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Environmental Calcium Controls Alternate Physical States of the Caulobacter Surface Layer

Surface layers (S-layers) are paracrystalline, proteinaceous structures found in most archaea and many bacteria. Often the outermost cell envelope component, S-layers serve diverse functions including aiding pathogenicity and protecting against predators. We report that the S-layer of Caulobacter cr...

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Autores principales: Herrmann, Jonathan, Jabbarpour, Fatemeh, Bargar, Paul G., Nomellini, John F., Li, Po-Nan, Lane, Thomas J., Weiss, Thomas M., Smit, John, Shapiro, Lucy, Wakatsuki, Soichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Biophysical Society 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5425405/
https://www.ncbi.nlm.nih.gov/pubmed/28494955
http://dx.doi.org/10.1016/j.bpj.2017.04.003
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author Herrmann, Jonathan
Jabbarpour, Fatemeh
Bargar, Paul G.
Nomellini, John F.
Li, Po-Nan
Lane, Thomas J.
Weiss, Thomas M.
Smit, John
Shapiro, Lucy
Wakatsuki, Soichi
author_facet Herrmann, Jonathan
Jabbarpour, Fatemeh
Bargar, Paul G.
Nomellini, John F.
Li, Po-Nan
Lane, Thomas J.
Weiss, Thomas M.
Smit, John
Shapiro, Lucy
Wakatsuki, Soichi
author_sort Herrmann, Jonathan
collection PubMed
description Surface layers (S-layers) are paracrystalline, proteinaceous structures found in most archaea and many bacteria. Often the outermost cell envelope component, S-layers serve diverse functions including aiding pathogenicity and protecting against predators. We report that the S-layer of Caulobacter crescentus exhibits calcium-mediated structural plasticity, switching irreversibly between an amorphous aggregate state and the crystalline state. This finding invalidates the common assumption that S-layers serve only as static wall-like structures. In vitro, the Caulobacter S-layer protein, RsaA, enters the aggregate state at physiological temperatures and low divalent calcium ion concentrations. At higher concentrations, calcium ions stabilize monomeric RsaA, which can then transition to the two-dimensional crystalline state. Caulobacter requires micromolar concentrations of calcium for normal growth and development. Without an S-layer, Caulobacter is even more sensitive to changes in environmental calcium concentration. Therefore, this structurally dynamic S-layer responds to environmental conditions as an ion sensor and protects Caulobacter from calcium deficiency stress, a unique mechanism of bacterial adaptation. These findings provide a biochemical and physiological basis for RsaA’s calcium-binding behavior, which extends far beyond calcium’s commonly accepted role in aiding S-layer biogenesis or oligomerization and demonstrates a connection to cellular fitness.
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spelling pubmed-54254052018-05-09 Environmental Calcium Controls Alternate Physical States of the Caulobacter Surface Layer Herrmann, Jonathan Jabbarpour, Fatemeh Bargar, Paul G. Nomellini, John F. Li, Po-Nan Lane, Thomas J. Weiss, Thomas M. Smit, John Shapiro, Lucy Wakatsuki, Soichi Biophys J Proteins Surface layers (S-layers) are paracrystalline, proteinaceous structures found in most archaea and many bacteria. Often the outermost cell envelope component, S-layers serve diverse functions including aiding pathogenicity and protecting against predators. We report that the S-layer of Caulobacter crescentus exhibits calcium-mediated structural plasticity, switching irreversibly between an amorphous aggregate state and the crystalline state. This finding invalidates the common assumption that S-layers serve only as static wall-like structures. In vitro, the Caulobacter S-layer protein, RsaA, enters the aggregate state at physiological temperatures and low divalent calcium ion concentrations. At higher concentrations, calcium ions stabilize monomeric RsaA, which can then transition to the two-dimensional crystalline state. Caulobacter requires micromolar concentrations of calcium for normal growth and development. Without an S-layer, Caulobacter is even more sensitive to changes in environmental calcium concentration. Therefore, this structurally dynamic S-layer responds to environmental conditions as an ion sensor and protects Caulobacter from calcium deficiency stress, a unique mechanism of bacterial adaptation. These findings provide a biochemical and physiological basis for RsaA’s calcium-binding behavior, which extends far beyond calcium’s commonly accepted role in aiding S-layer biogenesis or oligomerization and demonstrates a connection to cellular fitness. The Biophysical Society 2017-05-09 2017-05-09 /pmc/articles/PMC5425405/ /pubmed/28494955 http://dx.doi.org/10.1016/j.bpj.2017.04.003 Text en © 2017 Biophysical Society. 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 Proteins
Herrmann, Jonathan
Jabbarpour, Fatemeh
Bargar, Paul G.
Nomellini, John F.
Li, Po-Nan
Lane, Thomas J.
Weiss, Thomas M.
Smit, John
Shapiro, Lucy
Wakatsuki, Soichi
Environmental Calcium Controls Alternate Physical States of the Caulobacter Surface Layer
title Environmental Calcium Controls Alternate Physical States of the Caulobacter Surface Layer
title_full Environmental Calcium Controls Alternate Physical States of the Caulobacter Surface Layer
title_fullStr Environmental Calcium Controls Alternate Physical States of the Caulobacter Surface Layer
title_full_unstemmed Environmental Calcium Controls Alternate Physical States of the Caulobacter Surface Layer
title_short Environmental Calcium Controls Alternate Physical States of the Caulobacter Surface Layer
title_sort environmental calcium controls alternate physical states of the caulobacter surface layer
topic Proteins
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5425405/
https://www.ncbi.nlm.nih.gov/pubmed/28494955
http://dx.doi.org/10.1016/j.bpj.2017.04.003
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