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Background-free cell surface glycan analysis using persistent luminescence nanoparticle as an optical probe
In this work, we report a novel cell surface glycan analysis method based on persistent luminescence nanoparticle (PLNP) ZnGa2O4: Cr3+ (ZGC) as an optical probe. ZGC was first silanized by (3-Aminopropyl) triethoxysilane (APTES), followed by PEGylation with NHS-P EG-Biotin, which not only introduces...
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Published in: | Analytical biochemistry 2020-07, Vol.601, p.113780, Article 113780 |
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description | In this work, we report a novel cell surface glycan analysis method based on persistent luminescence nanoparticle (PLNP) ZnGa2O4: Cr3+ (ZGC) as an optical probe. ZGC was first silanized by (3-Aminopropyl) triethoxysilane (APTES), followed by PEGylation with NHS-P EG-Biotin, which not only introduces biotin, but significantly improves the dispersibility and stability of the nanoparticles. Neutral-avidin was then coupled on ZGC surface through the specific biotin-avidin interaction, producing a ZGC-PEG-avidin nanoprobe. As for cell surface glycan detection, different surface glycans are recognized with their corresponding biotinylated lectins, which are then traced by ZGC-PEG-avidin. The persistent luminescence signal is recorded by a microtiter plate reader in time-resolved fluorescence mode. Glycans expression profiling on prostate cancer cell DU145 and normal prostate cell RWPE-1 was analyzed by the proposed detection platform. Similar results were observed from the conventional horseradish peroxidase (HRP)-catalyzed absorbent assay and confocal microscope-based fluorescence imaging, demonstrating the applicability of the proposed platform. The approach based on the long afterglow property of ZGC efficiently eliminates the background noise from cells and substrate, resulting in the best signal-to-noise ratio and high detection sensitivity.
•ZGC-PEG-Biotin with good dispersibility and persistent luminescence is synthesized by PEGylation.•A background-free analytical platform is developed with ZGC as an optical nanoprobe.•Glycan expression profiling on cancer and normal cell surface was analyzed by the proposed platform. |
doi_str_mv | 10.1016/j.ab.2020.113780 |
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•ZGC-PEG-Biotin with good dispersibility and persistent luminescence is synthesized by PEGylation.•A background-free analytical platform is developed with ZGC as an optical nanoprobe.•Glycan expression profiling on cancer and normal cell surface was analyzed by the proposed platform.</description><identifier>ISSN: 0003-2697</identifier><identifier>EISSN: 1096-0309</identifier><identifier>DOI: 10.1016/j.ab.2020.113780</identifier><identifier>PMID: 32470346</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Background-free analysis ; Cell surface glycans ; Cells, Cultured ; Humans ; Lectins ; Luminescence ; Luminescent Agents - chemistry ; Nanoparticles - chemistry ; Optical Imaging ; Persistent luminescence nanoparticles ; Polysaccharides - analysis</subject><ispartof>Analytical biochemistry, 2020-07, Vol.601, p.113780, Article 113780</ispartof><rights>2020 Elsevier Inc.</rights><rights>Copyright © 2020 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c350t-914667d07baa979a883049d379fa24322a02b772f747344d8d5a709709eed3943</citedby><cites>FETCH-LOGICAL-c350t-914667d07baa979a883049d379fa24322a02b772f747344d8d5a709709eed3943</cites></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/32470346$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>He, Na</creatorcontrib><creatorcontrib>Jiang, Ying</creatorcontrib><creatorcontrib>Lei, Lingli</creatorcontrib><creatorcontrib>Liu, Yingshuai</creatorcontrib><title>Background-free cell surface glycan analysis using persistent luminescence nanoparticle as an optical probe</title><title>Analytical biochemistry</title><addtitle>Anal Biochem</addtitle><description>In this work, we report a novel cell surface glycan analysis method based on persistent luminescence nanoparticle (PLNP) ZnGa2O4: Cr3+ (ZGC) as an optical probe. ZGC was first silanized by (3-Aminopropyl) triethoxysilane (APTES), followed by PEGylation with NHS-P EG-Biotin, which not only introduces biotin, but significantly improves the dispersibility and stability of the nanoparticles. Neutral-avidin was then coupled on ZGC surface through the specific biotin-avidin interaction, producing a ZGC-PEG-avidin nanoprobe. As for cell surface glycan detection, different surface glycans are recognized with their corresponding biotinylated lectins, which are then traced by ZGC-PEG-avidin. The persistent luminescence signal is recorded by a microtiter plate reader in time-resolved fluorescence mode. Glycans expression profiling on prostate cancer cell DU145 and normal prostate cell RWPE-1 was analyzed by the proposed detection platform. Similar results were observed from the conventional horseradish peroxidase (HRP)-catalyzed absorbent assay and confocal microscope-based fluorescence imaging, demonstrating the applicability of the proposed platform. The approach based on the long afterglow property of ZGC efficiently eliminates the background noise from cells and substrate, resulting in the best signal-to-noise ratio and high detection sensitivity.
