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From Synthetic to Biological Fe 4 S 4 Complexes: Redox Properties Correlated to Function of Radical S‐Adenosylmethionine Enzymes
Author(s) -
Bím Daniel,
AlonsoGil Santiago,
Srnec Martin
Publication year - 2020
Publication title -
chempluschem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.801
H-Index - 61
ISSN - 2192-6506
DOI - 10.1002/cplu.202000663
Subject(s) - chemistry , redox , hydrogen atom abstraction , hydrogen atom , enzyme , function (biology) , aqueous solution , radical ion , radical , combinatorial chemistry , computational chemistry , organic chemistry , group (periodic table) , ion , evolutionary biology , biology
By employing the computational protocol for calculation of reduction potentials of the Fe 4 S 4 ‐containing species validated using a representative series of well‐defined synthetic complexes, we focused on redox properties of two prototypical radical SAM enzymes to reveal how they transform SAM into the reactive 5’‐deoxyadenosyl radical, and how they tune this radical for its proper biological function. We found the reduction potential of SAM is indeed elevated by 0.3–0.4 V upon coordination to Fe 4 S 4 , which was previously speculated in the literature. This makes a generation of 5’‐deoxyadenosyl radical from SAM less endergonic (by ca. 7–9 kcal mol −1 ) and hence more feasible in both enzymes as compared to the identical process in water. Furthermore, our calculations indicate that the enzyme‐bound 5’‐deoxyadenosyl radical has a significantly lower reduction potential than in referential aqueous solution, which may help the enzymes to suppress potential side redox reactions and simultaneously elevate its proton‐philic character, which may, in turn, promote the radical hydrogen‐atom abstraction ability.