Ferric heme as a CO/NO sensor in the nuclear receptor Rev-Erbß by coupling gas binding to electron transfer.

Autor:	Sarkar A; Department of Biological Chemistry, University of Michigan, Ann Arbor, MI 48109., Carter EL; Department of Biological Chemistry, University of Michigan, Ann Arbor, MI 48109., Harland JB; Department of Chemistry, University of Michigan, Ann Arbor, MI 48109., Speelman AL; Department of Chemistry, University of Michigan, Ann Arbor, MI 48109.; Department of Biophysics, University of Michigan, Ann Arbor, MI 48109., Lehnert N; Department of Chemistry, University of Michigan, Ann Arbor, MI 48109., Ragsdale SW; Department of Biological Chemistry, University of Michigan, Ann Arbor, MI 48109; sragsdal@umich.edu.
Jazyk:	angličtina
Zdroj:	Proceedings of the National Academy of Sciences of the United States of America [Proc Natl Acad Sci U S A] 2021 Jan 19; Vol. 118 (3).
DOI:	10.1073/pnas.2016717118
Abstrakt:	Rev-Erbβ is a nuclear receptor that couples circadian rhythm, metabolism, and inflammation. Heme binding to the protein modulates its function as a repressor, its stability, its ability to bind other proteins, and its activity in gas sensing. Rev-Erbβ binds Fe 3+ -heme more tightly than Fe 2+ -heme, suggesting its activities may be regulated by the heme redox state. Yet, this critical role of heme redox chemistry in defining the protein's resting state and function is unknown. We demonstrate by electrochemical and whole-cell electron paramagnetic resonance experiments that Rev-Erbβ exists in the Fe 3+ form within the cell allowing the protein to be heme replete even at low concentrations of labile heme in the nucleus. However, being in the Fe 3+ redox state contradicts Rev-Erb's known function as a gas sensor, which dogma asserts must be Fe 2+ This paper explains why the resting Fe 3+ state is congruent both with heme binding and cellular gas sensing. We show that the binding of CO/NO elicits a striking increase in the redox potential of the Fe 3+ /Fe 2+ couple, characteristic of an EC mechanism in which the unfavorable E lectrochemical reduction of heme is coupled to the highly favorable C hemical reaction of gas binding, making the reduction spontaneous. Thus, Fe 3+ -Rev-Erbβ remains heme-loaded, crucial for its repressor activity, and undergoes reduction when diatomic gases are present. This work has broad implications for proteins in which ligand-triggered redox changes cause conformational changes influencing its function or interprotein interactions (e.g., between NCoR1 and Rev-Erbβ). This study opens up the possibility of CO/NO-mediated regulation of the circadian rhythm through redox changes in Rev-Erbβ. Competing Interests: The authors declare no competing interest.
Databáze:	MEDLINE
Externí odkaz:	Zobrazit plný text záznamu