Identification of a Natural Green Light Absorbing Chloride Conducting Channelrhodopsin from Proteomonas sulcata
Chloride conducting channelrhodopsins (ChloCs) are new members of the optogenetic toolbox that enable neuronal inhibition in target cells. Originally, ChloCs have been engineered from cation conducting channelrhodopsins (ChRs), and later identified in a cryptophyte alga genome. We noticed that the s...
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Veröffentlicht in: | The Journal of biological chemistry 2016-02, Vol.291 (8), p.4121-4127 |
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description | Chloride conducting channelrhodopsins (ChloCs) are new members of the optogenetic toolbox that enable neuronal inhibition in target cells. Originally, ChloCs have been engineered from cation conducting channelrhodopsins (ChRs), and later identified in a cryptophyte alga genome. We noticed that the sequence of a previously described Proteomonas sulcata ChR (PsChR1) was highly homologous to the naturally occurring and previously reported ChloCs GtACR1/2, but was not recognized as an anion conducting channel. Based on electrophysiological measurements obtained under various ionic conditions, we concluded that the PsChR1 photocurrent at physiological conditions is strongly inward rectifying and predominantly carried by chloride. The maximum activation was noted at excitation with light of 540 nm. An initial spectroscopic characterization of purified protein revealed that the photocycle and the transport mechanism of PsChR1 differ significantly from cation conducting ChRs. Hence, we concluded that PsChR1 is an anion conducting ChR, now renamed PsACR1, with a red-shifted absorption suited for multicolor optogenetic experiments in combination with blue light absorbing cation conducting ChRs. |
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Originally, ChloCs have been engineered from cation conducting channelrhodopsins (ChRs), and later identified in a cryptophyte alga genome. We noticed that the sequence of a previously described Proteomonas sulcata ChR (PsChR1) was highly homologous to the naturally occurring and previously reported ChloCs GtACR1/2, but was not recognized as an anion conducting channel. Based on electrophysiological measurements obtained under various ionic conditions, we concluded that the PsChR1 photocurrent at physiological conditions is strongly inward rectifying and predominantly carried by chloride. The maximum activation was noted at excitation with light of 540 nm. An initial spectroscopic characterization of purified protein revealed that the photocycle and the transport mechanism of PsChR1 differ significantly from cation conducting ChRs. Hence, we concluded that PsChR1 is an anion conducting ChR, now renamed PsACR1, with a red-shifted absorption suited for multicolor optogenetic experiments in combination with blue light absorbing cation conducting ChRs.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1074/jbc.M115.699637</identifier><identifier>PMID: 26740624</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>algae ; biophysics ; channelrhodopsin ; chloride channel ; Chloride Channels - chemistry ; Chloride Channels - genetics ; Chloride Channels - metabolism ; Cryptophyta - chemistry ; Cryptophyta - genetics ; Cryptophyta - metabolism ; electrophysiology ; Ion Transport - physiology ; Light ; Molecular Biophysics ; optogenetics ; patch clamp ; photobiology ; Rhodopsin - chemistry ; Rhodopsin - genetics ; Rhodopsin - metabolism ; ultraviolet-visible spectroscopy (UV-Vis spectroscopy)</subject><ispartof>The Journal of biological chemistry, 2016-02, Vol.291 (8), p.4121-4127</ispartof><rights>2016 © 2016 ASBMB. Currently published by Elsevier Inc; originally published by American Society for Biochemistry and Molecular Biology.</rights><rights>2016 by The American Society for Biochemistry and Molecular Biology, Inc.