Physical Features of Intracellular Proteins that Moonlight on the Cell Surface
Moonlighting proteins comprise a subset of multifunctional proteins that perform two or more biochemical functions that are not due to gene fusions, multiple splice variants, proteolytic fragments, or promiscuous enzyme activities. The project described herein focuses on a sub-set of moonlighting pr...
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description | Moonlighting proteins comprise a subset of multifunctional proteins that perform two or more biochemical functions that are not due to gene fusions, multiple splice variants, proteolytic fragments, or promiscuous enzyme activities. The project described herein focuses on a sub-set of moonlighting proteins that have a canonical biochemical function inside the cell and perform a second biochemical function on the cell surface in at least one species. The goal of this project is to consider the biophysical features of these moonlighting proteins to determine whether they have shared characteristics or defining features that might suggest why these particular proteins were adopted for a second function on the cell surface, or if these proteins resemble typical intracellular proteins. The latter might suggest that many other normally intracellular proteins found on the cell surface might also be moonlighting in this fashion. We have identified 30 types of proteins that have different functions inside the cell and on the cell surface. Some of these proteins are found to moonlight on the surface of multiple species, sometimes with different extracellular functions in different species, so there are a total of 98 proteins in the study set. Although a variety of intracellular proteins (enzymes, chaperones, etc.) are observed to be re-used on the cell surface, for the most part, these proteins were found to have physical characteristics typical of intracellular proteins. Many other intracellular proteins have also been found on the surface of bacterial pathogens and other organisms in proteomics experiments. It is quite possible that many of those proteins also have a moonlighting function on the cell surface. The increasing number and variety of known moonlighting proteins suggest that there may be more moonlighting proteins than previously thought, and moonlighting might be a common feature of many more proteins. |
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The project described herein focuses on a sub-set of moonlighting proteins that have a canonical biochemical function inside the cell and perform a second biochemical function on the cell surface in at least one species. The goal of this project is to consider the biophysical features of these moonlighting proteins to determine whether they have shared characteristics or defining features that might suggest why these particular proteins were adopted for a second function on the cell surface, or if these proteins resemble typical intracellular proteins. The latter might suggest that many other normally intracellular proteins found on the cell surface might also be moonlighting in this fashion. We have identified 30 types of proteins that have different functions inside the cell and on the cell surface. Some of these proteins are found to moonlight on the surface of multiple species, sometimes with different extracellular functions in different species, so there are a total of 98 proteins in the study set. Although a variety of intracellular proteins (enzymes, chaperones, etc.) are observed to be re-used on the cell surface, for the most part, these proteins were found to have physical characteristics typical of intracellular proteins. Many other intracellular proteins have also been found on the surface of bacterial pathogens and other organisms in proteomics experiments. It is quite possible that many of those proteins also have a moonlighting function on the cell surface. The increasing number and variety of known moonlighting proteins suggest that there may be more moonlighting proteins than previously thought, and moonlighting might be a common feature of many more proteins.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0130575</identifier><identifier>PMID: 26110848</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Alternative splicing ; Amino acids ; Bacterial Proteins - metabolism ; Binding sites ; Biochemistry ; Cell Membrane - metabolism ; Cell surface ; Chaperones ; Enzymatic activity ; Enzymes ; Genes ; Gram-positive bacteria ; Intracellular ; Membrane Proteins - metabolism ; Mycobacterium avium ; Physical characteristics ; Physical properties ; Protein Conformation ; Proteins ; Proteolysis ; Proteomics ; Species ; Streptococcus infections ; Streptococcus pneumoniae ; Trends</subject><ispartof>PloS one, 2015-06, Vol.10 (6), p.e0130575-e0130575</ispartof><rights>COPYRIGHT 2015 Public Library of Science</rights><rights>2015 Amblee, Jeffery. