Ultrasensitive fluorescent proteins for imaging neuronal activity
Fluorescent calcium sensors are widely used to image neural activity. Using structure-based mutagenesis and neuron-based screening, we developed a family of ultrasensitive protein calcium sensors (GCaMP6) that outperformed other sensors in cultured neurons and in zebrafish, flies and mice in vivo ....
Gespeichert in:
Veröffentlicht in: | Nature (London) 2013-07, Vol.499 (7458), p.295-300 |
---|---|
Hauptverfasser: | , , , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 300 |
---|---|
container_issue | 7458 |
container_start_page | 295 |
container_title | Nature (London) |
container_volume | 499 |
creator | Chen, Tsai-Wen Wardill, Trevor J. Sun, Yi Pulver, Stefan R. Renninger, Sabine L. Baohan, Amy Schreiter, Eric R. Kerr, Rex A. Orger, Michael B. Jayaraman, Vivek Looger, Loren L. Svoboda, Karel Kim, Douglas S. |
description | Fluorescent calcium sensors are widely used to image neural activity. Using structure-based mutagenesis and neuron-based screening, we developed a family of ultrasensitive protein calcium sensors (GCaMP6) that outperformed other sensors in cultured neurons and in zebrafish, flies and mice
in vivo
. In layer 2/3 pyramidal neurons of the mouse visual cortex, GCaMP6 reliably detected single action potentials in neuronal somata and orientation-tuned synaptic calcium transients in individual dendritic spines. The orientation tuning of structurally persistent spines was largely stable over timescales of weeks. Orientation tuning averaged across spine populations predicted the tuning of their parent cell. Although the somata of GABAergic neurons showed little orientation tuning, their dendrites included highly tuned dendritic segments (5–40-µm long). GCaMP6 sensors thus provide new windows into the organization and dynamics of neural circuits over multiple spatial and temporal scales.
Sensitive protein sensors of calcium have been created; these new tools are shown to report neural activity in cultured neurons, flies and zebrafish and can detect single action potentials and synaptic activation in the mouse visual cortex
in vivo
.
A new sensor for neural activity
Genetically encoded calcium sensors have brought neuronal recording to the tiny brains of invertebrates, but the methodology has lagged behind classical electrophysiology in vertebrates. Now Douglas Kim and colleagues have used selective mutagenesis to engineer a new ultrasensitive probe, GCaMP6, demonstrating improved spatial and temporal resolution
in vivo
, from flies to zebrafish. In addition, in mouse visual cortex GCaMP6 can reliably detect single action potentials and single-spine orientation tuning. GCaMP6 sensors can be used to image large groups of neurons as well as tiny synaptic compartments over multiple imaging sessions separated by months, offering a flexible new tool for brain research and calcium signalling studies. |
doi_str_mv | 10.1038/nature12354 |
format | Article |
fullrecord | <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_1668271405</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A337370689</galeid><sourcerecordid>A337370689</sourcerecordid><originalsourceid>FETCH-LOGICAL-c656t-4da3f6079af25217d8c735f6d371858ec650a0b12cf5d4004b779289c9c3f4593</originalsourceid><addsrcrecordid>eNp10s1rFDEUAPBBFFurJ-8yWARFp-Y7meOy-FEoCtriMWQzL0PKbGabZMT-92bpandlJIdA8st7L8mrqucYnWFE1ftg8hQBE8rZg-oYMykaJpR8WB0jRFSDFBVH1ZOUrhFCHEv2uDoiVAlFuDquFldDjiZBSD77n1C7YRojJAsh15s4ZvAh1W6MtV-b3oe-DjDFMZihNrYc8Pn2afXImSHBs918Ul19_HC5_NxcfP10vlxcNFZwkRvWGeoEkq1xhBMsO2Ul5U50VGLFFRSFDFphYh3vGEJsJWVLVGtbSx3jLT2pXt_FLWXdTJCyXvtS5zCYAOOUNBblShIzxAs9_Ydej1MsRRfFcMsQYYTdq94MoH1wY3kJuw2qF5RKKpFQ27TNjOohQDTDGMD5snzgX854u_E3eh-dzaAyOlh7Oxv1zcGBYjL8yr2ZUtLn378d2rf_t4vLH8svs9rGMaUITm9i-et4qzHS2_7Se_1V9Ivdy06rNXR_7Z-GKuDVDphkzeCiCdaneycFagWjxb27c6lshR7i3hfN5P0NTBHiJA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1419402424</pqid></control><display><type>article</type><title>Ultrasensitive