A fluorescent light-up probe based on AIE and ESIPT processes for β-galactosidase activity detection and visualization in living cells
A novel fluorescent probe SA-βGal is reported here with light-up response to β-galactosidase. SA-βGal possesses the β-galactopyranoside group to react with β-galactosidase and releases the fluorescent salicylaldehyde azine with both aggregation induced emission (AIE) and excited-state intramolecular...
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Veröffentlicht in: | Journal of materials chemistry. B, Materials for biology and medicine Materials for biology and medicine, 2015-01, Vol.3 (47), p.9168-9172 |
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container_title | Journal of materials chemistry. B, Materials for biology and medicine |
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creator | Peng, Lu Gao, Meng Cai, Xiaolei Zhang, Ruoyu Li, Kai Feng, Guangxue Tong, Aijun Liu, Bin |
description | A novel fluorescent probe SA-βGal is reported here with light-up response to β-galactosidase. SA-βGal possesses the β-galactopyranoside group to react with β-galactosidase and releases the fluorescent salicylaldehyde azine with both aggregation induced emission (AIE) and excited-state intramolecular proton transfer (ESIPT) characteristics. The linear fluorescent response enables the in vitro quantification of β-galactosidase activity in a range of 0-0.1 U mL
with a detection limit of 0.014 U mL
. The probe exhibits significant advantages, such as no self-quenching at high concentrations, a large Stokes shift (190 nm) and high specificity to β-galactosidase with an excellent light-up ratio of 820 fold. Moreover, thanks to its good retention in living cells, the application of SA-βGal for the imaging of cellular β-galactosidase was also achieved with high contrast. |
doi_str_mv | 10.1039/c5tb01938a |
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with a detection limit of 0.014 U mL
. The probe exhibits significant advantages, such as no self-quenching at high concentrations, a large Stokes shift (190 nm) and high specificity to β-galactosidase with an excellent light-up ratio of 820 fold. Moreover, thanks to its good retention in living cells, the application of SA-βGal for the imaging of cellular β-galactosidase was also achieved with high contrast.</description><identifier>ISSN: 2050-750X</identifier><identifier>EISSN: 2050-7518</identifier><identifier>DOI: 10.1039/c5tb01938a</identifier><identifier>PMID: 32263131</identifier><language>eng</language><publisher>England</publisher><ispartof>Journal of materials chemistry. B, Materials for biology and medicine, 2015-01, Vol.3 (47), p.9168-9172</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c328t-cd7dfb9358133b3409dc71c34e697d96d5f76ab14e0caf130769adf78955fcaf3</citedby><cites>FETCH-LOGICAL-c328t-cd7dfb9358133b3409dc71c34e697d96d5f76ab14e0caf130769adf78955fcaf3</cites><orcidid>0000-0003-2155-0901</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32263131$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Peng, Lu</creatorcontrib><creatorcontrib>Gao, Meng</creatorcontrib><creatorcontrib>Cai, Xiaolei</creatorcontrib><creatorcontrib>Zhang, Ruoyu</creatorcontrib><creatorcontrib>Li, Kai</creatorcontrib><creatorcontrib>Feng, Guangxue</creatorcontrib><creatorcontrib>Tong, Aijun</creatorcontrib><creatorcontrib>Liu, Bin</creatorcontrib><title>A fluorescent light-up probe based on AIE and ESIPT processes for β-galactosidase activity detection and visualization in living cells</title><title>Journal of materials chemistry. B, Materials for biology and medicine</title><addtitle>J Mater Chem B</addtitle><description>A novel fluorescent probe SA-βGal is reported here with light-up response to β-galactosidase. SA-βGal possesses the β-galactopyranoside group to react with β-galactosidase and releases the fluorescent salicylaldehyde azine with both aggregation induced emission (AIE) and excited-state intramolecular proton transfer (ESIPT) characteristics. The linear fluorescent response enables the in vitro quantification of β-galactosidase activity in a range of 0-0.1 U mL
with a detection limit of 0.014 U mL
