Chemical Ligation and Isotope Labeling to Locate Dynamic Effects during Catalysis by Dihydrofolate Reductase
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Otros documentos de la autoría: Luk, Louis Y. P.; Ruiz-Pernía, José Javier; Adesina, Aduragbemi S.; Loveridge, E. Joel; Tuñón, Iñaki; Moliner, Vicent; Allemann, Rudolf K.
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Título
Chemical Ligation and Isotope Labeling to Locate Dynamic Effects during Catalysis by Dihydrofolate ReductaseAutoría
Fecha de publicación
2015-07-27Editor
WileyCita bibliográfica
LUK, Louis Y. P.; RUIZ PERNÍA, J. Javier; ADESINA, Aduragbemi S.; LOVERIDGE, E. Joel; TUÑÓN, Iñaki; MOLINER IBÁÑEZ, Vicent; ALLEMANN, Rudolk K..Chemical Ligation and Isotope Labeling to Locate Dynamic Effects during Catalysis by Dihydrofolate Reductase. Angewandte Chemie (2015), v. 54, issue 31, pp. 9016-9020Tipo de documento
info:eu-repo/semantics/articleVersión de la editorial
http://onlinelibrary.wiley.com/doi/10.1002/anie.v54.31/issuetocVersión
info:eu-repo/semantics/acceptedVersionPalabras clave / Materias
Resumen
Experimental and computational approaches have long been employed to define the role of protein motions in en- zyme catalysis, but a refined experimental method for locating the origin of dynamic effects has not ... [+]
Experimental and computational approaches have long been employed to define the role of protein motions in en- zyme catalysis, but a refined experimental method for locating the origin of dynamic effects has not previously been developed. Here a general synthetic approach is described to alter motions in specific regions of an enzyme and to analyze the effects of such localized motional changes by measuring ‘segment kinetic isotope effects’. Two isotopic hybrids of dihydrofolate reductase from Escherichia coli (EcDHFR) were prepared by chemical ligation; one with the mobile N-terminal segment (amino acids 1-28) con- taining heavy isotopes (2H, 13C, 15N) and the remainder of the protein (amino acids 29-159) with natural isotopic abundance, and the complementary hybrid with the C-terminal segment isotopically labeled. Investigation of the catalytic properties of these hybrids indicated that isotopic substitution of the N-terminal segment affects a physical step of catalysis, whereas the hydride transfer itself is affected by dynamic effects originating from residues 29-159. To verify the effectiveness of this method and to decipher its mechanistic basis, the experimental results were complemented with QM/MM computational studies, rendering a good agreement with experiments and supporting the idea of small dynamic effects on catalysis originated on the C-terminal segment. which indi- cated that segment isotope labeling affects the recrossing trajectories on the reaction barrier. By isolating the effect of the motions of individual regions of the enzyme on the observed rate constants, segment kinetic isotope effects provide insight difficult to ob- tain with other experimental methods. Measurements of segment kinetic isotope effects will help to define the dynamic networks of intramolecular interactions central to enzyme catalysis. [-]
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Angewandte Chemie (2015), v. 54, issue 31Derechos de acceso
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info:eu-repo/semantics/openAccess
info:eu-repo/semantics/openAccess
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