fluorescent proteins for imaging neuronal activity</title><source>MEDLINE</source><source>SpringerLink Journals</source><source>Nature Journals Online</source><creator>Chen, Tsai-Wen ; Wardill, Trevor J. ; Sun, Yi ; Pulver, Stefan R. ; Renninger, Sabine L. ; Baohan, Amy ; Schreiter, Eric R. ; Kerr, Rex A. ; Orger, Michael B. ; Jayaraman, Vivek ; Looger, Loren L. ; Svoboda, Karel ; Kim, Douglas S.</creator><creatorcontrib>Chen, Tsai-Wen ; Wardill, Trevor J. ; Sun, Yi ; Pulver, Stefan R. ; Renninger, Sabine L. ; Baohan, Amy ; Schreiter, Eric R. ; Kerr, Rex A. ; Orger, Michael B. ; Jayaraman, Vivek ; Looger, Loren L. ; Svoboda, Karel ; Kim, Douglas S.</creatorcontrib><description>Fluorescent calcium sensors are widely used to image neural activity. Using structure-based mutagenesis and neuron-based screening, we developed a family of ultrasensitive protein calcium sensors (GCaMP6) that outperformed other sensors in cultured neurons and in zebrafish, flies and mice
in vivo
. In layer 2/3 pyramidal neurons of the mouse visual cortex, GCaMP6 reliably detected single action potentials in neuronal somata and orientation-tuned synaptic calcium transients in individual dendritic spines. The orientation tuning of structurally persistent spines was largely stable over timescales of weeks. Orientation tuning averaged across spine populations predicted the tuning of their parent cell. Although the somata of GABAergic neurons showed little orientation tuning, their dendrites included highly tuned dendritic segments (5–40-µm long). GCaMP6 sensors thus provide new windows into the organization and dynamics of neural circuits over multiple spatial and temporal scales.
Sensitive protein sensors of calcium have been created; these new tools are shown to report neural activity in cultured neurons, flies and zebrafish and can detect single action potentials and synaptic activation in the mouse visual cortex
in vivo
.
A new sensor for neural activity
Genetically encoded calcium sensors have brought neuronal recording to the tiny brains of invertebrates, but the methodology has lagged behind classical electrophysiology in vertebrates. Now Douglas Kim and colleagues have used selective mutagenesis to engineer a new ultrasensitive probe, GCaMP6, demonstrating improved spatial and temporal resolution
in vivo
, from flies to zebrafish. In addition, in mouse visual cortex GCaMP6 can reliably detect single action potentials and single-spine orientation tuning. GCaMP6 sensors can be used to image large groups of neurons as well as tiny synaptic compartments over multiple imaging sessions separated by months, offering a flexible new tool for brain research and calcium signalling studies.