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细胞外囊泡作为膜相关治疗性蛋白质递送的平台。

Extracellular vesicles as a platform for membrane-associated therapeutic protein delivery.

作者信息

Yang Yoosoo, Hong Yeonsun, Cho Eunji, Kim Gi Beom, Kim In-San

机构信息

Biomedical Research Institute, Korea Institute of Science and Technology (KIST), Seoul, Republic of Korea.

Division for Bio-Medical Science & Technology, KIST School, Korea University of Science and Technology, Seoul, Republic of Korea.

出版信息

J Extracell Vesicles. 2018 Mar 1;7(1):1440131. doi: 10.1080/20013078.2018.1440131. eCollection 2018.

Abstract

Membrane proteins are of great research interest, particularly because they are rich in targets for therapeutic application. The suitability of various membrane proteins as targets for therapeutic formulations, such as drugs or antibodies, has been studied in preclinical and clinical studies. For therapeutic application, however, a protein must be expressed and purified in as close to its native conformation as possible. This has proven difficult for membrane proteins, as their native conformation requires the association with an appropriate cellular membrane. One solution to this problem is to use extracellular vesicles as a display platform. Exosomes and microvesicles are membranous extracellular vesicles that are released from most cells. Their membranes may provide a favourable microenvironment for membrane proteins to take on their proper conformation, activity, and membrane distribution; moreover, membrane proteins can cluster into microdomains on the surface of extracellular vesicles following their biogenesis. In this review, we survey the state-of-the-art of extracellular vesicle (exosome and small-sized microvesicle)-based therapeutics, evaluate the current biological understanding of these formulations, and forecast the technical advances that will be needed to continue driving the development of membrane protein therapeutics.

摘要

膜蛋白具有极大的研究价值,尤其是因为它们富含治疗应用的靶点。在临床前和临床研究中,已经对各种膜蛋白作为治疗制剂(如药物或抗体)靶点的适用性进行了研究。然而,对于治疗应用而言,蛋白质必须尽可能以接近其天然构象的形式表达和纯化。对于膜蛋白来说,这已被证明是困难的,因为它们的天然构象需要与合适的细胞膜结合。解决这个问题的一种方法是使用细胞外囊泡作为展示平台。外泌体和微囊泡是从大多数细胞中释放出来的膜性细胞外囊泡。它们的膜可能为膜蛋白呈现其正确的构象、活性和膜分布提供有利的微环境;此外,膜蛋白在生物发生后可在细胞外囊泡表面聚集成微结构域。在这篇综述中,我们概述了基于细胞外囊泡(外泌体和小尺寸微囊泡)的治疗方法的最新进展,评估了目前对这些制剂的生物学理解,并预测了推动膜蛋白治疗发展所需的技术进步。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/faec/5844050/cb1396129f17/ZJEV_A_1440131_F0001_C.jpg

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