</rights><rights>2016 by The American Society for Biochemistry and Molecular Biology, Inc. 2016 The American Society for Biochemistry and Molecular Biology, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c555t-9b638ce89e2398ffbfcb0e0715bac4f4497a88b1e13a12f07318bbc010f447a73</citedby><cites>FETCH-LOGICAL-c555t-9b638ce89e2398ffbfcb0e0715bac4f4497a88b1e13a12f07318bbc010f447a73</cites><orcidid>0000-0002-8079-7042</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4759187/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4759187/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26740624$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wietek, Jonas</creatorcontrib><creatorcontrib>Broser, Matthias</creatorcontrib><creatorcontrib>Krause, Benjamin S.</creatorcontrib><creatorcontrib>Hegemann, Peter</creatorcontrib><title>Identification of a Natural Green Light Absorbing Chloride Conducting Channelrhodopsin from Proteomonas sulcata</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><description>Chloride conducting channelrhodopsins (ChloCs) are new members of the optogenetic toolbox that enable neuronal inhibition in target cells. Originally, ChloCs have been engineered from cation conducting channelrhodopsins (ChRs), and later identified in a cryptophyte alga genome. We noticed that the sequence of a previously described Proteomonas sulcata ChR (PsChR1) was highly homologous to the naturally occurring and previously reported ChloCs GtACR1/2, but was not recognized as an anion conducting channel. Based on electrophysiological measurements obtained under various ionic conditions, we concluded that the PsChR1 photocurrent at physiological conditions is strongly inward rectifying and predominantly carried by chloride. The maximum activation was noted at excitation with light of 540 nm. An initial spectroscopic characterization of purified protein revealed that the photocycle and the transport mechanism of PsChR1 differ significantly from cation conducting ChRs. Hence, we concluded that PsChR1 is an anion conducting ChR, now renamed PsACR1, with a red-shifted absorption suited for multicolor optogenetic experiments in combination with blue light absorbing cation conducting ChRs.</description><subject>algae</subject><subject>biophysics</subject><subject>channelrhodopsin</subject><subject>chloride channel</subject><subject>Chloride Channels - chemistry</subject><subject>Chloride Channels - genetics</subject><subject>Chloride Channels - metabolism</subject><subject>Cryptophyta - chemistry</subject><subject>Cryptophyta - genetics</subject><subject>Cryptophyta - metabolism</subject><subject>electrophysiology</subject><subject>Ion Transport - physiology</subject><subject>Light</subject><subject>Molecular Biophysics</subject><subject>optogenetics</subject><subject>patch clamp</subject><subject>photobiology</subject><subject>Rhodopsin - chemistry</subject><subject>Rhodopsin - genetics</subject><subject>Rhodopsin - metabolism</subject><subject>ultraviolet-visible spectroscopy (UV-Vis spectroscopy)</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kc9vFCEUx4nR2LV69mY4epktzAwDXEyajdYm64-DJt4IMI9dmhlYgWnify-bqY0e5ELC-_B9PD4IvaZkSwnvr-6M3X6ilG0HKYeOP0EbSkTXdIz-eIo2hLS0kS0TF-hFznekrl7S5-iiHXhPhrbfoHg7QijeeauLjwFHhzX-rMuS9IRvEkDAe384FnxtckzGhwPeHaeY_Ah4F8O42LKe6RBgSsc4xlP2AbsUZ_w1xQJxjkFnnJepttAv0TOnpwyvHvZL9P3D-2-7j83-y83t7nrfWMZYaaQZOmFBSGg7KZwzzhoChFNmtO1d30uuhTAUaKdp6wjvqDDGEkpqjWveXaJ3a-5pMTOMtg5ZJ1Kn5Gedfqmovfq3EvxRHeK96jmTVJwD3j4EpPhzgVzU7LOFadIB4pIV5QMng-iYqOjVitoUc07gHttQos6aVNWkzprUqqneePP36x75P14qIFcA6h_de0gqWw_BwugT2KLG6P8b_hvCt6Tf</recordid><startdate>20160219</startdate><enddate>20160219</enddate><creator>Wietek, Jonas</creator><creator>Broser, Matthias</creator><creator>Krause, Benjamin S.</creator><creator>Hegemann, Peter</creator><general>Elsevier Inc</general><general>American Society for Biochemistry and Molecular Biology</general><scope>6I.