Cyanobacterial stabilized phycobilisomes as fluorochromes for extracellular antigen detection by flow cytometry
Phycobilisomes are cyanobacterial photosynthetic energy transfer complexes partly composed of phycobiliproteins, proteins that are widely used as conjugable fluorochromes for flow cytometry. The brightness and photostability of phycobiliproteins suggest that intact phycobilisomes could constitute ev...
Gespeichert in:
Veröffentlicht in: | Journal of immunological methods 2001-08, Vol.254 (1), p.13-30 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 30 |
---|---|
container_issue | 1 |
container_start_page | 13 |
container_title | Journal of immunological methods |
container_volume | 254 |
creator | Telford, William G Moss, Mark W Morseman, John P Allnutt, F.C.Thomas |
description | Phycobilisomes are cyanobacterial photosynthetic energy transfer complexes partly composed of phycobiliproteins, proteins that are widely used as conjugable fluorochromes for flow cytometry. The brightness and photostability of phycobiliproteins suggest that intact phycobilisomes could constitute even brighter probes for fluorescence-based detection systems. Stabilized phycobilisomes have been isolated and the red-excited, far red-emitting
Spirulina platensis-derived complex PBXL-3 was accessed as a fluorochrome for flow cytometric immunodetection of surface antigens on immune cells. Although the large size of intact phycobilisomes initially precluded efficient cell surface labeling, the addition of a PEG spacer arm between PBXL-3 and its conjugated avidin molecule (designated PBXL-3L) reduced the steric hindrance associated with the high molecular weight PBXL complex. PBXL-3L increased the surface labeling surface-to-noise ratio and subsequent sensitivity by several-fold over commonly used red-excited fluorochromes such as APC. Interestingly, low power laser sources (including helium–neon and red diode) were particularly efficient at exciting PBXL-3. PBXL-3 was also compatible in with other fluorochromes for multicolor flow cytometry applications. In summary, PBXL-3 was found to possess superior sensitivity and efficiency for flow cytometric immunodetection, particularly with low power laser sources. |
doi_str_mv | 10.1016/S0022-1759(01)00367-2 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_70924929</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0022175901003672</els_id><sourcerecordid>70924929</sourcerecordid><originalsourceid>FETCH-LOGICAL-c474t-f2cede40e20b726923b7104cba7ad19eb746c3fca46b3f1ffccc8252e2d99cb13</originalsourceid><addsrcrecordid>eNqFkc2O1DAQhC0EYoeFRwD5AoJDoO048eS0QiP-pJU4AGfL7rRZo0w82A4Qnp5kZsQe92S19VV3qYqxpwJeCxDtmy8AUlZCN91LEK8A6lZX8h7biK2Wle6guc82_5EL9ijnHwAgoIWH7EIIBa1oYMPibrZjdBYLpWAHnot1YQh_qeeHmxnjOuS4p8xt5n6YYop4k44fPiZOf0qySMMwDTZxO5bwnUbeUyEsIY7czYso_uY4l0VT0vyYPfB2yPTk_F6yb-_ffd19rK4_f_i0e3tdodKqVF4i9aSAJDgt207WTgtQ6Ky2vejIadVi7dGq1tVeeI-IW9lIkn3XoRP1JXtx2ntI8edEuZh9yKtRO1KcstHQSdXJ7k5QbGG7xLaCzQnEFHNO5M0hhb1NsxFg1krMsRKz5m1AmGMlRi66Z-cDk9tTf6s6d7AAz8-AzWgHn-yIId9ySrRSNauBqxNHS26_AiWTMdC4BBXSErfpY7jDyj-1-Kuo</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>18080109</pqid></control><display><type>article</type><title>Cyanobacterial stabilized phycobilisomes as fluorochromes for extracellular antigen detection by flow cytometry</title><source>MEDLINE</source><source>Access via ScienceDirect (Elsevier)</source><creator>Telford, William G ; Moss, Mark W ; Morseman, John P ; Allnutt, F.C.Thomas</creator><creatorcontrib>Telford, William G ; Moss, Mark W ; Morseman, John P ; Allnutt, F.C.Thomas</creatorcontrib><description>Phycobilisomes are cyanobacterial photosynthetic energy transfer complexes partly composed of phycobiliproteins, proteins that are widely used as conjugable fluorochromes for flow cytometry. The brightness and photostability of phycobiliproteins suggest that intact phycobilisomes could constitute even brighter probes for fluorescence-based detection systems. Stabilized phycobilisomes have been isolated and the red-excited, far red-emitting
