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Hydrophilic, dual amino acid–functionalized zinc sulfide quantum dot for specific identification of N‐glycopeptides from biological samples
Rationale Glycosylation of proteins is one of the most significant and complex post‐translational modifications, and N‐glycosylation plays a crucial role in life activities. Mass spectrometry (MS) has been a powerful technique in the analysis of protein glycosylation. However, the direct detection o...
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Published in: | Rapid communications in mass spectrometry 2022-12, Vol.36 (24), p.e9405-n/a |
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creator | Feng, Quanshou Xie, Zehu Liang, Hongze Zhang, Zhenbin Yan, Yinghua Ding, Chuan‐Fan |
description | Rationale
Glycosylation of proteins is one of the most significant and complex post‐translational modifications, and N‐glycosylation plays a crucial role in life activities. Mass spectrometry (MS) has been a powerful technique in the analysis of protein glycosylation. However, the direct detection of glycoproteins in biological samples based on MS still suffers from huge challenges. Therefore, enrichment and purification of samples before MS analysis is an essential prerequisite.
Methods
Hydrophilic interaction liquid chromatography (HILIC) has significantly developed for selective enrichment of glycopeptides due to its simple operation process and unbiased enrichment. Herein, hydrophilic, dual amino acid–functionalized zinc sulfide quantum dots (ZnS QDs) were prepared to enrich glycopeptides using an easy procedure. The enriched glycopeptides were detected using matrix‐assisted laser desorption ionization time‐of‐flight mass spectrometry (MALDI‐TOF MS).
Results
The obtained material exhibited high selectivity (1:2000), low detection limit (0.1 fmol/μl), good repeatability (10 times), and excellent recovery (89.8%) in glycopeptide enrichment. In the actual application in biological samples, 71 N‐glycopeptides and 161 N‐glycopeptides were detected from human saliva and serum, respectively.
Conclusions
ZnS‐Au‐GC was successfully prepared using an easy method. The results showed that the obtained material exhibited excellent performance in glycopeptide enrichment. Furthermore, it had showed great potential for glycopeptide enrichment in complex biological samples. |
doi_str_mv | 10.1002/rcm.9405 |
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Glycosylation of proteins is one of the most significant and complex post‐translational modifications, and N‐glycosylation plays a crucial role in life activities. Mass spectrometry (MS) has been a powerful technique in the analysis of protein glycosylation. However, the direct detection of glycoproteins in biological samples based on MS still suffers from huge challenges. Therefore, enrichment and purification of samples before MS analysis is an essential prerequisite.
Methods
Hydrophilic interaction liquid chromatography (HILIC) has significantly developed for selective enrichment of glycopeptides due to its simple operation process and unbiased enrichment. Herein, hydrophilic, dual amino acid–functionalized zinc sulfide quantum dots (ZnS QDs) were prepared to enrich glycopeptides using an easy procedure. The enriched glycopeptides were detected using matrix‐assisted laser desorption ionization time‐of‐flight mass spectrometry (MALDI‐TOF MS).
Results
The obtained material exhibited high selectivity (1:2000), low detection limit (0.1 fmol/μl), good repeatability (10 times), and excellent recovery (89.8%) in glycopeptide enrichment. In the actual application in biological samples, 71 N‐glycopeptides and 161 N‐glycopeptides were detected from human saliva and serum, respectively.