</scope><scope>AAFTH</scope><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>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-8079-7042</orcidid></search><sort><creationdate>20160219</creationdate><title>Identification of a Natural Green Light Absorbing Chloride Conducting Channelrhodopsin from Proteomonas sulcata</title><author>Wietek, Jonas ; Broser, Matthias ; Krause, Benjamin S. ; Hegemann, Peter</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c555t-9b638ce89e2398ffbfcb0e0715bac4f4497a88b1e13a12f07318bbc010f447a73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>algae</topic><topic>biophysics</topic><topic>channelrhodopsin</topic><topic>chloride channel</topic><topic>Chloride Channels - chemistry</topic><topic>Chloride Channels - genetics</topic><topic>Chloride Channels - metabolism</topic><topic>Cryptophyta - chemistry</topic><topic>Cryptophyta - genetics</topic><topic>Cryptophyta - metabolism</topic><topic>electrophysiology</topic><topic>Ion Transport - physiology</topic><topic>Light</topic><topic>Molecular Biophysics</topic><topic>optogenetics</topic><topic>patch clamp</topic><topic>photobiology</topic><topic>Rhodopsin - chemistry</topic><topic>Rhodopsin - genetics</topic><topic>Rhodopsin - metabolism</topic><topic>ultraviolet-visible spectroscopy (UV-Vis spectroscopy)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wietek, Jonas</creatorcontrib><creatorcontrib>Broser, Matthias</creatorcontrib><creatorcontrib>Krause, Benjamin S.</creatorcontrib><creatorcontrib>Hegemann, Peter</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wietek, Jonas</au><au>Broser, Matthias</au><au>Krause, Benjamin S.</au><au>Hegemann, Peter</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of a Natural Green Light Absorbing Chloride Conducting Channelrhodopsin from Proteomonas sulcata</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>2016-02-19</date><risdate>2016</risdate><volume>291</volume><issue>8</issue><spage>4121</spage><epage>4127</epage><pages>4121-4127</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><abstract>Chloride conducting channelrhodopsins (ChloCs) are new members of the optogenetic toolbox that enable neuronal inhibition in target cells. Originally, ChloCs have been engineered from cation conducting channelrhodopsins (ChRs), and later identified in a cryptophyte alga genome. We noticed that the sequence of a previously described Proteomonas sulcata ChR (PsChR1) was highly homologous to the naturally occurring and previously reported ChloCs GtACR1/2, but was not recognized as an anion conducting channel. Based on electrophysiological measurements obtained under various ionic conditions, we concluded that the PsChR1 photocurrent at physiological conditions is strongly inward rectifying and predominantly carried by chloride. The maximum activation was noted at excitation with light of 540 nm. An initial spectroscopic characterization of purified protein revealed that the photocycle and the transport mechanism of PsChR1 differ significantly from cation conducting ChRs. Hence, we concluded that PsChR1 is an anion conducting ChR, now renamed PsACR1, with a red-shifted absorption suited for multicolor optogenetic experiments in combination with blue light absorbing cation conducting ChRs.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>26740624</pmid><doi>10.1074/jbc.M115.699637</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-8079-7042</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | algae biophysics channelrhodopsin chloride channel Chloride Channels - chemistry Chloride Channels - genetics Chloride Channels - metabolism Cryptophyta - chemistry Cryptophyta - genetics Cryptophyta - metabolism electrophysiology Ion Transport - physiology Light Molecular Biophysics optogenetics patch clamp photobiology Rhodopsin - chemistry Rhodopsin - genetics Rhodopsin - metabolism ultraviolet-visible spectroscopy (UV-Vis spectroscopy) |
title | Identification of a Natural Green Light Absorbing Chloride Conducting Channelrhodopsin from Proteomonas sulcata |
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