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Clickable methionine as a universal probe for labelling intracellular bacteria

Despite their clinical and biological importance, the cell biology of obligate intracellular bacteria is less well understood than that of many free-living model organisms. One reason for this is that they are mostly genetically intractable. As a consequence, it is not possible to engineer strains e...

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Detalles Bibliográficos
Autores principales: Atwal, Sharanjeet, Giengkam, Suparat, Jaiyen, Yanin, Feaga, Heather A., Dworkin, Jonathan, Salje, Jeanne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Biomedical 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6996152/
https://www.ncbi.nlm.nih.gov/pubmed/31862457
http://dx.doi.org/10.1016/j.mimet.2019.105812
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author Atwal, Sharanjeet
Giengkam, Suparat
Jaiyen, Yanin
Feaga, Heather A.
Dworkin, Jonathan
Salje, Jeanne
author_facet Atwal, Sharanjeet
Giengkam, Suparat
Jaiyen, Yanin
Feaga, Heather A.
Dworkin, Jonathan
Salje, Jeanne
author_sort Atwal, Sharanjeet
collection PubMed
description Despite their clinical and biological importance, the cell biology of obligate intracellular bacteria is less well understood than that of many free-living model organisms. One reason for this is that they are mostly genetically intractable. As a consequence, it is not possible to engineer strains expressing fluorescent proteins and therefore fluorescence light microscopy – a key tool in host-pathogen cell biology studies – is difficult. Strain diversity also limits the universality of antibody-based immunofluorescence approaches. Here, we have developed a universal labelling protocol for intracellular bacteria based on a clickable methionine analog. Whilst we have applied this to obligate intracellular bacteria, we expect it to be useful for labelling free living bacteria as well as other intracellular pathogens.
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spelling pubmed-69961522020-02-05 Clickable methionine as a universal probe for labelling intracellular bacteria Atwal, Sharanjeet Giengkam, Suparat Jaiyen, Yanin Feaga, Heather A. Dworkin, Jonathan Salje, Jeanne J Microbiol Methods Article Despite their clinical and biological importance, the cell biology of obligate intracellular bacteria is less well understood than that of many free-living model organisms. One reason for this is that they are mostly genetically intractable. As a consequence, it is not possible to engineer strains expressing fluorescent proteins and therefore fluorescence light microscopy – a key tool in host-pathogen cell biology studies – is difficult. Strain diversity also limits the universality of antibody-based immunofluorescence approaches. Here, we have developed a universal labelling protocol for intracellular bacteria based on a clickable methionine analog. Whilst we have applied this to obligate intracellular bacteria, we expect it to be useful for labelling free living bacteria as well as other intracellular pathogens. Elsevier Biomedical 2020-02 /pmc/articles/PMC6996152/ /pubmed/31862457 http://dx.doi.org/10.1016/j.mimet.2019.105812 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Atwal, Sharanjeet
Giengkam, Suparat
Jaiyen, Yanin
Feaga, Heather A.
Dworkin, Jonathan
Salje, Jeanne
Clickable methionine as a universal probe for labelling intracellular bacteria
title Clickable methionine as a universal probe for labelling intracellular bacteria
title_full Clickable methionine as a universal probe for labelling intracellular bacteria
title_fullStr Clickable methionine as a universal probe for labelling intracellular bacteria
title_full_unstemmed Clickable methionine as a universal probe for labelling intracellular bacteria
title_short Clickable methionine as a universal probe for labelling intracellular bacteria
title_sort clickable methionine as a universal probe for labelling intracellular bacteria
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6996152/
https://www.ncbi.nlm.nih.gov/pubmed/31862457
http://dx.doi.org/10.1016/j.mimet.2019.105812
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