Spirulina platensis-derived complex PBXL-3 was accessed as a fluorochrome for flow cytometric immunodetection of surface antigens on immune cells. Although the large size of intact phycobilisomes initially precluded efficient cell surface labeling, the addition of a PEG spacer arm between PBXL-3 and its conjugated avidin molecule (designated PBXL-3L) reduced the steric hindrance associated with the high molecular weight PBXL complex. PBXL-3L increased the surface labeling surface-to-noise ratio and subsequent sensitivity by several-fold over commonly used red-excited fluorochromes such as APC. Interestingly, low power laser sources (including helium–neon and red diode) were particularly efficient at exciting PBXL-3. PBXL-3 was also compatible in with other fluorochromes for multicolor flow cytometry applications. In summary, PBXL-3 was found to possess superior sensitivity and efficiency for flow cytometric immunodetection, particularly with low power laser sources.</description><identifier>ISSN: 0022-1759</identifier><identifier>EISSN: 1872-7905</identifier><identifier>DOI: 10.1016/S0022-1759(01)00367-2</identifier><identifier>PMID: 11406150</identifier><identifier>CODEN: JIMMBG</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Animals ; Antigens, Surface - analysis ; Bacterial Proteins ; Biological and medical sciences ; Cell Line ; Cells, Cultured ; Cyanobacteria ; Diverse techniques ; Flow cytometry ; Flow Cytometry - methods ; Fluorescent Dyes ; fluorochromes ; Fundamental and applied biological sciences. Psychology ; Fundamental immunology ; Humans ; Light-Harvesting Protein Complexes ; Mice ; Microbiology ; Molecular and cellular biology ; Molecular immunology ; Phycobiliprotein ; phycobiliproteins ; Phycobilisome ; Phycobilisomes ; Plant Proteins ; Spirulina platensis ; Techniques</subject><ispartof>Journal of immunological methods, 2001-08, Vol.254 (1), p.13-30</ispartof><rights>2001 Elsevier Science B.V.</rights><rights>2002 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-f2cede40e20b726923b7104cba7ad19eb746c3fca46b3f1ffccc8252e2d99cb13</citedby><cites>FETCH-LOGICAL-c474t-f2cede40e20b726923b7104cba7ad19eb746c3fca46b3f1ffccc8252e2d99cb13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0022-1759(01)00367-2$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14162459$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11406150$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Telford, William G</creatorcontrib><creatorcontrib>Moss, Mark W</creatorcontrib><creatorcontrib>Morseman, John P</creatorcontrib><creatorcontrib>Allnutt, F.C.Thomas</creatorcontrib><title>Cyanobacterial stabilized phycobilisomes as fluorochromes for extracellular antigen detection by flow cytometry</title><title>Journal of immunological methods</title><addtitle>J Immunol Methods</addtitle><description>Phycobilisomes are cyanobacterial photosynthetic energy transfer complexes partly composed of phycobiliproteins, proteins that are widely used as conjugable fluorochromes for flow cytometry. The brightness and photostability of phycobiliproteins suggest that intact phycobilisomes could constitute even brighter probes for fluorescence-based detection systems. Stabilized phycobilisomes have been isolated and the red-excited, far red-emitting
Spirulina platensis-derived complex PBXL-3 was accessed as a fluorochrome for flow cytometric immunodetection of surface antigens on immune cells. Although the large size of intact phycobilisomes initially precluded efficient cell surface labeling, the addition of a PEG spacer arm between PBXL-3 and its conjugated avidin molecule (designated PBXL-3L) reduced the steric hindrance associated with the high molecular weight PBXL complex. PBXL-3L increased the surface labeling surface-to-noise ratio and subsequent sensitivity by several-fold over commonly used red-excited fluorochromes such as APC. Interestingly, low power laser sources (including helium–neon and red diode) were particularly efficient at exciting PBXL-3. PBXL-3 was also compatible in with other fluorochromes for multicolor flow cytometry applications. In summary, PBXL-3 was found to possess superior sensitivity and efficiency for flow cytometric immunodetection, particularly with low power laser sources.