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2015 Amblee, Jeffery 2015 Amblee, Jeffery</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c692t-9c19369b88262cf8fdd6804ecf2cae829485fe182cd53721641a89dc0c5971c3</citedby><cites>FETCH-LOGICAL-c692t-9c19369b88262cf8fdd6804ecf2cae829485fe182cd53721641a89dc0c5971c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4481411/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4481411/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,2102,2928,23866,27924,27925,53791,53793,79600,79601</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26110848$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Pizarro, Juan Carlos</contributor><creatorcontrib>Amblee, Vaishak</creatorcontrib><creatorcontrib>Jeffery, Constance J</creatorcontrib><title>Physical Features of Intracellular Proteins that Moonlight on the Cell Surface</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Moonlighting proteins comprise a subset of multifunctional proteins that perform two or more biochemical functions that are not due to gene fusions, multiple splice variants, proteolytic fragments, or promiscuous enzyme activities. The project described herein focuses on a sub-set of moonlighting proteins that have a canonical biochemical function inside the cell and perform a second biochemical function on the cell surface in at least one species. The goal of this project is to consider the biophysical features of these moonlighting proteins to determine whether they have shared characteristics or defining features that might suggest why these particular proteins were adopted for a second function on the cell surface, or if these proteins resemble typical intracellular proteins. The latter might suggest that many other normally intracellular proteins found on the cell surface might also be moonlighting in this fashion. We have identified 30 types of proteins that have different functions inside the cell and on the cell surface. Some of these proteins are found to moonlight on the surface of multiple species, sometimes with different extracellular functions in different species, so there are a total of 98 proteins in the study set. Although a variety of intracellular proteins (enzymes, chaperones, etc.) are observed to be re-used on the cell surface, for the most part, these proteins were found to have physical characteristics typical of intracellular proteins. Many other intracellular proteins have also been found on the surface of bacterial pathogens and other organisms in proteomics experiments. It is quite possible that many of those proteins also have a moonlighting function on the cell surface. The increasing number and variety of known moonlighting proteins suggest that there may be more moonlighting proteins than previously thought, and moonlighting might be a common feature of many more proteins.</description><subject>Alternative splicing</subject><subject>Amino acids</subject><subject>Bacterial Proteins - metabolism</subject><subject>Binding sites</subject><subject>Biochemistry</subject><subject>Cell Membrane - metabolism</subject><subject>Cell surface</subject><subject>Chaperones</subject><subject>Enzymatic activity</subject><subject>Enzymes</subject><subject>Genes</subject><subject>Gram-positive bacteria</subject><subject>Intracellular</subject><subject>Membrane Proteins - metabolism</subject><subject>Mycobacterium avium</subject><subject>Physical characteristics</subject><subject>Physical properties</subject><subject>Protein Conformation</subject><subject>Proteins</subject><subject>Proteolysis</subject><subject>Proteomics</subject><subject>Species</subject><subject>Streptococcus infections</subject><subject>Streptococcus pneumoniae</subject><subject>Trends</subject><issn>1932-6203</issn><issn>1932-6203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>DOA</sourceid><recordid>eNqNkl1v0zAUhiMEYmPwDxBEQkJw0eKPxLFvkKZqg0qDTWzi1nL90bhy42I7aPv3ODSbGrQL5ItYJ895ffz6LYrXEMwhbuCnje9DJ9x85zs9BxCDuqmfFMeQYTQjCOCnB_uj4kWMGwBqTAl5XhwhAiGgFT0uvl-1d9FK4cpzLVIfdCy9KZddCkJq53onQnkVfNK2i2VqRSq_ed85u25T6btc0eUic-V1H0zueFk8M8JF_Wr8nhQ352c3i6-zi8svy8XpxUwShtKMyTwaYStKEUHSUKMUoaDS0iApNEWsorXRkCKpatwgSCooKFMSyJo1UOKT4u1edud85KMTkUPCIGpIjWEmlntCebHhu2C3ItxxLyz_W_BhzUVIVjrNmcaCEUQMFaQSAlOMsDIGMbhSaqVB1vo8ntavtlpJPbjjJqLTP51t-dr_5lVFYQWHYT6MAsH_6nVMfGvjYK_otO_3cxMAGRvQd_-gj99upNYiX8B2xg_vNYjy0ypbWzeorjM1f4TKS-mtlTk2xub6pOHjpCEzSd-mtehj5MvrH__PXv6csu8P2FYLl9roXZ-s7-IUrPagDD7GoM2DyRDwIfX3bvAh9XxMfW57c_hAD033Mcd_ALWs-80</recordid><startdate>20150625</startdate><enddate>20150625</enddate><creator>Amblee, Vaishak</creator><creator>Jeffery, Constance J</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QO</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TG</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>KB0</scope><scope>KL.