Cargando…

Atomic Force Microscopy of Photosystem II and Its Unit Cell Clustering Quantitatively Delineate the Mesoscale Variability in Arabidopsis Thylakoids

Photoautotrophic organisms efficiently regulate absorption of light energy to sustain photochemistry while promoting photoprotection. Photoprotection is achieved in part by triggering a series of dissipative processes termed non-photochemical quenching (NPQ), which depend on the re-organization of p...

Descripción completa

Detalles Bibliográficos
Autores principales: Onoa, Bibiana, Schneider, Anna R., Brooks, Matthew D., Grob, Patricia, Nogales, Eva, Geissler, Phillip L., Niyogi, Krishna K., Bustamante, Carlos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4090009/
https://www.ncbi.nlm.nih.gov/pubmed/25007326
http://dx.doi.org/10.1371/journal.pone.0101470
_version_ 1782325207377117184
author Onoa, Bibiana
Schneider, Anna R.
Brooks, Matthew D.
Grob, Patricia
Nogales, Eva
Geissler, Phillip L.
Niyogi, Krishna K.
Bustamante, Carlos
author_facet Onoa, Bibiana
Schneider, Anna R.
Brooks, Matthew D.
Grob, Patricia
Nogales, Eva
Geissler, Phillip L.
Niyogi, Krishna K.
Bustamante, Carlos
author_sort Onoa, Bibiana
collection PubMed
description Photoautotrophic organisms efficiently regulate absorption of light energy to sustain photochemistry while promoting photoprotection. Photoprotection is achieved in part by triggering a series of dissipative processes termed non-photochemical quenching (NPQ), which depend on the re-organization of photosystem (PS) II supercomplexes in thylakoid membranes. Using atomic force microscopy, we characterized the structural attributes of grana thylakoids from Arabidopsis thaliana to correlate differences in PSII organization with the role of SOQ1, a recently discovered thylakoid protein that prevents formation of a slowly reversible NPQ state. We developed a statistical image analysis suite to discriminate disordered from crystalline particles and classify crystalline arrays according to their unit cell properties. Through detailed analysis of the local organization of PSII supercomplexes in ordered and disordered phases, we found evidence that interactions among light-harvesting antenna complexes are weakened in the absence of SOQ1, inducing protein rearrangements that favor larger separations between PSII complexes in the majority (disordered) phase and reshaping the PSII crystallization landscape. The features we observe are distinct from known protein rearrangements associated with NPQ, providing further support for a role of SOQ1 in a novel NPQ pathway. The particle clustering and unit cell methodology developed here is generalizable to multiple types of microscopy and will enable unbiased analysis and comparison of large data sets.
format Online
Article
Text
id pubmed-4090009
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-40900092014-07-14 Atomic Force Microscopy of Photosystem II and Its Unit Cell Clustering Quantitatively Delineate the Mesoscale Variability in Arabidopsis Thylakoids Onoa, Bibiana Schneider, Anna R. Brooks, Matthew D. Grob, Patricia Nogales, Eva Geissler, Phillip L. Niyogi, Krishna K. Bustamante, Carlos PLoS One Research Article Photoautotrophic organisms efficiently regulate absorption of light energy to sustain photochemistry while promoting photoprotection. Photoprotection is achieved in part by triggering a series of dissipative processes termed non-photochemical quenching (NPQ), which depend on the re-organization of photosystem (PS) II supercomplexes in thylakoid membranes. Using atomic force microscopy, we characterized the structural attributes of grana thylakoids from Arabidopsis thaliana to correlate differences in PSII organization with the role of SOQ1, a recently discovered thylakoid protein that prevents formation of a slowly reversible NPQ state. We developed a statistical image analysis suite to discriminate disordered from crystalline particles and classify crystalline arrays according to their unit cell properties. Through detailed analysis of the local organization of PSII supercomplexes in ordered and disordered phases, we found evidence that interactions among light-harvesting antenna complexes are weakened in the absence of SOQ1, inducing protein rearrangements that favor larger separations between PSII complexes in the majority (disordered) phase and reshaping the PSII crystallization landscape. The features we observe are distinct from known protein rearrangements associated with NPQ, providing further support for a role of SOQ1 in a novel NPQ pathway. The particle clustering and unit cell methodology developed here is generalizable to multiple types of microscopy and will enable unbiased analysis and comparison of large data sets. Public Library of Science 2014-07-09 /pmc/articles/PMC4090009/ /pubmed/25007326 http://dx.doi.org/10.1371/journal.pone.0101470 Text en © 2014 Onoa et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Onoa, Bibiana
Schneider, Anna R.
Brooks, Matthew D.
Grob, Patricia
Nogales, Eva
Geissler, Phillip L.
Niyogi, Krishna K.
Bustamante, Carlos
Atomic Force Microscopy of Photosystem II and Its Unit Cell Clustering Quantitatively Delineate the Mesoscale Variability in Arabidopsis Thylakoids
title Atomic Force Microscopy of Photosystem II and Its Unit Cell Clustering Quantitatively Delineate the Mesoscale Variability in Arabidopsis Thylakoids
title_full Atomic Force Microscopy of Photosystem II and Its Unit Cell Clustering Quantitatively Delineate the Mesoscale Variability in Arabidopsis Thylakoids
title_fullStr Atomic Force Microscopy of Photosystem II and Its Unit Cell Clustering Quantitatively Delineate the Mesoscale Variability in Arabidopsis Thylakoids
title_full_unstemmed Atomic Force Microscopy of Photosystem II and Its Unit Cell Clustering Quantitatively Delineate the Mesoscale Variability in Arabidopsis Thylakoids
title_short Atomic Force Microscopy of Photosystem II and Its Unit Cell Clustering Quantitatively Delineate the Mesoscale Variability in Arabidopsis Thylakoids
title_sort atomic force microscopy of photosystem ii and its unit cell clustering quantitatively delineate the mesoscale variability in arabidopsis thylakoids
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4090009/
https://www.ncbi.nlm.nih.gov/pubmed/25007326
http://dx.doi.org/10.1371/journal.pone.0101470
work_keys_str_mv AT onoabibiana atomicforcemicroscopyofphotosystemiianditsunitcellclusteringquantitativelydelineatethemesoscalevariabilityinarabidopsisthylakoids
AT schneiderannar atomicforcemicroscopyofphotosystemiianditsunitcellclusteringquantitativelydelineatethemesoscalevariabilityinarabidopsisthylakoids
AT brooksmatthewd atomicforcemicroscopyofphotosystemiianditsunitcellclusteringquantitativelydelineatethemesoscalevariabilityinarabidopsisthylakoids
AT grobpatricia atomicforcemicroscopyofphotosystemiianditsunitcellclusteringquantitativelydelineatethemesoscalevariabilityinarabidopsisthylakoids
AT nogaleseva atomicforcemicroscopyofphotosystemiianditsunitcellclusteringquantitativelydelineatethemesoscalevariabilityinarabidopsisthylakoids
AT geisslerphillipl atomicforcemicroscopyofphotosystemiianditsunitcellclusteringquantitativelydelineatethemesoscalevariabilityinarabidopsisthylakoids
AT niyogikrishnak atomicforcemicroscopyofphotosystemiianditsunitcellclusteringquantitativelydelineatethemesoscalevariabilityinarabidopsisthylakoids
AT bustamantecarlos atomicforcemicroscopyofphotosystemiianditsunitcellclusteringquantitativelydelineatethemesoscalevariabilityinarabidopsisthylakoids