•ZGC-PEG-Biotin with good dispersibility and persistent luminescence is synthesized by PEGylation.•A background-free analytical platform is developed with ZGC as an optical nanoprobe.•Glycan expression profiling on cancer and normal cell surface was analyzed by the proposed platform.</description><subject>Background-free analysis</subject><subject>Cell surface glycans</subject><subject>Cells, Cultured</subject><subject>Humans</subject><subject>Lectins</subject><subject>Luminescence</subject><subject>Luminescent Agents - chemistry</subject><subject>Nanoparticles - chemistry</subject><subject>Optical Imaging</subject><subject>Persistent luminescence nanoparticles</subject><subject>Polysaccharides - analysis</subject><issn>0003-2697</issn><issn>1096-0309</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp1kM1rGzEQxUVJaZy0956C_oF1Rh9eWbk1If2AQC_tWcxKs0bOWrtIuwX_95Fxk1tgYHjwfo-Zx9hXAWsBor3dr7FbS5BVCmW28IGtBNi2AQX2gq0AQDWyteaSXZWyBxBCb9pP7FJJbUDpdsWe79E_7_K4pND0mYh7GgZeltyjJ74bjh4Tx4TDscTClxLTjk-Uq5gpzXxYDjFR8ZSqO2EaJ8xz9ANxLBXj41QVDnzKY0ef2cceh0Jf_u9r9vf745-Hn83T7x-_Hr49NV5tYG6s0G1rApgO0RqL260CbYMytkeplZQIsjNG9kYbpXXYhg0asHWIgrJaXTM45_o8lpKpd1OOB8xHJ8CdenN7h5079ebOvVXk5oxMS3eg8Aa8FlUNd2cD1cP_Rcqu-Hj6OsRMfnZhjO-nvwDI4n2Q</recordid><startdate>20200715</startdate><enddate>20200715</enddate><creator>He, Na</creator><creator>Jiang, Ying</creator><creator>Lei, Lingli</creator><creator>Liu, Yingshuai</creator><general>Elsevier Inc</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></search><sort><creationdate>20200715</creationdate><title>Background-free cell surface glycan analysis using persistent luminescence nanoparticle as an optical probe</title><author>He, Na ; Jiang, Ying ; Lei, Lingli ; Liu, Yingshuai</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c350t-914667d07baa979a883049d379fa24322a02b772f747344d8d5a709709eed3943</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Background-free analysis</topic><topic>Cell surface glycans</topic><topic>Cells, Cultured</topic><topic>Humans</topic><topic>Lectins</topic><topic>Luminescence</topic><topic>Luminescent Agents - chemistry</topic><topic>Nanoparticles - chemistry</topic><topic>Optical Imaging</topic><topic>Persistent luminescence nanoparticles</topic><topic>Polysaccharides - analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>He, Na</creatorcontrib><creatorcontrib>Jiang, Ying</creatorcontrib><creatorcontrib>Lei, Lingli</creatorcontrib><creatorcontrib>Liu, Yingshuai</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Analytical biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>He, Na</au><au>Jiang, Ying</au><au>Lei, Lingli</au><au>Liu, Yingshuai</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Background-free cell surface glycan analysis using persistent luminescence nanoparticle as an optical probe</atitle><jtitle>Analytical biochemistry</jtitle><addtitle>Anal Biochem</addtitle><date>2020-07-15</date><risdate>2020</risdate><volume>601</volume><spage>113780</spage><pages>113780-</pages><artnum>113780</artnum><issn>0003-2697</issn><eissn>1096-0309</eissn><abstract>In this work, we report a novel cell surface glycan analysis method based on persistent luminescence nanoparticle (PLNP) ZnGa2O4: Cr3+ (ZGC) as an optical probe. ZGC was first silanized by (3-Aminopropyl) triethoxysilane (APTES), followed by PEGylation with NHS-P EG-Biotin, which not only introduces biotin, but significantly improves the dispersibility and stability of the nanoparticles. Neutral-avidin was then coupled on ZGC surface through the specific biotin-avidin interaction, producing a ZGC-PEG-avidin nanoprobe. As for cell surface glycan detection, different surface glycans are recognized with their corresponding biotinylated lectins, which are then traced by ZGC-PEG-avidin. The persistent luminescence signal is recorded by a microtiter plate reader in time-resolved fluorescence mode. Glycans expression profiling on prostate cancer cell DU145 and normal prostate cell RWPE-1 was analyzed by the proposed detection platform. Similar results were observed from the conventional horseradish peroxidase (HRP)-catalyzed absorbent assay and confocal microscope-based fluorescence imaging, demonstrating the applicability of the proposed platform. The approach based on the long afterglow property of ZGC efficiently eliminates the background noise from cells and substrate, resulting in the best signal-to-noise ratio and high detection sensitivity.
•ZGC-PEG-Biotin with good dispersibility and persistent luminescence is synthesized by PEGylation.•A background-free analytical platform is developed with ZGC as an optical nanoprobe.•Glycan expression profiling on cancer and normal cell surface was analyzed by the proposed platform.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>32470346</pmid><doi>10.1016/j.ab.2020.113780</doi></addata></record> |
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subjects | Background-free analysis Cell surface glycans Cells, Cultured Humans Lectins Luminescence Luminescent Agents - chemistry Nanoparticles - chemistry Optical Imaging Persistent luminescence nanoparticles Polysaccharides - analysis |
title | Background-free cell surface glycan analysis using persistent luminescence nanoparticle as an optical probe |
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