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用于治疗用途的重组蛋白脂质体的生产。

Production of recombinant proteoliposomes for therapeutic uses.

作者信息

Liguori Lavinia, Lenormand Jean Luc

机构信息

HumProTher Laboratory, TIMC-ThereX, UMR 5525 CNRS-UJF, Université Joseph Fourier, UFR de Médecine, Domaine de la Merci, La Tronche, France.

出版信息

Methods Enzymol. 2009;465:209-23. doi: 10.1016/S0076-6879(09)65011-4.

Abstract

One of the major challenges in human therapy is to develop delivery systems that are convenient and effective for tackling problems in disease treatments. In the past 20 years, liposomes have represented promising pharmaceutical carriers for drug delivery. Due to their biophysical properties, liposomes can deliver and specifically target a large set of bioactive molecules, they can protect molecules from degradation, and their composition is easily modifiable. The use of recombinant proteoliposomes containing therapeutic membrane proteins is a recently developed technology that allows biologically active proteins to penetrate across the plasma membrane of eukaryotic cells. One of the bottlenecks in this powerful delivery system lies in the production of functional therapeutic membrane proteins mainly due to their biophysical characteristics. Membrane proteins represent about 30% of the total proteins from an organism, and play a central role in drug discovery as potential pharmaceutical targets. This chapter describes the methodology for the production of bioactive proteoliposomes containing therapeutic, proapoptotic membrane proteins synthesized with an optimized cell-free expression system. We will examine (1) the design of the expression vectors and the liposome compositions compatible with the cell-free expression system; (2) the production of membrane proteins using a cell-free expression system in combination with liposomes, to obtain in a one-step reaction functional therapeutic proteoliposomes; (3) proteoliposome purification for further use in the treatment of cancer cells; and (4) the methodology for detecting apoptosis in cells after treatment. Furthermore, this system can be easily adapted for producing "difficult to express proteins" compared with the classical overexpression (bacterial or eukaryotic) systems.

摘要

人类治疗中的主要挑战之一是开发方便且有效的给药系统,以解决疾病治疗中的问题。在过去20年中,脂质体已成为药物递送方面很有前景的药物载体。由于其生物物理特性,脂质体可以递送并特异性靶向大量生物活性分子,它们可以保护分子不被降解,并且其组成易于修饰。使用含有治疗性膜蛋白的重组蛋白脂质体是一项最近开发的技术,它能使生物活性蛋白穿透真核细胞的质膜。这个强大的递送系统的瓶颈之一在于功能性治疗性膜蛋白的生产,这主要是由于它们的生物物理特性。膜蛋白约占生物体总蛋白的30%,作为潜在的药物靶点,在药物发现中起着核心作用。本章描述了用优化的无细胞表达系统合成含有治疗性促凋亡膜蛋白的生物活性蛋白脂质体的方法。我们将研究:(1)与无细胞表达系统兼容的表达载体和脂质体组成的设计;(2)使用无细胞表达系统结合脂质体生产膜蛋白,以在一步反应中获得功能性治疗性蛋白脂质体;(3)蛋白脂质体的纯化,以便进一步用于癌细胞治疗;以及(4)处理后检测细胞凋亡的方法。此外,与经典的过表达(细菌或真核)系统相比,该系统可以很容易地用于生产“难以表达的蛋白”。

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