Biochemical Journal ; volume 478, issue 4, page 927-942 ; ISSN 0264-6021 1470-8728
بيانات النشر: Portland Press Ltd.
سنة النشر: 2021
الوصف: Nitrite binding to recombinant wild-type Sperm Whale myoglobin (SWMb) was studied using a combination of spectroscopic methods including room-temperature magnetic circular dichroism. These revealed that the reactive species is free nitrous acid and the product of the reaction contains a nitrite ion bound to the ferric heme iron in the nitrito- (O-bound) orientation. This exists in a thermal equilibrium with a low-spin ground state and a high-spin excited state and is spectroscopically distinct from the purely low-spin nitro- (N-bound) species observed in the H64V SWMb variant. Substitution of the proximal heme ligand, histidine-93, with lysine yields a novel form of myoglobin (H93K) with enhanced reactivity towards nitrite. The nitrito-mode of binding to the ferric heme iron is retained in the H93K variant again as a thermal equilibrium of spin-states. This proximal substitution influences the heme distal pocket causing the pKa of the alkaline transition to be lowered relative to wild-type SWMb. This change in the environment of the distal pocket coupled with nitrito-binding is the most likely explanation for the 8-fold increase in the rate of nitrite reduction by H93K relative to WT SWMb.
نوع الوثيقة: article in journal/newspaper
اللغة: English
DOI: 10.1042/bcj20200596
الاتاحة: http://dx.doi.org/10.1042/bcj20200596
https://portlandpress.com/biochemj/article-pdf/478/4/927/904911/bcj-2020-0596.pdf
Rights: https://creativecommons.org/licenses/by/4.0/
رقم الانضمام: edsbas.9D35A9DA
قاعدة البيانات: BASE