A two-photon fluorescence probe for cell membrane imaging under temporal-focusing multiphoton excitation microscopy (TFMPEM)
A small-sized chromophore, BTTA-2OH , manifesting favorable solubility, large two-photon excitation efficiency, and good fluorescence photostability was synthesized to label the membrane of living cells for visualizing the dynamic movement of membrane-related vesicles via a two-photon fluorescence i...
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| Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2021-12, Vol.57 (97), p.13118-13121 |
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| container_issue | 97 |
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| container_title | Chemical communications (Cambridge, England) |
| container_volume | 57 |
| creator | Lee, Wei-Hsuan Lai, Jian-Zong Hsu, Yu-Hsuan Cheng, Fung-Yu Luo, Ching-Lung Huang, Yung-Chin Lin, Tzu-Chau Chien, Fan-Ching |
| description | A small-sized chromophore,
BTTA-2OH
, manifesting favorable solubility, large two-photon excitation efficiency, and good fluorescence photostability was synthesized to label the membrane of living cells for visualizing the dynamic movement of membrane-related vesicles
via
a two-photon fluorescence imaging technique based on wavelength-tunable temporal-focusing multiphoton excitation microscopy.
A small-sized chromophore with comparable photostability and superior two-photon excitation/fluorescence efficiencies was designed and demonstrated to reveal cell membrane-related vesicles
via
temporal-focusing multiphoton excitation microscopy. |
| doi_str_mv | 10.1039/d1cc04962c |
| format | Article |
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BTTA-2OH
, manifesting favorable solubility, large two-photon excitation efficiency, and good fluorescence photostability was synthesized to label the membrane of living cells for visualizing the dynamic movement of membrane-related vesicles
via
a two-photon fluorescence imaging technique based on wavelength-tunable temporal-focusing multiphoton excitation microscopy.
A small-sized chromophore with comparable photostability and superior two-photon excitation/fluorescence efficiencies was designed and demonstrated to reveal cell membrane-related vesicles
via
temporal-focusing multiphoton excitation microscopy.</description><identifier>ISSN: 1359-7345</identifier><identifier>EISSN: 1364-548X</identifier><identifier>DOI: 10.1039/d1cc04962c</identifier><identifier>PMID: 34807218</identifier><language>eng</language><publisher>England: Royal Society of Chemistry</publisher><subject>Cell Membrane - chemistry ; Cell membranes ; Chromophores ; Excitation ; Fluorescent Dyes - chemistry ; Fluorescent indicators ; Humans ; Imaging techniques ; Microscopy ; Microscopy, Fluorescence, Multiphoton ; Optical Imaging ; Photons</subject><ispartof>Chemical communications (Cambridge, England), 2021-12, Vol.57 (97), p.13118-13121</ispartof><rights>Copyright Royal Society of Chemistry 2021</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c337t-205288bedb1cba533865bd3cd389f3ac44b197dc34c62f3d0815be7cfad822e33</citedby><cites>FETCH-LOGICAL-c337t-205288bedb1cba533865bd3cd389f3ac44b197dc34c62f3d0815be7cfad822e33</cites><orcidid>0000-0001-8620-3527 ; 0000-0002-2138-9137</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34807218$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lee, Wei-Hsuan</creatorcontrib><creatorcontrib>Lai, Jian-Zong</creatorcontrib><creatorcontrib>Hsu, Yu-Hsuan</creatorcontrib><creatorcontrib>Cheng, Fung-Yu</creatorcontrib><creatorcontrib>Luo, Ching-Lung</creatorcontrib><creatorcontrib>Huang, Yung-Chin</creatorcontrib><creatorcontrib>Lin, Tzu-Chau</creatorcontrib><creatorcontrib>Chien, Fan-Ching</creatorcontrib><title>A two-photon fluorescence probe for cell membrane imaging under temporal-focusing multiphoton excitation microscopy (TFMPEM)</title><title>Chemical communications (Cambridge, England)</title><addtitle>Chem Commun (Camb)</addtitle><description>A small-sized chromophore,
BTTA-2OH
, manifesting favorable solubility, large two-photon excitation efficiency, and good fluorescence photostability was synthesized to label the membrane of living cells for visualizing the dynamic movement of membrane-related vesicles
via
a two-photon fluorescence imaging technique based on wavelength-tunable temporal-focusing multiphoton excitation microscopy.
