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Proximity-based proteomics reveals the thylakoid lumen proteome in the cyanobacterium Synechococcus sp. PCC 7002
Cyanobacteria possess unique intracellular organization. Many proteomic studies have examined different features of cyanobacteria to learn about the intracellular structures and their respective functions. While these studies have made great progress in understanding cyanobacterial physiology, the c...
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Published in: | Photosynthesis research 2021-02, Vol.147 (2), p.177-195 |
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description | Cyanobacteria possess unique intracellular organization. Many proteomic studies have examined different features of cyanobacteria to learn about the intracellular structures and their respective functions. While these studies have made great progress in understanding cyanobacterial physiology, the conventional fractionation methods used to purify cellular structures have limitations; specifically, certain regions of cells cannot be purified with existing fractionation methods. Proximity-based proteomics techniques were developed to overcome the limitations of biochemical fractionation for proteomics. Proximity-based proteomics relies on spatiotemporal protein labeling followed by mass spectrometry of the labeled proteins to determine the proteome of the region of interest. We performed proximity-based proteomics in the cyanobacterium
Synechococcus
sp. PCC 7002 with the APEX2 enzyme, an engineered ascorbate peroxidase. We determined the proteome of the thylakoid lumen, a region of the cell that has remained challenging to study with existing methods, using a translational fusion between APEX2 and PsbU, a lumenal subunit of photosystem II. Our results demonstrate the power of APEX2 as a tool to study the cell biology of intracellular features and processes, including photosystem II assembly in cyanobacteria, with enhanced spatiotemporal resolution. |
doi_str_mv | 10.1007/s11120-020-00806-y |
format | article |
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Synechococcus
sp. PCC 7002 with the APEX2 enzyme, an engineered ascorbate peroxidase. We determined the proteome of the thylakoid lumen, a region of the cell that has remained challenging to study with existing methods, using a translational fusion between APEX2 and PsbU, a lumenal subunit of photosystem II. Our results demonstrate the power of APEX2 as a tool to study the cell biology of intracellular features and processes, including photosystem II assembly in cyanobacteria, with enhanced spatiotemporal resolution.</description><identifier>ISSN: 0166-8595</identifier><identifier>EISSN: 1573-5079</identifier><identifier>DOI: 10.1007/s11120-020-00806-y</identifier><identifier>PMID: 33280076</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>APEX2 ; Ascorbic acid ; B cells ; BASIC BIOLOGICAL SCIENCES ; Biochemistry ; Biomedical and Life Sciences ; Cyanobacteria ; Intracellular ; L-Ascorbate peroxidase ; Life Sciences ; Mass spectrometry ; Mass spectroscopy ; Original ; Original Article ; photosynthesis ; Photosystem II ; Physiological aspects ; Plant Genetics and Genomics ; Plant Physiology ; Plant Sciences ; Proteins ; Proteomes ; Proteomics ; proximity-based proteomics ; Synechococcus ; thylakoid lumen</subject><ispartof>Photosynthesis research, 2021-02, Vol.147 (2), p.177-195</ispartof><rights>The Author(s) 2020</rights><rights>COPYRIGHT 2021 Springer</rights><rights>The Author(s) 2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c574t-5357618583e8c05c109c03bdff242a7c9de88b027f05573b567b7469238b84983</citedby><cites>FETCH-LOGICAL-c574t-5357618583e8c05c109c03bdff242a7c9de88b027f05573b567b7469238b84983</cites><orcidid>0000-0002-6630-8345 ; 0000000266308345</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33280076$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/1734387$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Dahlgren, Kelsey K.</creatorcontrib><creatorcontrib>Gates, Colin</creatorcontrib><creatorcontrib>Lee, Thomas</creatorcontrib><creatorcontrib>Cameron, Jeffrey C.</creatorcontrib><creatorcontrib>National Renewable Energy Laboratory (NREL), Golden, CO (United States)</creatorcontrib><title>Proximity-based proteomics reveals the thylakoid lumen proteome in the cyanobacterium Synechococcus sp. PCC 7002</title><title>Photosynthesis research</title><addtitle>Photosynth Res</addtitle><addtitle>Photosynth Res</addtitle><description>Cyanobacteria possess unique intracellular organization. Many proteomic studies have examined different features of cyanobacteria to learn about the intracellular structures and their respective functions. While these studies have made great progress in understanding cyanobacterial physiology, the conventional fractionation methods used to purify cellular structures have limitations; specifically, certain regions of cells cannot be purified with existing fractionation methods. Proximity-based proteomics techniques were developed to overcome the limitations of biochemical fractionation for proteomics. Proximity-based proteomics relies on spatiotemporal protein labeling followed by mass spectrometry of the labeled proteins to determine the proteome of the region of interest. We performed proximity-based proteomics in the cyanobacterium
