Literature DB >> 28696108

Incorporating Fast Protein Dynamics into Enzyme Design: A Proposed Mutant Aromatic Amine Dehydrogenase.

Ioanna Zoi1, Dimitri Antoniou1, Steven D Schwartz1.   

Abstract

In recent years, there has been encouraging progress in the engineering of enzymes that are designed to catalyze reactions not accelerated by natural enzymes. We tested the possibility of reengineering an existing enzyme by introducing a fast protein motion that couples to the reaction. Aromatic amine dehydrogenase is a system that has been shown to use a fast substrate motion as part of the reaction mechanism. We identified a mutation that preserves this fast motion but also introduces a favorable fast motion near the active site that did not exist in the native enzyme. Transition path sampling was used for the analysis of the atomic details of the mechanism.

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Year:  2017        PMID: 28696108      PMCID: PMC5763476          DOI: 10.1021/acs.jpcb.7b05319

Source DB:  PubMed          Journal:  J Phys Chem B        ISSN: 1520-5207            Impact factor:   2.991


  32 in total

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2.  Computational design of a biologically active enzyme.

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3.  Taking Ockham's razor to enzyme dynamics and catalysis.

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4.  Computational design of an enzyme catalyst for a stereoselective bimolecular Diels-Alder reaction.

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Journal:  Science       Date:  2010-07-16       Impact factor: 47.728

5.  Atomic description of an enzyme reaction dominated by proton tunneling.

Authors:  Laura Masgrau; Anna Roujeinikova; Linus O Johannissen; Parvinder Hothi; Jaswir Basran; Kara E Ranaghan; Adrian J Mulholland; Michael J Sutcliffe; Nigel S Scrutton; David Leys
Journal:  Science       Date:  2006-04-14       Impact factor: 47.728

Review 6.  CHARMM: the biomolecular simulation program.

Authors:  B R Brooks; C L Brooks; A D Mackerell; L Nilsson; R J Petrella; B Roux; Y Won; G Archontis; C Bartels; S Boresch; A Caflisch; L Caves; Q Cui; A R Dinner; M Feig; S Fischer; J Gao; M Hodoscek; W Im; K Kuczera; T Lazaridis; J Ma; V Ovchinnikov; E Paci; R W Pastor; C B Post; J Z Pu; M Schaefer; B Tidor; R M Venable; H L Woodcock; X Wu; W Yang; D M York; M Karplus
Journal:  J Comput Chem       Date:  2009-07-30       Impact factor: 3.376

7.  The enzyme aromatic amine dehydrogenase induces a substrate conformation crucial for promoting vibration that significantly reduces the effective potential energy barrier to proton transfer.

Authors:  Linus O Johannissen; Nigel S Scrutton; Michael J Sutcliffe
Journal:  J R Soc Interface       Date:  2008-12-06       Impact factor: 4.118

8.  Modulating Enzyme Catalysis through Mutations Designed to Alter Rapid Protein Dynamics.

Authors:  Ioanna Zoi; Javier Suarez; Dimitri Antoniou; Scott A Cameron; Vern L Schramm; Steven D Schwartz
Journal:  J Am Chem Soc       Date:  2016-03-08       Impact factor: 15.419

9.  Enzyme homologues have distinct reaction paths through their transition states.

Authors:  Ioanna Zoi; Matthew W Motley; Dimitri Antoniou; Vern L Schramm; Steven D Schwartz
Journal:  J Phys Chem B       Date:  2015-02-18       Impact factor: 2.991

10.  Mechanistic studies of aromatic amine dehydrogenase, a tryptophan tryptophylquinone enzyme.

Authors:  Y L Hyun; V L Davidson
Journal:  Biochemistry       Date:  1995-01-24       Impact factor: 3.162

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  2 in total

1.  Directed Evolution as a Probe of Rate Promoting Vibrations Introduced via Mutational Change.

Authors:  Xi Chen; Steven D Schwartz
Journal:  Biochemistry       Date:  2018-03-22       Impact factor: 3.162

2.  Heavy Enzymes and the Rational Redesign of Protein Catalysts.

Authors:  Alan F Scott; Louis Y-P Luk; Iñaki Tuñón; Vicent Moliner; Rudolf K Allemann
Journal:  Chembiochem       Date:  2019-07-24       Impact factor: 3.164

  2 in total

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