</description><identifier>ISSN: 0028-0836</identifier><identifier>EISSN: 1476-4687</identifier><identifier>DOI: 10.1038/nature12354</identifier><identifier>PMID: 23868258</identifier><identifier>CODEN: NATUAS</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>631/1647/1888/2249 ; Action Potentials ; Animals ; Biological and medical sciences ; Calcium - metabolism ; Calcium-Binding Proteins - chemistry ; Calcium-Binding Proteins - genetics ; Cells, Cultured ; Danio rerio ; Dendritic Spines - metabolism ; Eye and associated structures. Visual pathways and centers. Vision ; Fluorescent Dyes - chemistry ; Fluorescent proteins ; Fundamental and applied biological sciences. Psychology ; GABAergic Neurons - metabolism ; Humanities and Social Sciences ; Insects ; Luminescent Proteins - chemistry ; Luminescent Proteins - genetics ; Mice ; Molecular Imaging ; multidisciplinary ; Mutagenesis ; Mutation ; Neuroimaging ; Neurology ; Neurons ; Properties ; Protein Engineering ; Proteins ; Pyramidal Cells - metabolism ; Pyramidal Cells - physiology ; Science ; Sensors ; Spine ; Vertebrates: nervous system and sense organs ; Visual Cortex - cytology ; Visual Cortex - physiology</subject><ispartof>Nature (London), 2013-07, Vol.499 (7458), p.295-300</ispartof><rights>Springer Nature Limited 2013</rights><rights>2014 INIST-CNRS</rights><rights>COPYRIGHT 2013 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Jul 18, 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c656t-4da3f6079af25217d8c735f6d371858ec650a0b12cf5d4004b779289c9c3f4593</citedby><cites>FETCH-LOGICAL-c656t-4da3f6079af25217d8c735f6d371858ec650a0b12cf5d4004b779289c9c3f4593</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/nature12354$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/nature12354$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=27609643$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23868258$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Tsai-Wen</creatorcontrib><creatorcontrib>Wardill, Trevor J.</creatorcontrib><creatorcontrib>Sun, Yi</creatorcontrib><creatorcontrib>Pulver, Stefan R.</creatorcontrib><creatorcontrib>Renninger, Sabine L.</creatorcontrib><creatorcontrib>Baohan, Amy</creatorcontrib><creatorcontrib>Schreiter, Eric R.</creatorcontrib><creatorcontrib>Kerr, Rex A.</creatorcontrib><creatorcontrib>Orger, Michael B.</creatorcontrib><creatorcontrib>Jayaraman, Vivek</creatorcontrib><creatorcontrib>Looger, Loren L.</creatorcontrib><creatorcontrib>Svoboda, Karel</creatorcontrib><creatorcontrib>Kim, Douglas S.</creatorcontrib><title>Ultrasensitive fluorescent proteins for imaging neuronal activity</title><title>Nature (London)</title><addtitle>Nature</addtitle><addtitle>Nature</addtitle><description>Fluorescent calcium sensors are widely used to image neural activity. Using structure-based mutagenesis and neuron-based screening, we developed a family of ultrasensitive protein calcium sensors (GCaMP6) that outperformed other sensors in cultured neurons and in zebrafish, flies and mice
in vivo
. In layer 2/3 pyramidal neurons of the mouse visual cortex, GCaMP6 reliably detected single action potentials in neuronal somata and orientation-tuned synaptic calcium transients in individual dendritic spines. The orientation tuning of structurally persistent spines was largely stable over timescales of weeks. Orientation tuning averaged across spine populations predicted the tuning of their parent cell. Although the somata of GABAergic neurons showed little orientation tuning, their dendrites included highly tuned dendritic segments (5–40-µm long). GCaMP6 sensors thus provide new windows into the organization and dynamics of neural circuits over multiple spatial and temporal scales.
Sensitive protein sensors of calcium have been created; these new tools are shown to report neural activity in cultured neurons, flies and zebrafish and can detect single action potentials and synaptic activation in the mouse visual cortex
in vivo
.
