Single Molecule Spectroscopy on the Light-Harvesting Complex II of Higher Plants
Spectroscopic and polarization properties of single light-harvesting complexes of higher plants (LHC-II) were studied at both room temperature and T < 5 K. Monomeric complexes emit roughly linearly polarized fluorescence light thus indicating the existence of only one emitting state. Most probabl...
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Veröffentlicht in: | Biophysical journal 2001-07, Vol.81 (1), p.556-562 |
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creator | Tietz, Carsten Jelezko, Fedor Gerken, Uwe Schuler, Sebastian Schubert, Axel Rogl, Hans Wrachtrup, Jörg |
description | Spectroscopic and polarization properties of single light-harvesting complexes of higher plants (LHC-II) were studied at both room temperature and T
<
5
K. Monomeric complexes emit roughly linearly polarized fluorescence light thus indicating the existence of only one emitting state. Most probably this observation is explained by efficient triplet quenching restricted to one chlorophyll
a (Chl
a) molecule or by rather irreversible energy transfer within the pool of Chl
a molecules. LHC-II complexes in the trimeric (native) arrangement bleach in a number of steps, suggesting localization of excitations within the monomeric subunits. Interpretation of the fluorescence polarization properties of trimers requires the assumption of transition dipole moments tilted out of the symmetry plane of the complex. Low-temperature fluorescence emission of trimers is characterized by several narrow spectral lines. Even at lowest excitation intensities, we observed considerable spectral diffusion most probably due to low temperature protein dynamics. These results also indicate weak interaction between Chls belonging to different monomeric subunits within the trimer thus leading to a localization of excitations within the monomer. The experimental results demonstrate the feasibility of polarization sensitive studies on single LHC-II complexes and suggest an application for determination of the Chl transition-dipole moment orientations, a key issue in understanding the structure-function relationships. |
doi_str_mv | 10.1016/S0006-3495(01)75722-0 |
format | Article |
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<
5
K. Monomeric complexes emit roughly linearly polarized fluorescence light thus indicating the existence of only one emitting state. Most probably this observation is explained by efficient triplet quenching restricted to one chlorophyll
a (Chl
a) molecule or by rather irreversible energy transfer within the pool of Chl
a molecules. LHC-II complexes in the trimeric (native) arrangement bleach in a number of steps, suggesting localization of excitations within the monomeric subunits. Interpretation of the fluorescence polarization properties of trimers requires the assumption of transition dipole moments tilted out of the symmetry plane of the complex. Low-temperature fluorescence emission of trimers is characterized by several narrow spectral lines. Even at lowest excitation intensities, we observed considerable spectral diffusion most probably due to low temperature protein dynamics. These results also indicate weak interaction between Chls belonging to different monomeric subunits within the trimer thus leading to a localization of excitations within the monomer. The experimental results demonstrate the feasibility of polarization sensitive studies on single LHC-II complexes and suggest an application for determination of the Chl transition-dipole moment orientations, a key issue in understanding the structure-function relationships.</description><identifier>ISSN: 0006-3495</identifier><identifier>EISSN: 1542-0086</identifier><identifier>DOI: 10.1016/S0006-3495(01)75722-0</identifier><identifier>PMID: 11423437</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Biology ; Flowers & plants ; Fluorescence Polarization ; Light-Harvesting Protein Complexes ; Molecular Conformation ; Molecules ; Photosynthetic Reaction Center Complex Proteins - chemistry ; Photosynthetic Reaction Center Complex Proteins - metabolism ; Physics ; Pisum sativum ; Spectrometry, Fluorescence - methods ; Spectrum analysis ; Temperature</subject><ispartof>Biophysical journal, 2001-07, Vol.81 (1), p.556-562</ispartof><rights>2001 The Biophysical Society</rights><rights>Copyright Biophysical Society Jul 