Unlocking the Potential of Retro-Inverso (RI) Peptides as Future Drug Candidates

IF 2 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY International Journal of Peptide Research and Therapeutics Pub Date : 2024-09-10 DOI:10.1007/s10989-024-10639-1
Othman Al Musaimi
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Abstract

Background

With the rising demand for peptide-based drugs, enhancing their stability against proteolytic degradation has become a critical challenge. Strategies to improve peptide stability include cyclization, substitution of L-amino acids with D-amino acids, incorporation of β-amino acids, and various formulation techniques. An innovative approach involves modifying the peptide backbone by reversing the amide bond direction and inverting the stereochemistry of amino acids in the same segment. This approach results in the formation of retro-inverso peptides, which offer increased stability, permeability, and cellular uptake.

Purpose

The aim of this review is to provide a comprehensive analysis of retro-inverso peptides, focusing on their concept, synthesis, and applications as potential therapeutic agents, drug delivery systems, and in aesthetic applications.

Methods

The review explores the theoretical underpinnings of retro-inverso peptide design and its application to both linear and cyclic peptides. The synthesis strategies of retro-inverso peptides are discussed in detail, along with their formulation and practical utility in various biomedical fields.

Results

Retro-inverso peptides show promise in enhancing peptide stability and improving biological properties such as permeability and cellular uptake. Their unique structure offers advantages in drug development and potential as therapeutic agents or drug carriers.

Conclusion

Retro-inverso peptides represent a valuable strategy for overcoming the limitations of conventional peptides, especially regarding stability and bioavailability. This review highlights their potential in therapeutic development and other applications, reinforcing the importance of continued research and innovation in peptide chemistry.

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挖掘逆转录病毒 (RI) 多肽作为未来候选药物的潜力
背景随着多肽类药物需求的不断增加,提高其抗蛋白水解降解的稳定性已成为一项严峻的挑战。提高多肽稳定性的策略包括环化、用 D-氨基酸取代 L-氨基酸、加入 β-氨基酸以及各种制剂技术。一种创新方法是通过逆转酰胺键方向和颠倒同一区段氨基酸的立体化学来改变肽骨。本综述旨在全面分析反转肽,重点关注其概念、合成以及作为潜在治疗剂、给药系统和美容应用的应用。方法本综述探讨了反转肽设计的理论基础及其在线性肽和环状肽中的应用。结果反转录肽在提高肽的稳定性、改善生物特性(如渗透性和细胞吸收)方面显示出前景。它们的独特结构为药物开发提供了优势,并具有作为治疗剂或药物载体的潜力。结论反式肽是克服传统肽局限性的重要策略,尤其是在稳定性和生物利用度方面。本综述强调了它们在治疗开发和其他应用方面的潜力,并强调了继续研究和创新多肽化学的重要性。
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来源期刊
CiteScore
5.50
自引率
8.00%
发文量
131
审稿时长
>12 weeks
期刊介绍: The International Journal for Peptide Research & Therapeutics is an international, peer-reviewed journal focusing on issues, research, and integration of knowledge on the latest developments in peptide therapeutics. The Journal brings together in a single source the most exciting work in peptide research, including isolation, structural characterization, synthesis and biological activity of peptides, and thereby aids in the development of unifying concepts from diverse perspectives. The Journal invites substantial contributions in the following thematic areas: -New advances in peptide drug delivery systems. -Application of peptide therapeutics to specific diseases. -New advances in synthetic methods. -The development of new procedures for construction of peptide libraries and methodology for screening of such mixtures. -The use of peptides in the study of enzyme specificity and mechanism, receptor binding and antibody/antigen interactions -Applications of such techniques as chromatography, electrophoresis, NMR and X-ray crystallography, mass spectrometry.
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