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Dan Tawfik’s Lessons for Protein Engineers about Enzymes Adapting to New Substrates

[Image: see text] Natural evolution has been creating new complex systems for billions of years. The process is spontaneous and requires neither intelligence nor moral purpose but is nevertheless difficult to understand. The late Dan Tawfik spent years studying enzymes as they adapted to recognize n...

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Autores principales: Matsumura, Ichiro, Patrick, Wayne M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9851151/
https://www.ncbi.nlm.nih.gov/pubmed/35820168
http://dx.doi.org/10.1021/acs.biochem.2c00230
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author Matsumura, Ichiro
Patrick, Wayne M.
author_facet Matsumura, Ichiro
Patrick, Wayne M.
author_sort Matsumura, Ichiro
collection PubMed
description [Image: see text] Natural evolution has been creating new complex systems for billions of years. The process is spontaneous and requires neither intelligence nor moral purpose but is nevertheless difficult to understand. The late Dan Tawfik spent years studying enzymes as they adapted to recognize new substrates. Much of his work focused on gaining fundamental insights, so the practical utility of his experiments may not be obvious even to accomplished protein engineers. Here we focus on two questions fundamental to any directed evolution experiment. Which proteins are the best starting points for such experiments? Which trait(s) of the chosen parental protein should be evolved to achieve the desired outcome? We summarize Tawfik’s contributions to our understanding of these problems, to honor his memory and encourage those unfamiliar with his ideas to read his publications.
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spelling pubmed-98511512023-07-12 Dan Tawfik’s Lessons for Protein Engineers about Enzymes Adapting to New Substrates Matsumura, Ichiro Patrick, Wayne M. Biochemistry [Image: see text] Natural evolution has been creating new complex systems for billions of years. The process is spontaneous and requires neither intelligence nor moral purpose but is nevertheless difficult to understand. The late Dan Tawfik spent years studying enzymes as they adapted to recognize new substrates. Much of his work focused on gaining fundamental insights, so the practical utility of his experiments may not be obvious even to accomplished protein engineers. Here we focus on two questions fundamental to any directed evolution experiment. Which proteins are the best starting points for such experiments? Which trait(s) of the chosen parental protein should be evolved to achieve the desired outcome? We summarize Tawfik’s contributions to our understanding of these problems, to honor his memory and encourage those unfamiliar with his ideas to read his publications. American Chemical Society 2022-07-12 /pmc/articles/PMC9851151/ /pubmed/35820168 http://dx.doi.org/10.1021/acs.biochem.2c00230 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Matsumura, Ichiro
Patrick, Wayne M.
Dan Tawfik’s Lessons for Protein Engineers about Enzymes Adapting to New Substrates
title Dan Tawfik’s Lessons for Protein Engineers about Enzymes Adapting to New Substrates
title_full Dan Tawfik’s Lessons for Protein Engineers about Enzymes Adapting to New Substrates
title_fullStr Dan Tawfik’s Lessons for Protein Engineers about Enzymes Adapting to New Substrates
title_full_unstemmed Dan Tawfik’s Lessons for Protein Engineers about Enzymes Adapting to New Substrates
title_short Dan Tawfik’s Lessons for Protein Engineers about Enzymes Adapting to New Substrates
title_sort dan tawfik’s lessons for protein engineers about enzymes adapting to new substrates
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9851151/
https://www.ncbi.nlm.nih.gov/pubmed/35820168
http://dx.doi.org/10.1021/acs.biochem.2c00230
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