Number of the records: 1  

Engineering a de Novo Transport Tunnel

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    SYSNO ASEP0472361
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleEngineering a de Novo Transport Tunnel
    Author(s) Březovský, J. (CZ)
    Babková, P. (CZ)
    Degtjarik, Oksana (MBU-M)
    Fořtová, A. (CZ)
    Gora, A. (CZ)
    Iermak, Iuliia (MBU-M)
    Řezáčová, Pavlína (UMG-J) RID
    Dvořák, P. (CZ)
    Kutá Smatanová, Ivana (MBU-M) ORCID
    Prokop, Z. (CZ)
    Chaloupková, R. (CZ)
    Damborský, J. (CZ)
    Source TitleACS Catalysis. - : American Chemical Society - ISSN 2155-5435
    Roč. 6, č. 11 (2016), s. 7597-7610
    Number of pages14 s.
    Languageeng - English
    CountryUS - United States
    Keywordstransport tunnel ; protein engineering ; protein design
    Subject RIVEE - Microbiology, Virology
    Institutional supportMBU-M - RVO:61388971 ; UMG-J - RVO:68378050
    UT WOS000387306100036
    DOI10.1021/acscatal.6b02081
    AnnotationTransport of ligands between buried active sites and bulk solvent is a key step in the catalytic cycle of many enzymes. The absence of evolutionary optimized transport tunnels is an important barrier limiting the efficiency of biocatalysts prepared by computational design. Creating a structurally defined and functional "hole" into the protein represents an engineering challenge. Here we describe the computational design and directed evolution of a de novo transport tunnel in haloalkane dehalogenase. Mutants with a blocked native tunnel and newly opened auxiliary tunnel in a distinct part of the structure showed dramatically modified properties. The mutants with blocked tunnels acquired specificity never observed with native family members: up to 32 times increased substrate inhibition and 17 times reduced catalytic rates. Opening of the auxiliary tunnel resulted in specificity and substrate inhibition similar to those of the native enzyme and the most proficient haloalkane dehalogenase reported to date (k(cat) = 57 s(-1) with 1,2-dibromoethane at 37 degrees C and pH 8.6). Crystallographic analysis and molecular dynamics simulations confirmed the successful introduction of a structurally defined and functional transport tunnel. Our study demonstrates that, whereas we can open the transport tunnels with reasonable proficiency, we cannot accurately predict the effects of such change on the catalytic properties. We propose that one way to increase efficiency of an enzyme is the direct its substrates and products into spatially distinct tunnels. The results clearly show the benefits of enzymes with de novo transport tunnels, and we anticipate that this engineering strategy will facilitate the creation of a wide range of useful biocatalysts.
    WorkplaceInstitute of Microbiology
    ContactEliška Spurná, eliska.spurna@biomed.cas.cz, Tel.: 241 062 231
    Year of Publishing2017
Number of the records: 1  

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