A small-sized chromophore with comparable photostability and superior two-photon excitation/fluorescence efficiencies was designed and demonstrated to reveal cell membrane-related vesicles
via
temporal-focusing multiphoton excitation microscopy.</description><subject>Cell Membrane - chemistry</subject><subject>Cell membranes</subject><subject>Chromophores</subject><subject>Excitation</subject><subject>Fluorescent Dyes - chemistry</subject><subject>Fluorescent indicators</subject><subject>Humans</subject><subject>Imaging techniques</subject><subject>Microscopy</subject><subject>Microscopy, Fluorescence, Multiphoton</subject><subject>Optical Imaging</subject><subject>Photons</subject><issn>1359-7345</issn><issn>1364-548X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkd9r1zAUxYMo7oe--K4EfJlCNclN2_Rx1E2FDX2Y4Ftpbm5nR9t0SYsO_OOX-v06wbzkcPPhcE8OYy-keCcFVO-dRBS6KhQ-YocSCp3l2nx_vOm8ykrQ-QE7ivFGpCNz85QdgDaiVNIcst-nfPnps_mHX_zEu2H1gSLShMTn4C3xzgeONAx8pNGGdiLej-11P13zdXIU-ELj7EM7ZJ3HNW7zcR2Wfm9Iv7Bf2qVPcuwx-Ih-vuMnV-eXX88u3zxjT7p2iPR8fx-zb-dnV_Wn7OLLx8_16UWGAOWSKZErYyw5K9G2OYApcusAHZiqgxa1trIqHYLGQnXghJG5pRK71hmlCOCYnex8U6TbleLSjH3cQqU4fo2NKoQwSstSJPT1f-iNX8OUttuoUkNV6iJRb3fUFikG6po5pG8Jd40UzdZJ80HW9Z9O6gS_2luudiT3gP4tIQEvd0CI-PD6r1S4B2XTkkU</recordid><startdate>20211207</startdate><enddate>20211207</enddate><creator>Lee, Wei-Hsuan</creator><creator>Lai, Jian-Zong</creator><creator>Hsu, Yu-Hsuan</creator><creator>Cheng, Fung-Yu</creator><creator>Luo, Ching-Lung</creator><creator>Huang, Yung-Chin</creator><creator>Lin, Tzu-Chau</creator><creator>Chien, Fan-Ching</creator><general>Royal Society of Chemistry</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>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-8620-3527</orcidid><orcidid>https://orcid.org/0000-0002-2138-9137</orcidid></search><sort><creationdate>20211207</creationdate><title>A two-photon fluorescence probe for cell membrane imaging under temporal-focusing multiphoton excitation microscopy (TFMPEM)</title><author>Lee, Wei-Hsuan ; Lai, Jian-Zong ; Hsu, Yu-Hsuan ; Cheng, Fung-Yu ; Luo, Ching-Lung ; Huang, Yung-Chin ; Lin, Tzu-Chau ; Chien, Fan-Ching</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c337t-205288bedb1cba533865bd3cd389f3ac44b197dc34c62f3d0815be7cfad822e33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Cell Membrane - chemistry</topic><topic>Cell membranes</topic><topic>Chromophores</topic><topic>Excitation</topic><topic>Fluorescent Dyes - chemistry</topic><topic>Fluorescent indicators</topic><topic>Humans</topic><topic>Imaging techniques</topic><topic>Microscopy</topic><topic>Microscopy, Fluorescence, Multiphoton</topic><topic>Optical Imaging</topic><topic>Photons</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, Wei-Hsuan</creatorcontrib><creatorcontrib>Lai, Jian-Zong</creatorcontrib><creatorcontrib>Hsu, Yu-Hsuan</creatorcontrib><creatorcontrib>Cheng, Fung-Yu</creatorcontrib><creatorcontrib>Luo, Ching-Lung</creatorcontrib><creatorcontrib>Huang, Yung-Chin</creatorcontrib><creatorcontrib>Lin, Tzu-Chau</creatorcontrib><creatorcontrib>Chien, Fan-Ching</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Chemical communications (Cambridge, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, Wei-Hsuan</au><au>Lai, Jian-Zong</au><au>Hsu, Yu-Hsuan</au><au>Cheng, Fung-Yu</au><au>Luo, Ching-Lung</au><au>Huang, Yung-Chin</au><au>Lin, Tzu-Chau</au><au>Chien, Fan-Ching</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A two-photon fluorescence probe for cell membrane imaging under temporal-focusing multiphoton excitation microscopy (TFMPEM)</atitle><jtitle>Chemical communications (Cambridge, England)</jtitle><addtitle>Chem Commun (Camb)</addtitle><date>2021-12-07</date><risdate>2021</risdate><volume>57</volume><issue>97</issue><spage>13118</spage><epage>13121</epage><pages>13118-13121</pages><issn>1359-7345</issn><eissn>1364-548X</eissn><abstract>A small-sized chromophore,
BTTA-2OH
, manifesting favorable solubility, large two-photon excitation efficiency, and good fluorescence photostability was synthesized to label the membrane of living cells for visualizing the dynamic movement of membrane-related vesicles
via
a two-photon fluorescence imaging technique based on wavelength-tunable temporal-focusing multiphoton excitation microscopy.
A small-sized chromophore with comparable photostability and superior two-photon excitation/fluorescence efficiencies was designed and demonstrated to reveal cell membrane-related vesicles
via
temporal-focusing multiphoton excitation microscopy.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>34807218</pmid><doi>10.1039/d1cc04962c</doi><tpages>4</tpages><orcidid>https://orcid.org/0000-0001-8620-3527</orcidid><orcidid>https://orcid.org/0000-0002-2138-9137</orcidid></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 1359-7345 |
| ispartof | Chemical communications (Cambridge, England), 2021-12, Vol.57 (97), p.13118-13121 |
| issn | 1359-7345 1364-548X |
| language | eng |
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| source | MEDLINE; Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
| subjects | Cell Membrane - chemistry Cell membranes Chromophores Excitation Fluorescent Dyes - chemistry Fluorescent indicators Humans Imaging techniques Microscopy Microscopy, Fluorescence, Multiphoton Optical Imaging Photons |
| title | A two-photon fluorescence probe for cell membrane imaging under temporal-focusing multiphoton excitation microscopy (TFMPEM) |
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