Enantioselective [2+2]-cycloadditions with triplet photoenzymes.
Nature
; 611(7937): 715-720, 2022 11.
Article
em En
| MEDLINE
| ID: mdl-36130726
ABSTRACT
Naturally evolved enzymes, despite their astonishingly large variety and functional diversity, operate predominantly through thermochemical activation. Integrating prominent photocatalysis modes into proteins, such as triplet energy transfer, could create artificial photoenzymes that expand the scope of natural biocatalysis1-3. Here, we exploit genetically reprogrammed, chemically evolved photoenzymes embedded with a synthetic triplet photosensitizer that are capable of excited-state enantio-induction4-6. Structural optimization through four rounds of directed evolution afforded proficient variants for the enantioselective intramolecular [2+2]-photocycloaddition of indole derivatives with good substrate generality and excellent enantioselectivities (up to 99% enantiomeric excess). A crystal structure of the photoenzyme-substrate complex elucidated the non-covalent interactions that mediate the reaction stereochemistry. This study expands the energy transfer reactivity7-10 of artificial triplet photoenzymes in a supramolecular protein cavity and unlocks an integrated approach to valuable enantioselective photochemical synthesis that is not accessible with either the synthetic or the biological world alone.
Texto completo:
1
Base de dados:
MEDLINE
Assunto principal:
Enzimas
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Biocatálise
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Processos Fotoquímicos
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Reação de Cicloadição
Idioma:
En
Ano de publicação:
2022
Tipo de documento:
Article