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细胞质内药物载体递呈的绝对定量。

Absolute Quantification of Drug Vector Delivery to the Cytosol.

机构信息

Cellular and Chemical Biology Unit, U1143 INSERM, UMR3666 CNRS, Institut Curie-, Université PSL, 26 rue d'Ulm, 75248, Paris Cedex 05, France.

Université de Paris, 85 boulevard Saint-Germain, 75006, Paris, France.

出版信息

Angew Chem Int Ed Engl. 2021 Jun 25;60(27):14824-14830. doi: 10.1002/anie.202102332. Epub 2021 May 28.

Abstract

Macromolecular drugs inefficiently cross membranes to reach their cytosolic targets. They require drug delivery vectors to facilitate their translocation across the plasma membrane or escape from endosomes. Optimization of these vectors has however been hindered by the difficulty to accurately measure cytosolic arrival. We have developed an exceptionally sensitive and robust assay for the relative or absolute quantification of this step. The assay is based on benzylguanine and biotin modifications on a drug delivery vector of interest, which allow, respectively, for selective covalent capture in the cytosol with a SNAP-tag fusion protein and for quantification at picomolar sensitivity. The assay was validated by determining the absolute numbers of cytosolic molecules for two drug delivery vectors: the B-subunit of Shiga toxin and the cell-penetrating peptide TAT. We expect this assay to favor delivery vector optimization and the understanding of the enigmatic translocation process.

摘要

大分子药物难以有效穿透细胞膜到达胞质溶胶中的靶标。它们需要药物递送载体来促进其穿过质膜或从内涵体逃逸。然而,这些载体的优化受到难以准确测量胞质溶胶到达的阻碍。我们开发了一种特别灵敏和稳健的测定法,用于相对或绝对定量此步骤。该测定法基于苄基鸟嘌呤和生物素修饰感兴趣的药物递送载体,分别允许与 SNAP 标签融合蛋白在胞质溶胶中进行选择性共价捕获,并以皮摩尔灵敏度进行定量。该测定法通过确定两种药物递送载体的胞质溶胶分子的绝对数量进行了验证:志贺毒素的 B 亚基和细胞穿透肽 TAT。我们期望该测定法有利于递药载体的优化和对神秘的转位过程的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7d9/8252025/18b29dade01d/ANIE-60-14824-g001.jpg

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