A new sensor for neural activity
Genetically encoded calcium sensors have brought neuronal recording to the tiny brains of invertebrates, but the methodology has lagged behind classical electrophysiology in vertebrates. Now Douglas Kim and colleagues have used selective mutagenesis to engineer a new ultrasensitive probe, GCaMP6, demonstrating improved spatial and temporal resolution
in vivo
, from flies to zebrafish. In addition, in mouse visual cortex GCaMP6 can reliably detect single action potentials and single-spine orientation tuning. GCaMP6 sensors can be used to image large groups of neurons as well as tiny synaptic compartments over multiple imaging sessions separated by months, offering a flexible new tool for brain research and calcium signalling studies.</description><subject>631/1647/1888/2249</subject><subject>Action Potentials</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Calcium - metabolism</subject><subject>Calcium-Binding Proteins - chemistry</subject><subject>Calcium-Binding Proteins - genetics</subject><subject>Cells, Cultured</subject><subject>Danio rerio</subject><subject>Dendritic Spines - metabolism</subject><subject>Eye and associated structures. Visual pathways and centers. Vision</subject><subject>Fluorescent Dyes - chemistry</subject><subject>Fluorescent proteins</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>GABAergic Neurons - metabolism</subject><subject>Humanities and Social Sciences</subject><subject>Insects</subject><subject>Luminescent Proteins - chemistry</subject><subject>Luminescent Proteins - genetics</subject><subject>Mice</subject><subject>Molecular Imaging</subject><subject>multidisciplinary</subject><subject>Mutagenesis</subject><subject>Mutation</subject><subject>Neuroimaging</subject><subject>Neurology</subject><subject>Neurons</subject><subject>Properties</subject><subject>Protein Engineering</subject><subject>Proteins</subject><subject>Pyramidal Cells - metabolism</subject><subject>Pyramidal Cells - physiology</subject><subject>Science</subject><subject>Sensors</subject><subject>Spine</subject><subject>Vertebrates: nervous system and sense organs</subject><subject>Visual Cortex - cytology</subject><subject>Visual Cortex - physiology</subject><issn>0028-0836</issn><issn>1476-4687</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BEC</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp10s1rFDEUAPBBFFurJ-8yWARFp-Y7meOy-FEoCtriMWQzL0PKbGabZMT-92bpandlJIdA8st7L8mrqucYnWFE1ftg8hQBE8rZg-oYMykaJpR8WB0jRFSDFBVH1ZOUrhFCHEv2uDoiVAlFuDquFldDjiZBSD77n1C7YRojJAsh15s4ZvAh1W6MtV-b3oe-DjDFMZihNrYc8Pn2afXImSHBs918Ul19_HC5_NxcfP10vlxcNFZwkRvWGeoEkq1xhBMsO2Ul5U50VGLFFRSFDFphYh3vGEJsJWVLVGtbSx3jLT2pXt_FLWXdTJCyXvtS5zCYAOOUNBblShIzxAs9_Ydej1MsRRfFcMsQYYTdq94MoH1wY3kJuw2qF5RKKpFQ27TNjOohQDTDGMD5snzgX854u_E3eh-dzaAyOlh7Oxv1zcGBYjL8yr2ZUtLn378d2rf_t4vLH8svs9rGMaUITm9i-et4qzHS2_7Se_1V9Ivdy06rNXR_7Z-GKuDVDphkzeCiCdaneycFagWjxb27c6lshR7i3hfN5P0NTBHiJA</recordid><startdate>20130718</startdate><enddate>20130718</enddate><creator>Chen, Tsai-Wen</creator><creator>Wardill, Trevor J.</creator><creator>Sun, Yi</creator><creator>Pulver, Stefan R.</creator><creator>Renninger, Sabine L.</creator><creator>Baohan, Amy</creator><creator>Schreiter, Eric R.</creator><creator>Kerr, Rex A.</creator><creator>Orger, Michael B.</creator><creator>Jayaraman, Vivek</creator><creator>Looger, Loren L.</creator><creator>Svoboda, Karel</creator><creator>Kim, Douglas S.</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>IQODW</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>ATWCN</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7RV</scope><scope>7SN</scope><scope>7SS</scope><scope>7ST</scope><scope>7T5</scope><scope>7TG</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88G</scope><scope>88I</scope><scope>8AF</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>8G5</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>BKSAR</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>GUQSH</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>M2M</scope><scope>M2O</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PCBAR</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PSYQQ</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>Q9U</scope><scope>R05</scope><scope>RC3</scope><scope>S0X</scope><scope>SOI</scope><scope>F1W</scope><scope>H95</scope><scope>L.G</scope></search><sort><creationdate>20130718</creationdate><title>Ultrasensitive fluorescent proteins for imaging neuronal activity</title><author>Chen, Tsai-Wen ; Wardill, Trevor J. ; Sun, Yi ; Pulver, Stefan R. ; Renninger, Sabine L. ; Baohan, Amy ; Schreiter, Eric R. ; Kerr, Rex A. ; Orger, Michael B. ; Jayaraman, Vivek ; Looger, Loren L. ; Svoboda, Karel ; Kim, Douglas S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c656t-4da3f6079af25217d8c735f6d371858ec650a0b12cf5d4004b779289c9c3f4593</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>631/1647/1888/2249</topic><topic>Action Potentials</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Calcium - metabolism</topic><topic>Calcium-Binding Proteins - chemistry</topic><topic>Calcium-Binding Proteins - genetics</topic><topic>Cells, Cultured</topic><topic>Danio