Conclusions
ZnS‐Au‐GC was successfully prepared using an easy method. The results showed that the obtained material exhibited excellent performance in glycopeptide enrichment. Furthermore, it had showed great potential for glycopeptide enrichment in complex biological samples.</description><identifier>ISSN: 0951-4198</identifier><identifier>EISSN: 1097-0231</identifier><identifier>DOI: 10.1002/rcm.9405</identifier><language>eng</language><publisher>Bognor Regis: Wiley Subscription Services, Inc</publisher><subject>Amino acids ; Antibiotics ; Biological properties ; Enrichment ; Glycopeptides ; Glycoproteins ; Hydrophilicity ; Liquid chromatography ; Mass spectrometry ; Proteins ; Quantum dots ; Scientific imaging ; Selectivity ; Spectroscopy ; Zinc sulfide</subject><ispartof>Rapid communications in mass spectrometry, 2022-12, Vol.36 (24), p.e9405-n/a</ispartof><rights>2022 John Wiley & Sons Ltd.</rights><rights>2022 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3265-8f67f3e911743e2f6b34c400a038c37a207097810d313ea7024e530bd74c89f83</citedby><cites>FETCH-LOGICAL-c3265-8f67f3e911743e2f6b34c400a038c37a207097810d313ea7024e530bd74c89f83</cites><orcidid>0000-0002-0569-2881</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></links><search><creatorcontrib>Feng, Quanshou</creatorcontrib><creatorcontrib>Xie, Zehu</creatorcontrib><creatorcontrib>Liang, Hongze</creatorcontrib><creatorcontrib>Zhang, Zhenbin</creatorcontrib><creatorcontrib>Yan, Yinghua</creatorcontrib><creatorcontrib>Ding, Chuan‐Fan</creatorcontrib><title>Hydrophilic, dual amino acid–functionalized zinc sulfide quantum dot for specific identification of N‐glycopeptides from biological samples</title><title>Rapid communications in mass spectrometry</title><description>Rationale
Glycosylation of proteins is one of the most significant and complex post‐translational modifications, and N‐glycosylation plays a crucial role in life activities. Mass spectrometry (MS) has been a powerful technique in the analysis of protein glycosylation. However, the direct detection of glycoproteins in biological samples based on MS still suffers from huge challenges. Therefore, enrichment and purification of samples before MS analysis is an essential prerequisite.
Methods
Hydrophilic interaction liquid chromatography (HILIC) has significantly developed for selective enrichment of glycopeptides due to its simple operation process and unbiased enrichment. Herein, hydrophilic, dual amino acid–functionalized zinc sulfide quantum dots (ZnS QDs) were prepared to enrich glycopeptides using an easy procedure. The enriched glycopeptides were detected using matrix‐assisted laser desorption ionization time‐of‐flight mass spectrometry (MALDI‐TOF MS).
Results
The obtained material exhibited high selectivity (1:2000), low detection limit (0.1 fmol/μl), good repeatability (10 times), and excellent recovery (89.8%) in glycopeptide enrichment. In the actual application in biological samples, 71 N‐glycopeptides and 161 N‐glycopeptides were detected from human saliva and serum, respectively.
Conclusions
ZnS‐Au‐GC was successfully prepared using an easy method. The results showed that the obtained material exhibited excellent performance in glycopeptide enrichment. Furthermore, it had showed great potential for glycopeptide enrichment in complex biological samples.</description><subject>Amino acids</subject><subject>Antibiotics</subject><subject>Biological properties</subject><subject>Enrichment</subject><subject>Glycopeptides</subject><subject>Glycoproteins</subject><subject>Hydrophilicity</subject><subject>Liquid chromatography</subject><subject>Mass spectrometry</subject><subject>Proteins</subject><subject>Quantum dots</subject><subject>Scientific imaging</subject><subject>Selectivity</subject><subject>Spectroscopy</subject><subject>Zinc sulfide</subject><issn>0951-4198</issn><issn>1097-0231</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNp10c1KAzEQB_AgCtYq-AgBLx7cOtlkv45S1ApVQfS8pNmkpmQ322QXaU99AwXfsE_irhUEwdME5peBmT9CpwRGBCC8dKIcZQyiPTQgkCUBhJTsowFkEQkYydJDdOT9AoCQKIQBep-sCmfrV220uMBFyw3mpa4s5kIX282naivRaFtxo9eywGtdCexbo3Qh8bLlVdOWuLANVtZhX0uhlRa4a1ZN_-L9V2wVfthuPuZmJWwt66Zre6ycLfFMW2PnnTPY87I20h-jA8WNlyc_dYhebq6fx5Ng-nh7N76aBoKGcRSkKk4UlRkhCaMyVPGMMsEAONBU0ISHkHTLpwQKSqjkCYRMRhRmRcJEmqmUDtH5bm7t7LKVvslL7YU0hlfStj4PE5LGlGYZ6-jZH7qwresu0ivKYkIgjn4HCme9d1LltdMld6ucQN4nk3fJ5H0yHQ129E0bufrX5U_j-2__BbEQkqI</recordid><startdate>20221230</startdate><enddate>20221230</enddate><creator>Feng, Quanshou</creator><creator>Xie, Zehu</creator><creator>Liang, Hongze</creator><creator>Zhang, Zhenbin</creator><creator>Yan, Yinghua</creator><creator>Ding, Chuan‐Fan</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>JQ2</scope><scope>L7M</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-0569-2881</orcidid></search><sort><creationdate>20221230</creationdate><title>Hydrophilic, dual