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Expanding the chemical diversity of M13 bacteriophage

Bacteriophage M13 virions are very stable nanoparticles that can be modified by chemical and genetic methods. The capsid proteins can be functionalized in a variety of chemical reactions without loss of particle integrity. In addition, Genetic Code Expansion (GCE) permits the introduction of non-can...

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Autores principales: Allen, Grace L., Grahn, Ashley K., Kourentzi, Katerina, Willson, Richard C., Waldrop, Sean, Guo, Jiantao, Kay, Brian K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9393631/
https://www.ncbi.nlm.nih.gov/pubmed/36003937
http://dx.doi.org/10.3389/fmicb.2022.961093
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author Allen, Grace L.
Grahn, Ashley K.
Kourentzi, Katerina
Willson, Richard C.
Waldrop, Sean
Guo, Jiantao
Kay, Brian K.
author_facet Allen, Grace L.
Grahn, Ashley K.
Kourentzi, Katerina
Willson, Richard C.
Waldrop, Sean
Guo, Jiantao
Kay, Brian K.
author_sort Allen, Grace L.
collection PubMed
description Bacteriophage M13 virions are very stable nanoparticles that can be modified by chemical and genetic methods. The capsid proteins can be functionalized in a variety of chemical reactions without loss of particle integrity. In addition, Genetic Code Expansion (GCE) permits the introduction of non-canonical amino acids (ncAAs) into displayed peptides and proteins. The incorporation of ncAAs into phage libraries has led to the discovery of high-affinity binders with low nanomolar dissociation constant (K(D)) values that can potentially serve as inhibitors. This article reviews how bioconjugation and the incorporation of ncAAs during translation have expanded the chemistry of peptides and proteins displayed by M13 virions for a variety of purposes.
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spelling pubmed-93936312022-08-23 Expanding the chemical diversity of M13 bacteriophage Allen, Grace L. Grahn, Ashley K. Kourentzi, Katerina Willson, Richard C. Waldrop, Sean Guo, Jiantao Kay, Brian K. Front Microbiol Microbiology Bacteriophage M13 virions are very stable nanoparticles that can be modified by chemical and genetic methods. The capsid proteins can be functionalized in a variety of chemical reactions without loss of particle integrity. In addition, Genetic Code Expansion (GCE) permits the introduction of non-canonical amino acids (ncAAs) into displayed peptides and proteins. The incorporation of ncAAs into phage libraries has led to the discovery of high-affinity binders with low nanomolar dissociation constant (K(D)) values that can potentially serve as inhibitors. This article reviews how bioconjugation and the incorporation of ncAAs during translation have expanded the chemistry of peptides and proteins displayed by M13 virions for a variety of purposes. Frontiers Media S.A. 2022-08-08 /pmc/articles/PMC9393631/ /pubmed/36003937 http://dx.doi.org/10.3389/fmicb.2022.961093 Text en Copyright © 2022 Allen, Grahn, Kourentzi, Willson, Waldrop, Guo and Kay. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Allen, Grace L.
Grahn, Ashley K.
Kourentzi, Katerina
Willson, Richard C.
Waldrop, Sean
Guo, Jiantao
Kay, Brian K.
Expanding the chemical diversity of M13 bacteriophage
title Expanding the chemical diversity of M13 bacteriophage
title_full Expanding the chemical diversity of M13 bacteriophage
title_fullStr Expanding the chemical diversity of M13 bacteriophage
title_full_unstemmed Expanding the chemical diversity of M13 bacteriophage
title_short Expanding the chemical diversity of M13 bacteriophage
title_sort expanding the chemical diversity of m13 bacteriophage
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9393631/
https://www.ncbi.nlm.nih.gov/pubmed/36003937
http://dx.doi.org/10.3389/fmicb.2022.961093
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