</scope><scope>L6V</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20150625</creationdate><title>Physical Features of Intracellular Proteins that Moonlight on the Cell Surface</title><author>Amblee, Vaishak ; Jeffery, Constance J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c692t-9c19369b88262cf8fdd6804ecf2cae829485fe182cd53721641a89dc0c5971c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Alternative splicing</topic><topic>Amino acids</topic><topic>Bacterial Proteins - metabolism</topic><topic>Binding sites</topic><topic>Biochemistry</topic><topic>Cell Membrane - metabolism</topic><topic>Cell surface</topic><topic>Chaperones</topic><topic>Enzymatic activity</topic><topic>Enzymes</topic><topic>Genes</topic><topic>Gram-positive bacteria</topic><topic>Intracellular</topic><topic>Membrane Proteins - metabolism</topic><topic>Mycobacterium avium</topic><topic>Physical characteristics</topic><topic>Physical properties</topic><topic>Protein Conformation</topic><topic>Proteins</topic><topic>Proteolysis</topic><topic>Proteomics</topic><topic>Species</topic><topic>Streptococcus infections</topic><topic>Streptococcus pneumoniae</topic><topic>Trends</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Amblee, Vaishak</creatorcontrib><creatorcontrib>Jeffery, Constance J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology 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>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Materials Science Database</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Meteorological & Geoastrophysical Abstracts - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PloS one</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Amblee, Vaishak</au><au>Jeffery, Constance J</au><au>Pizarro, Juan Carlos</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Physical Features of Intracellular Proteins that Moonlight on the Cell Surface</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2015-06-25</date><risdate>2015</risdate><volume>10</volume><issue>6</issue><spage>e0130575</spage><epage>e0130575</epage><pages>e0130575-e0130575</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Moonlighting proteins comprise a subset of multifunctional proteins that perform two or more biochemical functions that are not due to gene fusions, multiple splice variants, proteolytic fragments, or promiscuous enzyme activities. The project described herein focuses on a sub-set of moonlighting proteins that have a canonical biochemical function inside the cell and perform a second biochemical function on the cell surface in at least one species. The goal of this project is to consider the biophysical features of these moonlighting proteins to determine whether they have shared characteristics or defining features that might suggest why these particular proteins were adopted for a second function on the cell surface, or if these proteins resemble typical intracellular proteins. The latter might suggest that many other normally intracellular proteins found on the cell surface might also be moonlighting in this fashion. We have identified 30 types of proteins that have different functions inside the cell and on the cell surface. Some of these proteins are found to moonlight on the surface of multiple species, sometimes with different extracellular functions in different species, so there are a total of 98 proteins in the study set. Although a variety of intracellular proteins (enzymes, chaperones, etc.) are observed to be re-used on the cell surface, for the most part, these proteins were found to have physical characteristics typical of intracellular proteins. Many other intracellular proteins have also been found on the surface of bacterial pathogens and other organisms in proteomics experiments. It is quite possible that many of those proteins also have a moonlighting function on the cell surface. The increasing number and variety of known moonlighting proteins suggest that there may be more moonlighting proteins than previously thought, and moonlighting might be a common feature of many more proteins.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>26110848</pmid><doi>10.1371/journal.pone.0130575</doi><oa>free_for_read</oa></addata></record> |
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subjects | Alternative splicing Amino acids Bacterial Proteins - metabolism Binding sites Biochemistry Cell Membrane - metabolism Cell surface Chaperones Enzymatic activity Enzymes Genes Gram-positive bacteria Intracellular Membrane Proteins - metabolism Mycobacterium avium Physical characteristics Physical properties Protein Conformation Proteins Proteolysis Proteomics Species Streptococcus infections Streptococcus pneumoniae Trends |
title | Physical Features of Intracellular Proteins that Moonlight on the Cell Surface |
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