rerio</topic><topic>Dendritic Spines - metabolism</topic><topic>Eye and associated structures. Visual pathways and centers. Vision</topic><topic>Fluorescent Dyes - chemistry</topic><topic>Fluorescent proteins</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>GABAergic Neurons - metabolism</topic><topic>Humanities and Social Sciences</topic><topic>Insects</topic><topic>Luminescent Proteins - chemistry</topic><topic>Luminescent Proteins - genetics</topic><topic>Mice</topic><topic>Molecular Imaging</topic><topic>multidisciplinary</topic><topic>Mutagenesis</topic><topic>Mutation</topic><topic>Neuroimaging</topic><topic>Neurology</topic><topic>Neurons</topic><topic>Properties</topic><topic>Protein Engineering</topic><topic>Proteins</topic><topic>Pyramidal Cells - metabolism</topic><topic>Pyramidal Cells - physiology</topic><topic>Science</topic><topic>Sensors</topic><topic>Spine</topic><topic>Vertebrates: nervous system and sense organs</topic><topic>Visual Cortex - cytology</topic><topic>Visual Cortex - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Tsai-Wen</creatorcontrib><creatorcontrib>Wardill, Trevor J.</creatorcontrib><creatorcontrib>Sun, Yi</creatorcontrib><creatorcontrib>Pulver, Stefan R.</creatorcontrib><creatorcontrib>Renninger, Sabine L.</creatorcontrib><creatorcontrib>Baohan, Amy</creatorcontrib><creatorcontrib>Schreiter, Eric R.</creatorcontrib><creatorcontrib>Kerr, Rex A.</creatorcontrib><creatorcontrib>Orger, Michael B.</creatorcontrib><creatorcontrib>Jayaraman, Vivek</creatorcontrib><creatorcontrib>Looger, Loren L.</creatorcontrib><creatorcontrib>Svoboda, Karel</creatorcontrib><creatorcontrib>Kim, Douglas S.</creatorcontrib><collection>Pascal-Francis</collection><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: Middle School</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Environment Abstracts</collection><collection>Immunology Abstracts</collection><collection>Meteorological & Geoastrophysical Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors 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>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</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>Research Library (Alumni Edition)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</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>eLibrary</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Earth, Atmospheric & Aquatic 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>Research Library Prep</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 - Academic</collection><collection>ProQuest Engineering Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Psychology</collection><collection>Research Library</collection><collection>Science Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Engineering Database</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>Earth, Atmospheric & Aquatic Science Database</collection><collection>Materials Science Collection</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 One Psychology</collection><collection>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>ProQuest Central Basic</collection><collection>University of Michigan</collection><collection>Genetics Abstracts</collection><collection>SIRS Editorial</collection><collection>Environment Abstracts</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><jtitle>Nature (London)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Tsai-Wen</au><au>Wardill, Trevor J.</au><au>Sun, Yi</au><au>Pulver, Stefan R.</au><au>Renninger, Sabine L.</au><au>Baohan, Amy</au><au>Schreiter, Eric R.</au><au>Kerr, Rex A.</au><au>Orger, Michael B.</au><au>Jayaraman, Vivek</au><au>Looger, Loren L.</au><au>Svoboda, Karel</au><au>Kim, Douglas S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ultrasensitive fluorescent proteins for imaging neuronal activity</atitle><jtitle>Nature (London)</jtitle><stitle>Nature</stitle><addtitle>Nature</addtitle><date>2013-07-18</date><risdate>2013</risdate><volume>499</volume><issue>7458</issue><spage>295</spage><epage>300</epage><pages>295-300</pages><issn>0028-0836</issn><eissn>1476-4687</eissn><coden>NATUAS</coden><abstract>Fluorescent calcium sensors are widely used to image neural activity. Using structure-based mutagenesis and neuron-based screening, we developed a family of ultrasensitive protein calcium sensors (GCaMP6) that outperformed other sensors in cultured neurons and in zebrafish, flies and mice
in vivo
. In layer 2/3 pyramidal neurons of the mouse visual cortex, GCaMP6 reliably detected single action potentials in neuronal somata and orientation-tuned synaptic calcium transients in individual dendritic spines. The orientation tuning of structurally persistent spines was largely stable over timescales of weeks. Orientation tuning averaged across spine populations predicted the tuning of their parent cell. Although the somata of GABAergic neurons showed little orientation tuning, their dendrites included highly tuned dendritic segments (5–40-µm long). GCaMP6 sensors thus provide new windows into the organization and dynamics of neural circuits over multiple spatial and temporal scales.
