Proteins as templates for complex synthetic metalloclusters: towards biologically programmed heterogeneous catalysis

Despite nature’s prevalent use of metals as prosthetics to adapt or enhance the behaviour of proteins, our ability to programme such architectural organization remains underdeveloped. Multi-metal clusters buried in proteins underpin the most remarkable chemical transformations in nature, but we are...

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Main Authors: Fehl, C, Davis, B
Format: Journal article
Language:English
Published: Royal Society 2016
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author Fehl, C
Davis, B
author_facet Fehl, C
Davis, B
author_sort Fehl, C
collection OXFORD
description Despite nature’s prevalent use of metals as prosthetics to adapt or enhance the behaviour of proteins, our ability to programme such architectural organization remains underdeveloped. Multi-metal clusters buried in proteins underpin the most remarkable chemical transformations in nature, but we are not yet in a position to fully mimic or exploit such systems. With the advent of copious, relevant structural information, judicious mechanistic studies and the use of accessible computational methods in protein design coupled with new synthetic methods for building biomacromolecules, we can envisage a ‘new dawn’ that will allow us to build de novo metalloenzymes that move beyond mono-metal centres. In particular, we highlight the need for systems that approach the multi-centred clusters that have evolved to couple electron shuttling with catalysis. Such hybrids may be viewed as exciting mid-points between homogeneous and heterogeneous catalysts which also exploit the primary benefits of biocatalysis.
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spelling oxford-uuid:ba2bad52-b22e-4fe6-b918-3261480f077c2022-03-27T05:08:04ZProteins as templates for complex synthetic metalloclusters: towards biologically programmed heterogeneous catalysisJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:ba2bad52-b22e-4fe6-b918-3261480f077cEnglishSymplectic Elements at OxfordRoyal Society2016Fehl, CDavis, BDespite nature’s prevalent use of metals as prosthetics to adapt or enhance the behaviour of proteins, our ability to programme such architectural organization remains underdeveloped. Multi-metal clusters buried in proteins underpin the most remarkable chemical transformations in nature, but we are not yet in a position to fully mimic or exploit such systems. With the advent of copious, relevant structural information, judicious mechanistic studies and the use of accessible computational methods in protein design coupled with new synthetic methods for building biomacromolecules, we can envisage a ‘new dawn’ that will allow us to build de novo metalloenzymes that move beyond mono-metal centres. In particular, we highlight the need for systems that approach the multi-centred clusters that have evolved to couple electron shuttling with catalysis. Such hybrids may be viewed as exciting mid-points between homogeneous and heterogeneous catalysts which also exploit the primary benefits of biocatalysis.
spellingShingle Fehl, C
Davis, B
Proteins as templates for complex synthetic metalloclusters: towards biologically programmed heterogeneous catalysis
title Proteins as templates for complex synthetic metalloclusters: towards biologically programmed heterogeneous catalysis
title_full Proteins as templates for complex synthetic metalloclusters: towards biologically programmed heterogeneous catalysis
title_fullStr Proteins as templates for complex synthetic metalloclusters: towards biologically programmed heterogeneous catalysis
title_full_unstemmed Proteins as templates for complex synthetic metalloclusters: towards biologically programmed heterogeneous catalysis
title_short Proteins as templates for complex synthetic metalloclusters: towards biologically programmed heterogeneous catalysis
title_sort proteins as templates for complex synthetic metalloclusters towards biologically programmed heterogeneous catalysis
work_keys_str_mv AT fehlc proteinsastemplatesforcomplexsyntheticmetalloclusterstowardsbiologicallyprogrammedheterogeneouscatalysis
AT davisb proteinsastemplatesforcomplexsyntheticmetalloclusterstowardsbiologicallyprogrammedheterogeneouscatalysis