2001</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c490t-9dd75657e861ce14275b1b6448e68cc35259445bf90fb5a897b9db7b2476cf0f3</citedby><cites>FETCH-LOGICAL-c490t-9dd75657e861ce14275b1b6448e68cc35259445bf90fb5a897b9db7b2476cf0f3</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/PMC1301534/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0006-3495(01)75722-0$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,3548,27922,27923,45993,53789,53791</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11423437$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tietz, Carsten</creatorcontrib><creatorcontrib>Jelezko, Fedor</creatorcontrib><creatorcontrib>Gerken, Uwe</creatorcontrib><creatorcontrib>Schuler, Sebastian</creatorcontrib><creatorcontrib>Schubert, Axel</creatorcontrib><creatorcontrib>Rogl, Hans</creatorcontrib><creatorcontrib>Wrachtrup, Jörg</creatorcontrib><title>Single Molecule Spectroscopy on the Light-Harvesting Complex II of Higher Plants</title><title>Biophysical journal</title><addtitle>Biophys J</addtitle><description>Spectroscopic and polarization properties of single light-harvesting complexes of higher plants (LHC-II) were studied at both room temperature and T
<
5
K. Monomeric complexes emit roughly linearly polarized fluorescence light thus indicating the existence of only one emitting state. Most probably this observation is explained by efficient triplet quenching restricted to one chlorophyll
a (Chl
a) molecule or by rather irreversible energy transfer within the pool of Chl
a molecules. LHC-II complexes in the trimeric (native) arrangement bleach in a number of steps, suggesting localization of excitations within the monomeric subunits. Interpretation of the fluorescence polarization properties of trimers requires the assumption of transition dipole moments tilted out of the symmetry plane of the complex. Low-temperature fluorescence emission of trimers is characterized by several narrow spectral lines. Even at lowest excitation intensities, we observed considerable spectral diffusion most probably due to low temperature protein dynamics. These results also indicate weak interaction between Chls belonging to different monomeric subunits within the trimer thus leading to a localization of excitations within the monomer. The experimental results demonstrate the feasibility of polarization sensitive studies on single LHC-II complexes and suggest an application for determination of the Chl transition-dipole moment orientations, a key issue in understanding the structure-function relationships.</description><subject>Biology</subject><subject>Flowers & plants</subject><subject>Fluorescence Polarization</subject><subject>Light-Harvesting Protein Complexes</subject><subject>Molecular Conformation</subject><subject>Molecules</subject><subject>Photosynthetic Reaction Center Complex Proteins - chemistry</subject><subject>Photosynthetic Reaction Center Complex Proteins - metabolism</subject><subject>Physics</subject><subject>Pisum sativum</subject><subject>Spectrometry, Fluorescence - methods</subject><subject>Spectrum analysis</subject><subject>Temperature</subject><issn>0006-3495</issn><issn>1542-0086</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqFkU1v00AQhleIiobATwCtOFRwMMza--G9gKoISKQgKgXOK3s9TrZyvO6uHdF_z7aJWuDCaUaaZz7eeQl5xeA9AyY_bABAZgXX4i2wd0qoPM_gCZkxwVMCpXxKZg_IOXke4zUAywWwZ-ScMZ4XvFAzcrVx_bZD-s13aKeUbAa0Y_DR-uGW-p6OO6Rrt92N2bIKB4xj4unC74cOf9HVivqWLlMZA73qqn6ML8hZW3URX57inPz88vnHYpmtv39dLS7XmeUaxkw3jRJSKCwls5jOUaJmteS8RFlaW4hcaM5F3Wpoa1GVWtW6qVWdcyVtC20xJx-Pc4ep3mNjsR9D1ZkhuH0Vbo2vnPm70rud2fqDYQUwkcTPycVpQPA3UxJm9i5a7JIK9FM0CjTXHIoEvvkHvPZT6JM4kzOhmMxLmSBxhGz6XQzYPlzCwNwZZu4NM3duGGDm3jADqe_1nzIeu04OJeDTEcD0zIPDYKJ12FtsXEhOmca7_6z4DWl5pP0</recordid><startdate>20010701</startdate><enddate>20010701</enddate><creator>Tietz, Carsten</creator><creator>Jelezko, Fedor</creator><creator>Gerken, Uwe</creator><creator>Schuler, Sebastian</creator><creator>Schubert, Axel</creator><creator>Rogl, Hans</creator><creator>Wrachtrup, Jörg</creator><general>Elsevier Inc</general><general>Biophysical Society</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>3V.