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通过带有新型荧光自由基标签的液相色谱-荧光检测-高分辨质谱联用技术对糖链进行灵敏的荧光定量和高效的自由基表征

Sensitive Fluorescence Quantitation and Efficient Free Radical Characterization of -Glycans via LC-FLR-HRMS/MS with a Novel Fluorescent Free Radical Tag.

作者信息

Murtada Rayan, Szafranski C J, Tevletidis Maria, Finn Shane, Gilles Wilthon, Tahsin Tabia, Gao Jinshan

机构信息

Department of Chemistry and Biochemistry, Montclair State University, 1 Normal Avenue, Montclair, New Jersey 07043, United States.

Sokol Institute of Pharmaceutical Life Sciences, Montclair, New Jersey 07043, United States.

出版信息

Anal Chem. 2025 Apr 8;97(13):7118-7127. doi: 10.1021/acs.analchem.4c06294. Epub 2025 Mar 25.

DOI:10.1021/acs.analchem.4c06294
PMID:40129309
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11983377/
Abstract

Glycans are some of the most difficult biomolecules to analyze owing to their branching tendencies as well as their regiochemical and stereochemical diversity. Yet, the correlation between various pathological states and glycan quantity or structural alterations has demonstrated the importance and urgency for the development of a more robust glycan analytical technique. Furthermore, the manufacturing and regulation of biopharmaceuticals demands a feasible and improved analytical approach toward the characterization and quantitation of glycosylations. Unfortunately, multiple commercially available glycan tags lack, in combination, liquid chromatography detection sensitivity, chemical stability and, most importantly, optimal glycan characterization capabilities. Therefore, a novel fluorescent tag coupled with a free radical approach for glycan characterization was designed and developed to help address this gap in glycan analysis. The analytical capabilities of this novel tag were assessed via hydrophilic liquid chromatography-fluorescence quantitation and ESI/MS free radical-mediated characterization by using linear glycan standards, branched isobaric glycans lacto--difucohexaose I and lacto--difucohexaose II, and -glycans released from ribonuclease B.

摘要

由于聚糖具有分支倾向以及区域化学和立体化学多样性,它们是最难分析的生物分子之一。然而,各种病理状态与聚糖数量或结构改变之间的相关性表明,开发更强大的聚糖分析技术具有重要性和紧迫性。此外,生物制药的生产和监管需要一种可行且改进的分析方法来表征和定量糖基化。不幸的是,多种市售的聚糖标签在液相色谱检测灵敏度、化学稳定性以及最重要的最佳聚糖表征能力方面存在综合不足。因此,设计并开发了一种结合自由基方法用于聚糖表征的新型荧光标签,以帮助填补聚糖分析中的这一空白。通过亲水液相色谱 - 荧光定量以及电喷雾电离/质谱自由基介导的表征,使用线性聚糖标准品、支链等压聚糖乳糖 - 二岩藻糖六糖I和乳糖 - 二岩藻糖六糖II以及从核糖核酸酶B释放的聚糖来评估这种新型标签的分析能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84f5/11983377/1e77037e042a/ac4c06294_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84f5/11983377/909e3a91fc83/ac4c06294_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84f5/11983377/afa4a1ae1b6b/ac4c06294_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84f5/11983377/d2f06113e205/ac4c06294_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84f5/11983377/eff6789d78c3/ac4c06294_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84f5/11983377/3c952e32cd44/ac4c06294_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84f5/11983377/1e77037e042a/ac4c06294_0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84f5/11983377/909e3a91fc83/ac4c06294_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84f5/11983377/afa4a1ae1b6b/ac4c06294_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84f5/11983377/d2f06113e205/ac4c06294_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84f5/11983377/eff6789d78c3/ac4c06294_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84f5/11983377/3c952e32cd44/ac4c06294_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/84f5/11983377/1e77037e042a/ac4c06294_0006.jpg

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