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用于使用 SPR 研究胆固醇-蛋白质相互作用的胆固醇芯片。

Cholesterol Chip for the Study of Cholesterol-Protein Interactions Using SPR.

机构信息

Department of Chemistry and Chemical Biology, Rensselaer Polytechnic Institute, Troy, NY 12180, USA.

Center for Biotechnology and Interdisciplinary Studies, Rensselaer Polytechnic Institute, Troy, NY 12180, USA.

出版信息

Biosensors (Basel). 2022 Sep 25;12(10):788. doi: 10.3390/bios12100788.

DOI:10.3390/bios12100788
PMID:36290926
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9599816/
Abstract

Cholesterol, an important lipid in animal membranes, binds to hydrophobic pockets within many soluble proteins, transport proteins and membrane bound proteins. The study of cholesterol-protein interactions in aqueous solutions is complicated by cholesterol's low solubility and often requires organic co-solvents or surfactant additives. We report the synthesis of a biotinylated cholesterol and immobilization of this derivative on a streptavidin chip. Surface plasmon resonance (SPR) was then used to measure the kinetics of cholesterol interaction with cholesterol-binding proteins, hedgehog protein and tyrosine phosphatase 1B.

摘要

胆固醇是动物膜中的一种重要脂质,它与许多可溶性蛋白、转运蛋白和膜结合蛋白中的疏水口袋结合。在水溶液中研究胆固醇-蛋白质相互作用比较复杂,因为胆固醇的溶解度低,通常需要有机溶剂或表面活性剂添加剂。我们报告了一种生物素化胆固醇的合成,并将该衍生物固定在链霉亲和素芯片上。然后,表面等离子体共振(SPR)用于测量胆固醇与胆固醇结合蛋白、 hedgehog 蛋白和酪氨酸磷酸酶 1B 相互作用的动力学。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af17/9599816/c73d8ebcb6e4/biosensors-12-00788-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af17/9599816/0eecd410fa3d/biosensors-12-00788-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af17/9599816/09220bc45d0b/biosensors-12-00788-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af17/9599816/d43cd0f5777a/biosensors-12-00788-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af17/9599816/2780c98cd7e9/biosensors-12-00788-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af17/9599816/c73d8ebcb6e4/biosensors-12-00788-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af17/9599816/0eecd410fa3d/biosensors-12-00788-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af17/9599816/09220bc45d0b/biosensors-12-00788-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af17/9599816/d43cd0f5777a/biosensors-12-00788-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af17/9599816/2780c98cd7e9/biosensors-12-00788-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af17/9599816/c73d8ebcb6e4/biosensors-12-00788-g005.jpg

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Cholesterol: Bioactivities, Structural Modification, Mechanisms of Action, and Structure-Activity Relationships.胆固醇:生物活性、结构修饰、作用机制和构效关系。
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Influence of fluorophore and linker length on the localization and trafficking of fluorescent sterol probes.
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Preferred Endocytosis of Amyloid Precursor Protein from Cholesterol-Enriched Lipid Raft Microdomains.优先从富含胆固醇的脂筏微域内摄取淀粉样前体蛋白。
Molecules. 2020 Nov 24;25(23):5490. doi: 10.3390/molecules25235490.
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Characterization of heparin and severe acute respiratory syndrome-related coronavirus 2 (SARS-CoV-2) spike glycoprotein binding interactions.肝素与严重急性呼吸综合征相关冠状病毒 2(SARS-CoV-2)刺突糖蛋白结合相互作用的表征。
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