Jiangsu Key Laboratory of Druggability of Biopharmaceuticals and State Key Laboratory of Natural Medicines, School of Life Science and Technology, China Pharmaceutical University, Nanjing 210009, China.
Jiangsu Key Laboratory of Neurodegeneration, Nanjing Medical University, Nanjing 210009, China.
Acta Biomater. 2023 Jul 1;164:74-93. doi: 10.1016/j.actbio.2023.04.019. Epub 2023 Apr 17.
Although polyethylene glycol (PEG), or "PEGylation" has become a widely applied approach for improving the efficiency of drug delivery, the immunogenicity and non-biodegradability of this synthetic polymer have prompted an evident need for alternatives. To overcome these caveats and to mimic PEG -or other natural or synthetic polymers- for the purpose of drug half-life extension, unstructured polypeptides are designed. Due to their tunable length, biodegradability, low immunogenicity and easy production, unstructured polypeptides have the potential to replace PEG as the preferred technology for therapeutic protein/peptide delivery. This review provides an overview of the evolution of unstructured polypeptides, starting from natural polypeptides to engineered polypeptides and discusses their characteristics. Then, it is described that unstructured polypeptides have been successfully applied to numerous drugs, including peptides, proteins, antibody fragments, and nanocarriers, for half-life extension. Innovative applications of unstructured peptides as releasable masks, multimolecular adaptors and intracellular delivery carriers are also discussed. Finally, challenges and future perspectives of this promising field are briefly presented. STATEMENT OF SIGNIFICANCE: Polypeptide fusion technology simulating PEGylation has become an important topic for the development of long-circulating peptide or protein drugs without reduced activity, complex processes, and kidney injury caused by PEG modification. Here we provide a detailed and in-depth review of the recent advances in unstructured polypeptides. In addition to the application of enhanced pharmacokinetic performance, emphasis is placed on polypeptides as scaffolders for the delivery of multiple drugs, and on the preparation of reasonably designed polypeptides to manipulate the performance of proteins and peptides. This review will provide insight into future application of polypeptides in peptide or protein drug development and the design of novel functional polypeptides.
尽管聚乙二醇(PEG)或“PEGylation”已成为提高药物递送效率的广泛应用方法,但这种合成聚合物的免疫原性和不可生物降解性促使人们明显需要替代品。为了克服这些缺点,并模仿 PEG 或其他天然或合成聚合物,用于延长药物半衰期,设计了无规多肽。由于其可调节的长度、生物降解性、低免疫原性和易于生产,无规多肽有可能取代 PEG 作为治疗性蛋白/肽递送的首选技术。
本文综述了无规多肽的发展历程,从天然多肽到工程多肽,并讨论了它们的特性。然后,描述了无规多肽已成功应用于许多药物,包括肽、蛋白质、抗体片段和纳米载体,以延长半衰期。还讨论了无规多肽作为可释放掩模、多分子接头和细胞内递药载体的创新应用。最后,简要介绍了该有前途领域的挑战和未来展望。
模拟 PEGylation 的多肽融合技术已成为开发无活性、复杂工艺和 PEG 修饰引起肾损伤的长效肽或蛋白药物的重要课题。
在这里,我们提供了无规多肽最新进展的详细和深入的综述。除了增强药代动力学性能的应用外,重点还放在多肽作为多种药物递药的支架上,以及合理设计多肽来操纵蛋白质和肽的性能上。
这篇综述将为多肽在肽或蛋白药物开发和新型功能多肽设计中的未来应用提供思路。