Moreno-Vargas Liliana Marisol, Prada-Gracia Diego
Research Unit on Computational Biology and Drug Design, Children's Hospital of Mexico Federico Gómez, Mexico City 06720, Mexico.
Int J Mol Sci. 2024 Dec 25;26(1):59. doi: 10.3390/ijms26010059.
Cell-penetrating peptides (CPPs) are a diverse group of peptides, typically composed of 4 to 40 amino acids, known for their unique ability to transport a wide range of substances-such as small molecules, plasmid DNA, small interfering RNA, proteins, viruses, and nanoparticles-across cellular membranes while preserving the integrity of the cargo. CPPs exhibit passive and non-selective behavior, often requiring functionalization or chemical modification to enhance their specificity and efficacy. The precise mechanisms governing the cellular uptake of CPPs remain ambiguous; however, electrostatic interactions between positively charged amino acids and negatively charged glycosaminoglycans on the membrane, particularly heparan sulfate proteoglycans, are considered the initial crucial step for CPP uptake. Clinical trials have highlighted the potential of CPPs in diagnosing and treating various diseases, including cancer, central nervous system disorders, eye disorders, and diabetes. This review provides a comprehensive overview of CPP classifications, potential applications, transduction mechanisms, and the most relevant algorithms to improve the accuracy and reliability of predictions in CPP development.
细胞穿透肽(CPPs)是一类多样的肽,通常由4至40个氨基酸组成,以其独特的能力而闻名,即能够在保持货物完整性的同时,将多种物质——如小分子、质粒DNA、小干扰RNA、蛋白质、病毒和纳米颗粒——转运穿过细胞膜。CPPs表现出被动和非选择性行为,通常需要功能化或化学修饰以提高其特异性和功效。控制CPPs细胞摄取的精确机制仍不明确;然而,带正电荷的氨基酸与膜上带负电荷的糖胺聚糖(特别是硫酸乙酰肝素蛋白聚糖)之间的静电相互作用被认为是CPP摄取的初始关键步骤。临床试验突出了CPPs在诊断和治疗各种疾病(包括癌症、中枢神经系统疾病、眼部疾病和糖尿病)方面的潜力。本综述全面概述了CPP的分类、潜在应用、转导机制以及在CPP开发中提高预测准确性和可靠性的最相关算法。