Molecular Gating of an Engineered Enzyme Captured in Real Time
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14310%2F18%3A00101750" target="_blank" >RIV/00216224:14310/18:00101750 - isvavai.cz</a>
Alternative codes found
RIV/61388971:_____/18:00500166 RIV/61388955:_____/18:00498928 RIV/00159816:_____/18:00069367
Result on the web
<a href="http://dx.doi.org/10.1021/jacs.8b09848" target="_blank" >http://dx.doi.org/10.1021/jacs.8b09848</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1021/jacs.8b09848" target="_blank" >10.1021/jacs.8b09848</a>
Alternative languages
Result language
angličtina
Original language name
Molecular Gating of an Engineered Enzyme Captured in Real Time
Original language description
Enzyme engineering tends to focus on the design of active sites for the chemical steps, while the physical steps of the catalytic cycle are often overlooked. Tight binding of a substrate in an active site is beneficial for the chemical steps, whereas good accessibility benefits substrate binding and product release. Many enzymes control the accessibility of their active sites by molecular gates. Here we analyzed the dynamics of a molecular gate artificially introduced into an access tunnel of the most efficient haloalkane dehalogenase using pre-steady-state kinetics, single-molecule fluorescence spectroscopy, and molecular dynamics. Photoinduced electron-transfer fluorescence correlation spectroscopy (PET-FCS) has enabled real-time observation of molecular gating at the single-molecule level with rate constants (k(on) = 1822 s(-1), k(off) = 60 s(-1)) corresponding well with those from the pre-steady-state kinetics (k(-1) = 1100 s(-1), k(1) = 20 s(-1)). The PET-FCS technique is used here to study the conformational dynamics in a soluble enzyme, thus demonstrating an additional application for this method. Engineering dynamical molecular gates represents a widely applicable strategy for designing efficient biocatalysts.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
10401 - Organic chemistry
Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2018
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Journal of the American Chemical Society
ISSN
0002-7863
e-ISSN
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Volume of the periodical
140
Issue of the periodical within the volume
51
Country of publishing house
US - UNITED STATES
Number of pages
10
Pages from-to
17999-18008
UT code for WoS article
000454751800028
EID of the result in the Scopus database
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