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Unfolding the Mysteries of Protein Metamorphosis

[Image: see text] Since the proposal of Anfinsen’s thermodynamic hypothesis in 1963, our understanding of protein folding and dynamics has gained significant appreciation of its nuance and complexity. Intrinsically disordered proteins, chameleonic sequences, morpheeins, and metamorphic proteins have...

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Detalles Bibliográficos
Autores principales: Dishman, Acacia F., Volkman, Brian F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6007232/
https://www.ncbi.nlm.nih.gov/pubmed/29787234
http://dx.doi.org/10.1021/acschembio.8b00276
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author Dishman, Acacia F.
Volkman, Brian F.
author_facet Dishman, Acacia F.
Volkman, Brian F.
author_sort Dishman, Acacia F.
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description [Image: see text] Since the proposal of Anfinsen’s thermodynamic hypothesis in 1963, our understanding of protein folding and dynamics has gained significant appreciation of its nuance and complexity. Intrinsically disordered proteins, chameleonic sequences, morpheeins, and metamorphic proteins have broadened the protein folding paradigm. Here, we discuss noncanonical protein folding patterns, with an emphasis on metamorphic proteins, and we review known metamorphic proteins that occur naturally and that have been engineered in the laboratory. Finally, we discuss research areas surrounding metamorphic proteins that are primed for future exploration, including evolution, drug discovery, and the quest for previously unrecognized metamorphs. As we enter an age where we are capable of complex bioinformatic searches and de novo protein design, we are primed to search for previously unrecognized metamorphic proteins and to design our own metamorphs to act as targeted, switchable drugs; biosensors; and more.
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spelling pubmed-60072322019-05-22 Unfolding the Mysteries of Protein Metamorphosis Dishman, Acacia F. Volkman, Brian F. ACS Chem Biol [Image: see text] Since the proposal of Anfinsen’s thermodynamic hypothesis in 1963, our understanding of protein folding and dynamics has gained significant appreciation of its nuance and complexity. Intrinsically disordered proteins, chameleonic sequences, morpheeins, and metamorphic proteins have broadened the protein folding paradigm. Here, we discuss noncanonical protein folding patterns, with an emphasis on metamorphic proteins, and we review known metamorphic proteins that occur naturally and that have been engineered in the laboratory. Finally, we discuss research areas surrounding metamorphic proteins that are primed for future exploration, including evolution, drug discovery, and the quest for previously unrecognized metamorphs. As we enter an age where we are capable of complex bioinformatic searches and de novo protein design, we are primed to search for previously unrecognized metamorphic proteins and to design our own metamorphs to act as targeted, switchable drugs; biosensors; and more. American Chemical Society 2018-05-22 2018-06-15 /pmc/articles/PMC6007232/ /pubmed/29787234 http://dx.doi.org/10.1021/acschembio.8b00276 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Dishman, Acacia F.
Volkman, Brian F.
Unfolding the Mysteries of Protein Metamorphosis
title Unfolding the Mysteries of Protein Metamorphosis
title_full Unfolding the Mysteries of Protein Metamorphosis
title_fullStr Unfolding the Mysteries of Protein Metamorphosis
title_full_unstemmed Unfolding the Mysteries of Protein Metamorphosis
title_short Unfolding the Mysteries of Protein Metamorphosis
title_sort unfolding the mysteries of protein metamorphosis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6007232/
https://www.ncbi.nlm.nih.gov/pubmed/29787234
http://dx.doi.org/10.1021/acschembio.8b00276
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