</scope><scope>7QO</scope><scope>7QP</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</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>ABUWG</scope><scope>AEUYN</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>CCPQU</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>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M2P</scope><scope>M7P</scope><scope>MBDVC</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>S0X</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20010701</creationdate><title>Single Molecule Spectroscopy on the Light-Harvesting Complex II of Higher Plants</title><author>Tietz, Carsten ; Jelezko, Fedor ; Gerken, Uwe ; Schuler, Sebastian ; Schubert, Axel ; Rogl, Hans ; Wrachtrup, Jörg</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c490t-9dd75657e861ce14275b1b6448e68cc35259445bf90fb5a897b9db7b2476cf0f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Biology</topic><topic>Flowers & plants</topic><topic>Fluorescence Polarization</topic><topic>Light-Harvesting Protein Complexes</topic><topic>Molecular Conformation</topic><topic>Molecules</topic><topic>Photosynthetic Reaction Center Complex Proteins - chemistry</topic><topic>Photosynthetic Reaction Center Complex Proteins - metabolism</topic><topic>Physics</topic><topic>Pisum sativum</topic><topic>Spectrometry, Fluorescence - methods</topic><topic>Spectrum analysis</topic><topic>Temperature</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tietz, Carsten</creatorcontrib><creatorcontrib>Jelezko, Fedor</creatorcontrib><creatorcontrib>Gerken, Uwe</creatorcontrib><creatorcontrib>Schuler, Sebastian</creatorcontrib><creatorcontrib>Schubert, Axel</creatorcontrib><creatorcontrib>Rogl, Hans</creatorcontrib><creatorcontrib>Wrachtrup, Jörg</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>ProQuest Central (Corporate)</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences 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>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</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>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>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection (ProQuest)</collection><collection>ProQuest One Community College</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>ProQuest Biological Science Collection</collection><collection>Agricultural Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</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>SIRS Editorial</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Biophysical journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tietz, Carsten</au><au>Jelezko, Fedor</au><au>Gerken, Uwe</au><au>Schuler, Sebastian</au><au>Schubert, Axel</au><au>Rogl, Hans</au><au>Wrachtrup, Jörg</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Single Molecule Spectroscopy on the Light-Harvesting Complex II of Higher Plants</atitle><jtitle>Biophysical journal</jtitle><addtitle>Biophys J</addtitle><date>2001-07-01</date><risdate>2001</risdate><volume>81</volume><issue>1</issue><spage>556</spage><epage>562</epage><pages>556-562</pages><issn>0006-3495</issn><eissn>1542-0086</eissn><abstract>Spectroscopic and polarization properties of single light-harvesting complexes of higher plants (LHC-II) were studied at both room temperature and T
<
5
K. Monomeric complexes emit roughly linearly polarized fluorescence light thus indicating the existence of only one emitting state. Most probably this observation is explained by efficient triplet quenching restricted to one chlorophyll
a (Chl
a) molecule or by rather irreversible energy transfer within the pool of Chl
a molecules. LHC-II complexes in the trimeric (native) arrangement bleach in a number of steps, suggesting localization of excitations within the monomeric subunits. Interpretation of the fluorescence polarization properties of trimers requires the assumption of transition dipole moments tilted out of the symmetry plane of the complex. Low-temperature fluorescence emission of trimers is characterized by several narrow spectral lines. Even at lowest excitation intensities, we observed considerable spectral diffusion most probably due to low temperature protein dynamics. These results also indicate weak interaction between Chls belonging to different monomeric subunits within the trimer thus leading to a localization of excitations within the monomer. The experimental results demonstrate the feasibility of polarization sensitive studies on single LHC-II complexes and suggest an application for determination of the Chl transition-dipole moment orientations, a key issue in understanding the structure-function relationships.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>11423437</pmid><doi>10.1016/S0006-3495(01)75722-0</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Biology Flowers & plants Fluorescence Polarization Light-Harvesting Protein Complexes Molecular Conformation Molecules Photosynthetic Reaction Center Complex Proteins - chemistry Photosynthetic Reaction Center Complex Proteins - metabolism Physics Pisum sativum Spectrometry, Fluorescence - methods Spectrum analysis Temperature |
title | Single Molecule Spectroscopy on the Light-Harvesting Complex II of Higher Plants |
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