Electric Field Measurements Reveal the Pivotal Role of Cofactor–Substrate Interaction in Dihydrofolate Reductase Catalysis
Impacto
Scholar |
Otros documentos de la autoría: Adesina, Aduragbemi S.; Świderek, Katarzyna; Luk, Louis Y. P.; Moliner, Vicent
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INVESTIGACIONMetadatos
Título
Electric Field Measurements Reveal the Pivotal Role of Cofactor–Substrate Interaction in Dihydrofolate Reductase CatalysisFecha de publicación
2020-07-17Editor
American Chemical SocietyISSN
2155-5435Cita bibliográfica
Adesina, A. S.; Świderek, K.; Luk, L. Y.; Moliner, V.; Allemann, R. K.. Electric Field Measurements Reveal the Pivotal Role of Cofactor–Substrate Interaction in Dihydrofolate Reductase Catalysis ACS Catalysis 2020 10 (14), 7907-7914 DOI: 10.1021/acscatal.0c01856Tipo de documento
info:eu-repo/semantics/articleVersión de la editorial
https://pubs.acs.org/doi/10.1021/acscatal.0c01856Versión
info:eu-repo/semantics/publishedVersionPalabras clave / Materias
Resumen
The contribution of ligand–ligand electrostatic interaction to transition state formation during enzyme catalysis has remained unexplored, even though electrostatic forces are known to play a major role in protein ... [+]
The contribution of ligand–ligand electrostatic interaction to transition state formation during enzyme catalysis has remained unexplored, even though electrostatic forces are known to play a major role in protein functions and have been investigated by the vibrational Stark effect (VSE). To monitor electrostatic changes along important steps during catalysis, we used a nitrile probe (T46C-CN) inserted proximal to the reaction center of three dihydrofolate reductases (DHFRs) with different biophysical properties, Escherichia coli DHFR (EcDHFR), its conformationally impaired variant (EcDHFR-S148P), and Geobacillus stearothermophilus DHFR (BsDHFR). Our combined experimental and computational approach revealed that the electric field projected by the substrate toward the probe negates those exerted by the cofactor when both are bound within the enzymes. This indicates that compared to previous models that focus exclusively on subdomain reorganization and protein–ligand contacts, ligand–ligand interactions are the key driving force to generate electrostatic environments conducive for catalysis. [-]
Publicado en
ACS catalysis, 2020, vol. 10, no 14Proyecto de investigación
MINECO: IJCI-201627503; Cardiff University; Biotechnology and Biological Sciences Research Council (BBSRC): BB/J005266, BB/L020394; Spanish Ministerio de Ciencia, Innovacion y Universidades: PGC2018-094852-B-C21; Generalitat Valenciana: AICO/2019/195; Universitat Jaume I: UJI~B2017-31Derechos de acceso
info:eu-repo/semantics/openAccess
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