amino acid–functionalized zinc sulfide quantum dot for specific identification of N‐glycopeptides from biological samples</title><author>Feng, Quanshou ; Xie, Zehu ; Liang, Hongze ; Zhang, Zhenbin ; Yan, Yinghua ; Ding, Chuan‐Fan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3265-8f67f3e911743e2f6b34c400a038c37a207097810d313ea7024e530bd74c89f83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Amino acids</topic><topic>Antibiotics</topic><topic>Biological properties</topic><topic>Enrichment</topic><topic>Glycopeptides</topic><topic>Glycoproteins</topic><topic>Hydrophilicity</topic><topic>Liquid chromatography</topic><topic>Mass spectrometry</topic><topic>Proteins</topic><topic>Quantum dots</topic><topic>Scientific imaging</topic><topic>Selectivity</topic><topic>Spectroscopy</topic><topic>Zinc sulfide</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Feng, Quanshou</creatorcontrib><creatorcontrib>Xie, Zehu</creatorcontrib><creatorcontrib>Liang, Hongze</creatorcontrib><creatorcontrib>Zhang, Zhenbin</creatorcontrib><creatorcontrib>Yan, Yinghua</creatorcontrib><creatorcontrib>Ding, Chuan‐Fan</creatorcontrib><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>ProQuest Computer Science Collection</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Rapid communications in mass spectrometry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Feng, Quanshou</au><au>Xie, Zehu</au><au>Liang, Hongze</au><au>Zhang, Zhenbin</au><au>Yan, Yinghua</au><au>Ding, Chuan‐Fan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hydrophilic, dual amino acid–functionalized zinc sulfide quantum dot for specific identification of N‐glycopeptides from biological samples</atitle><jtitle>Rapid communications in mass spectrometry</jtitle><date>2022-12-30</date><risdate>2022</risdate><volume>36</volume><issue>24</issue><spage>e9405</spage><epage>n/a</epage><pages>e9405-n/a</pages><issn>0951-4198</issn><eissn>1097-0231</eissn><abstract>Rationale
Glycosylation of proteins is one of the most significant and complex post‐translational modifications, and N‐glycosylation plays a crucial role in life activities. Mass spectrometry (MS) has been a powerful technique in the analysis of protein glycosylation. However, the direct detection of glycoproteins in biological samples based on MS still suffers from huge challenges. Therefore, enrichment and purification of samples before MS analysis is an essential prerequisite.
Methods
Hydrophilic interaction liquid chromatography (HILIC) has significantly developed for selective enrichment of glycopeptides due to its simple operation process and unbiased enrichment. Herein, hydrophilic, dual amino acid–functionalized zinc sulfide quantum dots (ZnS QDs) were prepared to enrich glycopeptides using an easy procedure. The enriched glycopeptides were detected using matrix‐assisted laser desorption ionization time‐of‐flight mass spectrometry (MALDI‐TOF MS).
Results
The obtained material exhibited high selectivity (1:2000), low detection limit (0.1 fmol/μl), good repeatability (10 times), and excellent recovery (89.8%) in glycopeptide enrichment. In the actual application in biological samples, 71 N‐glycopeptides and 161 N‐glycopeptides were detected from human saliva and serum, respectively.
Conclusions
ZnS‐Au‐GC was successfully prepared using an easy method. The results showed that the obtained material exhibited excellent performance in glycopeptide enrichment. Furthermore, it had showed great potential for glycopeptide enrichment in complex biological samples.</abstract><cop>Bognor Regis</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/rcm.9405</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-0569-2881</orcidid></addata></record> |
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subjects | Amino acids Antibiotics Biological properties Enrichment Glycopeptides Glycoproteins Hydrophilicity Liquid chromatography Mass spectrometry Proteins Quantum dots Scientific imaging Selectivity Spectroscopy Zinc sulfide |
title | Hydrophilic, dual amino acid–functionalized zinc sulfide quantum dot for specific identification of N‐glycopeptides from biological samples |
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