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新一代细胞穿透肽:功能及潜在临床应用

New generation of cell-penetrating peptides: Functionality and potential clinical application.

作者信息

Reissmann Siegmund, Filatova Margarita P

机构信息

Faculty of Biological Sciences, Institute of Biochemistry and Biophysics, Friedrich Schiller University, Dornburger Str. 25, Jena, Thueringia, 07743, Germany.

Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, Moscow, Russia.

出版信息

J Pept Sci. 2021 May;27(5):e3300. doi: 10.1002/psc.3300. Epub 2021 Feb 21.

Abstract

Cell-penetrating peptides (CPPs) can transport various cargoes through membranes of live cells. Since the first generations of CPPs suffered from insufficient cell and tissue selectivity, stability against proteases, and escape from endosomes, a new generation of peptides, with optimized properties, was developed. These are either derived from natural sources or created through the combination of multivalent structures. The second method allows achieving high internalization efficiency, high cell and tissue selectivity, and release from endosomes via hybrid structures, combining sequences for endosomal release, homing sequences, and sequences for activation at the target tissue and for local delivery of cargoes. CPPs with innate tumor selectivity include azurin, crotamine, maurocalcine, lycosin-I, buffalo cathelicidin, and peptide CB5005. Some of them can penetrate the membranes of live cells and influence intracellular signaling pathways, thereby exerting cytotoxic effects against tumor cells. To obtain multilayer penetration and stabilization against proteolytic degradation, as well as for better handling, CPPs are often conjugated to nanoparticles. A special problem for tumor treatment is the efficiency of drug transport through three-dimensional cell cultures. Therefore, the capability of CPPs to deliver the drug even to the innermost tissues is of crucial importance. Notably, the ability of certain CPPs to penetrate barriers such as skin, the blood-brain barrier (BBB), and cornea or conjunctiva of eyes enabled the replacement of dangerous and painful injections with soothing sprays, creams, and drops. However, it is difficult to rank the efficacy of CPPs because transport efficiency and tissue selectivity depend not only on the CPP itself but also on the target tissue or organ, as well as on the cargo and method of CPP-cargo coupling. Therefore, the present review describes some examples of new-generation CPPs and aims to provide advice on how to find or create the right CPP for a given task.

摘要

细胞穿透肽(CPPs)能够携带各种物质穿过活细胞的膜。由于第一代细胞穿透肽在细胞和组织选择性、抗蛋白酶稳定性以及从内涵体逃逸等方面存在不足,因此开发了具有优化特性的新一代肽。这些肽要么来源于天然来源,要么通过多价结构的组合产生。第二种方法能够通过混合结构实现高内化效率、高细胞和组织选择性以及从内涵体释放,该混合结构结合了内涵体释放序列、归巢序列以及在靶组织激活和物质局部递送的序列。具有天然肿瘤选择性的细胞穿透肽包括天青蛋白、巴曲酶、芋螺毒素、狼蛛毒素-I、水牛防御素以及肽CB5005。其中一些能够穿透活细胞的膜并影响细胞内信号通路,从而对肿瘤细胞发挥细胞毒性作用。为了实现多层穿透和抗蛋白水解降解的稳定性,以及为了更便于操作,细胞穿透肽通常与纳米颗粒偶联。肿瘤治疗中的一个特殊问题是药物通过三维细胞培养物的运输效率。因此,细胞穿透肽将药物递送至最内层组织的能力至关重要。值得注意的是,某些细胞穿透肽穿透皮肤、血脑屏障(BBB)以及眼睛的角膜或结膜等屏障的能力,使得可以用舒缓的喷雾剂、乳膏和滴剂取代危险且痛苦的注射。然而,很难对细胞穿透肽的功效进行排名,因为运输效率和组织选择性不仅取决于细胞穿透肽本身,还取决于靶组织或器官,以及货物和细胞穿透肽 - 货物偶联的方法。因此,本综述描述了一些新一代细胞穿透肽的实例,并旨在就如何为给定任务找到或创建合适的细胞穿透肽提供建议。

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