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用于将蛋白质偶联到预先形成的普通或聚乙二醇化脂质体上的三酰化聚乙二醇甾醇。

Tresylated PEG-sterols for coupling of proteins to preformed plain or PEGylated liposomes.

作者信息

Steenpass Thomas, Lung Andreas, Schubert Rolf

机构信息

Institute of Pharmaceutical Sciences, Department of Pharmaceutical Technology and Biopharmacy, Hermann-Herder-Str. 9, D-79104 Freiburg, Germany.

出版信息

Biochim Biophys Acta. 2006 Jan;1758(1):20-8. doi: 10.1016/j.bbamem.2005.12.010. Epub 2006 Jan 18.

Abstract

A simple and inexpensive method for functionalization of preformed liposomes is presented. Soy sterol-PEG1300 ethers are activated by tresylation at the end of the PEG chain. Coupling of bovine serum albumin as an amino group containing model ligand to the activated lipids can be performed at pH 8.4 with high efficiency. At room temperature, the mixture of sterol-PEG and sterol-PEG-protein inserts rapidly into the outer liposome monolayer with high efficiency (>100 microg protein/mumol total lipid). This method of post-functionalization is shown to be effective with fluid or rigid and plain or pre-PEGylated liposomes (EPC/Chol, 7:3; HSPC/Chol 2:1, and EPC/Chol/MPEG2000-DSPE 2:1:0.16 molar ratios). The release of entrapped calcein upon the insertion of 7.5 mol% of the functionalized sterols is lower than 4%. Incubation of post-functionalized liposomes with serum for 20 h at 37 degrees C shows stable protein attachment at the liposome surface.

摘要

本文介绍了一种简单且廉价的预制脂质体功能化方法。大豆甾醇-聚乙二醇1300醚在聚乙二醇链末端通过三氟甲磺酸酯化被激活。作为含氨基模型配体的牛血清白蛋白与活化脂质的偶联可在pH 8.4下高效进行。在室温下,甾醇-聚乙二醇和甾醇-聚乙二醇-蛋白质的混合物能高效地快速插入脂质体的外层单分子层(>100微克蛋白质/微摩尔总脂质)。这种后功能化方法对流体或刚性、普通或预先聚乙二醇化的脂质体(EPC/胆固醇,7:3;HSPC/胆固醇2:1,以及EPC/胆固醇/MPEG2000-DSPE 2:1:0.16摩尔比)均有效。插入7.5摩尔%功能化甾醇后,包封的钙黄绿素释放率低于4%。将后功能化脂质体在37℃下与血清孵育20小时,结果表明蛋白质在脂质体表面的附着稳定。

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