. The probe exhibits significant advantages, such as no self-quenching at high concentrations, a large Stokes shift (190 nm) and high specificity to β-galactosidase with an excellent light-up ratio of 820 fold. Moreover, thanks to its good retention in living cells, the application of SA-βGal for the imaging of cellular β-galactosidase was also achieved with high contrast.</description><issn>2050-750X</issn><issn>2050-7518</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNo9UNtKw0AQXUSxUvviB8g-ihDdzWSTzWMsVQsFBSv4FjZ7qStpUrNJof6A_-OH-E1u2tp5mcPMOXM5CF1QckMJpLeStQWhKXBxhM5CwkiQMMqPD5i8DdDIuQ_ig9OYQ3SKBhCGMVCgZ-g7w6bs6kY7qasWl3bx3gbdCq-autC4EE4rXFc4m06wqBSevEyf531Taue0w6Zu8O9PsBClkG3trPIC7KFd23aDlW61x17fa9fWdaK0X2JbsZVftrbVAktdlu4cnRhROj3a5yF6vZ_Mx4_B7OlhOs5mgYSQt4FUiTJFCoxTgAIikiqZUAmRjtNEpbFiJolFQSNNpDAUSBKnQpmEp4wZX4EhutrN9T98dtq1-dK6_gJR6bpzeQg8iVkIIfXU6x1VNrVzjTb5qrFL0WxySvLe-3zM5ndb7zNPvtzP7YqlVgfqv9PwB8AugTY</recordid><startdate>20150101</startdate><enddate>20150101</enddate><creator>Peng, Lu</creator><creator>Gao, Meng</creator><creator>Cai, Xiaolei</creator><creator>Zhang, Ruoyu</creator><creator>Li, Kai</creator><creator>Feng, Guangxue</creator><creator>Tong, Aijun</creator><creator>Liu, Bin</creator><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-2155-0901</orcidid></search><sort><creationdate>20150101</creationdate><title>A fluorescent light-up probe based on AIE and ESIPT processes for β-galactosidase activity detection and visualization in living cells</title><author>Peng, Lu ; Gao, Meng ; Cai, Xiaolei ; Zhang, Ruoyu ; Li, Kai ; Feng, Guangxue ; Tong, Aijun ; Liu, Bin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c328t-cd7dfb9358133b3409dc71c34e697d96d5f76ab14e0caf130769adf78955fcaf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Peng, Lu</creatorcontrib><creatorcontrib>Gao, Meng</creatorcontrib><creatorcontrib>Cai, Xiaolei</creatorcontrib><creatorcontrib>Zhang, Ruoyu</creatorcontrib><creatorcontrib>Li, Kai</creatorcontrib><creatorcontrib>Feng, Guangxue</creatorcontrib><creatorcontrib>Tong, Aijun</creatorcontrib><creatorcontrib>Liu, Bin</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of materials chemistry. B, Materials for biology and medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Peng, Lu</au><au>Gao, Meng</au><au>Cai, Xiaolei</au><au>Zhang, Ruoyu</au><au>Li, Kai</au><au>Feng, Guangxue</au><au>Tong, Aijun</au><au>Liu, Bin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A fluorescent light-up probe based on AIE and ESIPT processes for β-galactosidase activity detection and visualization in living cells</atitle><jtitle>Journal of materials chemistry. B, Materials for biology and medicine</jtitle><addtitle>J Mater Chem B</addtitle><date>2015-01-01</date><risdate>2015</risdate><volume>3</volume><issue>47</issue><spage>9168</spage><epage>9172</epage><pages>9168-9172</pages><issn>2050-750X</issn><eissn>2050-7518</eissn><abstract>A novel fluorescent probe SA-βGal is reported here with light-up response to β-galactosidase. SA-βGal possesses the β-galactopyranoside group to react with β-galactosidase and releases the fluorescent salicylaldehyde azine with both aggregation induced emission (AIE) and excited-state intramolecular proton transfer (ESIPT) characteristics. The linear fluorescent response enables the in vitro quantification of β-galactosidase activity in a range of 0-0.1 U mL
with a detection limit of 0.014 U mL
. The probe exhibits significant advantages, such as no self-quenching at high concentrations, a large Stokes shift (190 nm) and high specificity to β-galactosidase with an excellent light-up ratio of 820 fold. Moreover, thanks to its good retention in living cells, the application of SA-βGal for the imaging of cellular β-galactosidase was also achieved with high contrast.</abstract><cop>England</cop><pmid>32263131</pmid><doi>10.1039/c5tb01938a</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0003-2155-0901</orcidid></addata></record> |
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title | A fluorescent light-up probe based on AIE and ESIPT processes for β-galactosidase activity detection and visualization in living cells |
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