Sensitive protein sensors of calcium have been created; these new tools are shown to report neural activity in cultured neurons, flies and zebrafish and can detect single action potentials and synaptic activation in the mouse visual cortex
in vivo
.
A new sensor for neural activity
Genetically encoded calcium sensors have brought neuronal recording to the tiny brains of invertebrates, but the methodology has lagged behind classical electrophysiology in vertebrates. Now Douglas Kim and colleagues have used selective mutagenesis to engineer a new ultrasensitive probe, GCaMP6, demonstrating improved spatial and temporal resolution
in vivo
, from flies to zebrafish. In addition, in mouse visual cortex GCaMP6 can reliably detect single action potentials and single-spine orientation tuning. GCaMP6 sensors can be used to image large groups of neurons as well as tiny synaptic compartments over multiple imaging sessions separated by months, offering a flexible new tool for brain research and calcium signalling studies.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>23868258</pmid><doi>10.1038/nature12354</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0028-0836 |
ispartof | Nature (London), 2013-07, Vol.499 (7458), p.295-300 |
issn | 0028-0836 1476-4687 |
language | eng |
recordid | cdi_proquest_miscellaneous_1668271405 |
source | MEDLINE; SpringerLink Journals; Nature Journals Online |
subjects | 631/1647/1888/2249 Action Potentials Animals Biological and medical sciences Calcium - metabolism Calcium-Binding Proteins - chemistry Calcium-Binding Proteins - genetics Cells, Cultured Danio rerio Dendritic Spines - metabolism Eye and associated structures. Visual pathways and centers. Vision Fluorescent Dyes - chemistry Fluorescent proteins Fundamental and applied biological sciences. Psychology GABAergic Neurons - metabolism Humanities and Social Sciences Insects Luminescent Proteins - chemistry Luminescent Proteins - genetics Mice Molecular Imaging multidisciplinary Mutagenesis Mutation Neuroimaging Neurology Neurons Properties Protein Engineering Proteins Pyramidal Cells - metabolism Pyramidal Cells - physiology Science Sensors Spine Vertebrates: nervous system and sense organs Visual Cortex - cytology Visual Cortex - physiology |
title | Ultrasensitive fluorescent proteins for imaging neuronal activity |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-05T02%3A59%3A15IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Ultrasensitive%20fluorescent%20proteins%20for%20imaging%20neuronal%20activity&rft.jtitle=Nature%20(London)&rft.au=Chen,%20Tsai-Wen&rft.date=2013-07-18&rft.volume=499&rft.issue=7458&rft.spage=295&rft.epage=300&rft.pages=295-300&rft.issn=0028-0836&rft.eissn=1476-4687&rft.coden=NATUAS&rft_id=info:doi/10.1038/nature12354&rft_dat=%3Cgale_proqu%3EA337370689%3C/gale_proqu%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1419402424&rft_id=info:pmid/23868258&rft_galeid=A337370689&rfr_iscdi=true |