</description><subject>Animals</subject><subject>Antigens, Surface - analysis</subject><subject>Bacterial Proteins</subject><subject>Biological and medical sciences</subject><subject>Cell Line</subject><subject>Cells, Cultured</subject><subject>Cyanobacteria</subject><subject>Diverse techniques</subject><subject>Flow cytometry</subject><subject>Flow Cytometry - methods</subject><subject>Fluorescent Dyes</subject><subject>fluorochromes</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Fundamental immunology</subject><subject>Humans</subject><subject>Light-Harvesting Protein Complexes</subject><subject>Mice</subject><subject>Microbiology</subject><subject>Molecular and cellular biology</subject><subject>Molecular immunology</subject><subject>Phycobiliprotein</subject><subject>phycobiliproteins</subject><subject>Phycobilisome</subject><subject>Phycobilisomes</subject><subject>Plant Proteins</subject><subject>Spirulina platensis</subject><subject>Techniques</subject><issn>0022-1759</issn><issn>1872-7905</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc2O1DAQhC0EYoeFRwD5AoJDoO048eS0QiP-pJU4AGfL7rRZo0w82A4Qnp5kZsQe92S19VV3qYqxpwJeCxDtmy8AUlZCN91LEK8A6lZX8h7biK2Wle6guc82_5EL9ijnHwAgoIWH7EIIBa1oYMPibrZjdBYLpWAHnot1YQh_qeeHmxnjOuS4p8xt5n6YYop4k44fPiZOf0qySMMwDTZxO5bwnUbeUyEsIY7czYso_uY4l0VT0vyYPfB2yPTk_F6yb-_ffd19rK4_f_i0e3tdodKqVF4i9aSAJDgt207WTgtQ6Ky2vejIadVi7dGq1tVeeI-IW9lIkn3XoRP1JXtx2ntI8edEuZh9yKtRO1KcstHQSdXJ7k5QbGG7xLaCzQnEFHNO5M0hhb1NsxFg1krMsRKz5m1AmGMlRi66Z-cDk9tTf6s6d7AAz8-AzWgHn-yIId9ySrRSNauBqxNHS26_AiWTMdC4BBXSErfpY7jDyj-1-Kuo</recordid><startdate>20010801</startdate><enddate>20010801</enddate><creator>Telford, William G</creator><creator>Moss, Mark W</creator><creator>Morseman, John P</creator><creator>Allnutt, F.C.Thomas</creator><general>Elsevier B.V</general><general>Elsevier</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>7T5</scope><scope>8FD</scope><scope>F1W</scope><scope>FR3</scope><scope>H94</scope><scope>H95</scope><scope>H99</scope><scope>L.F</scope><scope>L.G</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20010801</creationdate><title>Cyanobacterial stabilized phycobilisomes as fluorochromes for extracellular antigen detection by flow cytometry</title><author>Telford, William G ; Moss, Mark W ; Morseman, John P ; Allnutt, F.C.Thomas</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-f2cede40e20b726923b7104cba7ad19eb746c3fca46b3f1ffccc8252e2d99cb13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Animals</topic><topic>Antigens, Surface - analysis</topic><topic>Bacterial Proteins</topic><topic>Biological and medical sciences</topic><topic>Cell Line</topic><topic>Cells, Cultured</topic><topic>Cyanobacteria</topic><topic>Diverse techniques</topic><topic>Flow cytometry</topic><topic>Flow Cytometry - methods</topic><topic>Fluorescent Dyes</topic><topic>fluorochromes</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Fundamental immunology</topic><topic>Humans</topic><topic>Light-Harvesting Protein Complexes</topic><topic>Mice</topic><topic>Microbiology</topic><topic>Molecular and cellular biology</topic><topic>Molecular immunology</topic><topic>Phycobiliprotein</topic><topic>phycobiliproteins</topic><topic>Phycobilisome</topic><topic>Phycobilisomes</topic><topic>Plant Proteins</topic><topic>Spirulina platensis</topic><topic>Techniques</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Telford, William G</creatorcontrib><creatorcontrib>Moss, Mark W</creatorcontrib><creatorcontrib>Morseman, John P</creatorcontrib><creatorcontrib>Allnutt, F.C.Thomas</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>Immunology Abstracts</collection><collection>Technology Research Database</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 1: Biological Sciences & Living Resources</collection><collection>ASFA: Marine Biotechnology Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Marine Biotechnology Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of immunological methods</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Telford, William G</au><au>Moss, Mark W</au><au>Morseman, John P</au><au>Allnutt, F.C.Thomas</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cyanobacterial stabilized phycobilisomes as fluorochromes for extracellular antigen detection by flow cytometry</atitle><jtitle>Journal of immunological methods</jtitle><addtitle>J Immunol Methods</addtitle><date>2001-08-01</date><risdate>2001</risdate><volume>254</volume><issue>1</issue><spage>13</spage><epage>30</epage><pages>13-30</pages><issn>0022-1759</issn><eissn>1872-7905</eissn><coden>JIMMBG</coden><abstract>Phycobilisomes are cyanobacterial photosynthetic energy transfer complexes partly composed of phycobiliproteins, proteins that are widely used as conjugable fluorochromes for flow cytometry. The brightness and photostability of phycobiliproteins suggest that intact phycobilisomes could constitute even brighter probes for fluorescence-based detection systems. Stabilized phycobilisomes have been isolated and the red-excited, far red-emitting
Spirulina platensis-derived complex PBXL-3 was accessed as a fluorochrome for flow cytometric immunodetection of surface antigens on immune cells. Although the large size of intact phycobilisomes initially precluded efficient cell surface labeling, the addition of a PEG spacer arm between PBXL-3 and its conjugated avidin molecule (designated PBXL-3L) reduced the steric hindrance associated with the high molecular weight PBXL complex. PBXL-3L increased the surface labeling surface-to-noise ratio and subsequent sensitivity by several-fold over commonly used red-excited fluorochromes such as APC. Interestingly, low power laser sources (including helium–neon and red diode) were particularly efficient at exciting PBXL-3. PBXL-3 was also compatible in with other fluorochromes for multicolor flow cytometry applications. In summary, PBXL-3 was found to possess superior sensitivity and efficiency for flow cytometric immunodetection, particularly with low power laser sources.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>11406150</pmid><doi>10.1016/S0022-1759(01)00367-2</doi><tpages>18</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0022-1759 |
ispartof | Journal of immunological methods, 2001-08, Vol.254 (1), p.13-30 |
issn | 0022-1759 1872-7905 |
language | eng |
recordid | cdi_proquest_miscellaneous_70924929 |
source | MEDLINE; Access via ScienceDirect (Elsevier) |
subjects | Animals Antigens, Surface - analysis Bacterial Proteins Biological and medical sciences Cell Line Cells, Cultured Cyanobacteria Diverse techniques Flow cytometry Flow Cytometry - methods Fluorescent Dyes fluorochromes Fundamental and applied biological sciences. Psychology Fundamental immunology Humans Light-Harvesting Protein Complexes Mice Microbiology Molecular and cellular biology Molecular immunology Phycobiliprotein phycobiliproteins Phycobilisome Phycobilisomes Plant Proteins Spirulina platensis Techniques |
title | Cyanobacterial stabilized phycobilisomes as fluorochromes for extracellular antigen detection by flow cytometry |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-03T23%3A21%3A33IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Cyanobacterial%20stabilized%20phycobilisomes%20as%20fluorochromes%20for%20extracellular%20antigen%20detection%20by%20flow%20cytometry&rft.jtitle=Journal%20of%20immunological%20methods&rft.au=Telford,%20William%20G&rft.date=2001-08-01&rft.volume=254&rft.issue=1&rft.spage=13&rft.epage=30&rft.pages=13-30&rft.issn=0022-1759&rft.eissn=1872-7905&rft.coden=JIMMBG&rft_id=info:doi/10.1016/S0022-1759(01)00367-2&rft_dat=%3Cproquest_cross%3E70924929%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=18080109&rft_id=info:pmid/11406150&rft_els_id=S0022175901003672&rfr_iscdi=true |