Institute of Technology, University of Tartu, Tartu, Estonia.
Department Biochemistry and Biophysics, Stockholm University, Stockholm, Sweden.
Expert Opin Drug Discov. 2021 May;16(5):553-565. doi: 10.1080/17460441.2021.1851187. Epub 2020 Dec 1.
: The capability of cell-penetrating peptides (CPP), also known as protein transduction domains (PTD), to enter into cells possibly with an attached cargo, makes their application as delivery vectors or as direct therapeutics compelling. They are generally biocompatible, nontoxic, and easy to synthesize and modify. Three decades after the discovery of the first CPPs, ~2,000 CPP sequences have been identified, and many more predicted. Nevertheless, the field has a strong commitment to authenticate new, more efficient, and specific CPPs.: Although a scattering of CPPs have been found by chance, various systematic approaches have been developed and refined over the years to directly aid the identification and depiction of new peptide-based delivery vectors or therapeutics. Here, the authors give an overview of CPPs, and review various approaches of discovering new ones. An emphasis is placed on methods, as these have advanced rapidly in recent years.: Although there are many known CPPs, there is a need to find more efficient and specific CPPs. Several approaches are used to identify such sequences. The success of these approaches depends on the advancement of others and the successful prediction of CPP sequences relies on experimental data.
: 细胞穿透肽(CPP),也称为蛋白转导结构域(PTD),具有携带 cargo 进入细胞的能力,这使得它们作为递送载体或直接治疗剂的应用具有吸引力。它们通常具有生物相容性、低毒性、易于合成和修饰。在发现第一批 CPP 三十年后,已经鉴定出约 2000 种 CPP 序列,并且预测了更多的 CPP 序列。尽管如此,该领域仍致力于验证新的、更有效和更特异的 CPP。: 虽然偶然发现了一些 CPP,但多年来已经开发和完善了各种系统方法,以直接帮助鉴定和描述新的基于肽的递药载体或治疗剂。在这里,作者概述了 CPP,并回顾了发现新 CPP 的各种方法。重点介绍了方法,因为这些方法近年来发展迅速。: 虽然有许多已知的 CPP,但仍需要找到更有效和特异的 CPP。已经使用了几种方法来鉴定这些序列。这些方法的成功取决于其他方法的进步,并且 CPP 序列的成功预测依赖于实验数据。