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Designed for life: biocompatible de novo designed proteins and components

A principal goal of synthetic biology is the de novo design or redesign of biomolecular components. In addition to revealing fundamentally important information regarding natural biomolecular engineering and biochemistry, functional building blocks will ultimately be provided for applications includ...

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Detalles Bibliográficos
Autores principales: Grayson, Katie J., Anderson, J. L. Ross
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6127164/
https://www.ncbi.nlm.nih.gov/pubmed/30158186
http://dx.doi.org/10.1098/rsif.2018.0472
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author Grayson, Katie J.
Anderson, J. L. Ross
author_facet Grayson, Katie J.
Anderson, J. L. Ross
author_sort Grayson, Katie J.
collection PubMed
description A principal goal of synthetic biology is the de novo design or redesign of biomolecular components. In addition to revealing fundamentally important information regarding natural biomolecular engineering and biochemistry, functional building blocks will ultimately be provided for applications including the manufacture of valuable products and therapeutics. To fully realize this ambitious goal, the designed components must be biocompatible, working in concert with natural biochemical processes and pathways, while not adversely affecting cellular function. For example, de novo protein design has provided us with a wide repertoire of structures and functions, including those that can be assembled and function in vivo. Here we discuss such biocompatible designs, as well as others that have the potential to become biocompatible, including non-protein molecules, and routes to achieving full biological integration.
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spelling pubmed-61271642018-09-07 Designed for life: biocompatible de novo designed proteins and components Grayson, Katie J. Anderson, J. L. Ross J R Soc Interface Review Articles A principal goal of synthetic biology is the de novo design or redesign of biomolecular components. In addition to revealing fundamentally important information regarding natural biomolecular engineering and biochemistry, functional building blocks will ultimately be provided for applications including the manufacture of valuable products and therapeutics. To fully realize this ambitious goal, the designed components must be biocompatible, working in concert with natural biochemical processes and pathways, while not adversely affecting cellular function. For example, de novo protein design has provided us with a wide repertoire of structures and functions, including those that can be assembled and function in vivo. Here we discuss such biocompatible designs, as well as others that have the potential to become biocompatible, including non-protein molecules, and routes to achieving full biological integration. The Royal Society 2018-08 2018-08-29 /pmc/articles/PMC6127164/ /pubmed/30158186 http://dx.doi.org/10.1098/rsif.2018.0472 Text en © 2018 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Review Articles
Grayson, Katie J.
Anderson, J. L. Ross
Designed for life: biocompatible de novo designed proteins and components
title Designed for life: biocompatible de novo designed proteins and components
title_full Designed for life: biocompatible de novo designed proteins and components
title_fullStr Designed for life: biocompatible de novo designed proteins and components
title_full_unstemmed Designed for life: biocompatible de novo designed proteins and components
title_short Designed for life: biocompatible de novo designed proteins and components
title_sort designed for life: biocompatible de novo designed proteins and components
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6127164/
https://www.ncbi.nlm.nih.gov/pubmed/30158186
http://dx.doi.org/10.1098/rsif.2018.0472
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