Synechococcus
sp. PCC 7002 with the APEX2 enzyme, an engineered ascorbate peroxidase. We determined the proteome of the thylakoid lumen, a region of the cell that has remained challenging to study with existing methods, using a translational fusion between APEX2 and PsbU, a lumenal subunit of photosystem II. 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PCC 7002</title><author>Dahlgren, Kelsey K. ; Gates, Colin ; Lee, Thomas ; Cameron, Jeffrey C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c574t-5357618583e8c05c109c03bdff242a7c9de88b027f05573b567b7469238b84983</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>APEX2</topic><topic>Ascorbic acid</topic><topic>B cells</topic><topic>BASIC BIOLOGICAL SCIENCES</topic><topic>Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Cyanobacteria</topic><topic>Intracellular</topic><topic>L-Ascorbate peroxidase</topic><topic>Life Sciences</topic><topic>Mass spectrometry</topic><topic>Mass spectroscopy</topic><topic>Original</topic><topic>Original Article</topic><topic>photosynthesis</topic><topic>Photosystem II</topic><topic>Physiological aspects</topic><topic>Plant Genetics and Genomics</topic><topic>Plant Physiology</topic><topic>Plant Sciences</topic><topic>Proteins</topic><topic>Proteomes</topic><topic>Proteomics</topic><topic>proximity-based proteomics</topic><topic>Synechococcus</topic><topic>thylakoid lumen</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dahlgren, Kelsey K.</creatorcontrib><creatorcontrib>Gates, Colin</creatorcontrib><creatorcontrib>Lee, Thomas</creatorcontrib><creatorcontrib>Cameron, Jeffrey C.</creatorcontrib><creatorcontrib>National Renewable Energy Laboratory (NREL), Golden, CO (United States)</creatorcontrib><collection>SpringerOpen</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>ProQuest_Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest Science Journals</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>OSTI.GOV</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Photosynthesis research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dahlgren, Kelsey K.</au><au>Gates, Colin</au><au>Lee, Thomas</au><au>Cameron, Jeffrey C.</au><aucorp>National Renewable Energy Laboratory (NREL), Golden, CO (United States)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Proximity-based proteomics reveals the thylakoid lumen proteome in the cyanobacterium Synechococcus sp. PCC 7002</atitle><jtitle>Photosynthesis research</jtitle><stitle>Photosynth Res</stitle><addtitle>Photosynth Res</addtitle><date>2021-02-01</date><risdate>2021</risdate><volume>147</volume><issue>2</issue><spage>177</spage><epage>195</epage><pages>177-195</pages><issn>0166-8595</issn><eissn>1573-5079</eissn><abstract>Cyanobacteria possess unique intracellular organization. Many proteomic studies have examined different features of cyanobacteria to learn about the intracellular structures and their respective functions. While these studies have made great progress in understanding cyanobacterial physiology, the conventional fractionation methods used to purify cellular structures have limitations; specifically, certain regions of cells cannot be purified with existing fractionation methods. Proximity-based proteomics techniques were developed to overcome the limitations of biochemical fractionation for proteomics. Proximity-based proteomics relies on spatiotemporal protein labeling followed by mass spectrometry of the labeled proteins to determine the proteome of the region of interest. We performed proximity-based proteomics in the cyanobacterium
Synechococcus
sp. PCC 7002 with the APEX2 enzyme, an engineered ascorbate peroxidase. We determined the proteome of the thylakoid lumen, a region of the cell that has remained challenging to study with existing methods, using a translational fusion between APEX2 and PsbU, a lumenal subunit of photosystem II. Our results demonstrate the power of APEX2 as a tool to study the cell biology of intracellular features and processes, including photosystem II assembly in cyanobacteria, with enhanced spatiotemporal resolution.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><pmid>33280076</pmid><doi>10.1007/s11120-020-00806-y</doi><tpages>19</tpages><orcidid>https://orcid.org/0000-0002-6630-8345</orcidid><orcidid>https://orcid.org/0000000266308345</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | APEX2 Ascorbic acid B cells BASIC BIOLOGICAL SCIENCES Biochemistry Biomedical and Life Sciences Cyanobacteria Intracellular L-Ascorbate peroxidase Life Sciences Mass spectrometry Mass spectroscopy Original Original Article photosynthesis Photosystem II Physiological aspects Plant Genetics and Genomics Plant Physiology Plant Sciences Proteins Proteomes Proteomics proximity-based proteomics Synechococcus thylakoid lumen |
title | Proximity-based proteomics reveals the thylakoid lumen proteome in the cyanobacterium Synechococcus sp. PCC 7002 |
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