Ribozyme biotechnology: emerging opportunities for medical applications in the RNA therapeutics era.

Medical review (Berlin, Germany) Pub Date : 2025-12-16 eCollection Date: 2026-02-01 DOI:10.1515/mr-2025-0062
Jingjing Zhang, Zhiqin Xi, Ming Zhao, Jie Bai, Zhenzhen Li, Xuelin Zhan, Ying Zhang, Yijin Liu
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Abstract

RNA-based medicines have transformed modern therapeutics, exemplified by the clinical success of small interfering RNAs (siRNAs), antisense oligonucleotides (ASOs), and mRNA vaccines. Small self-cleaving ribozymes - compact catalytic RNA species capable of programmable cleavage and ligation - were among the earliest RNA drugs explored, yet their progress was initially hindered by instability, nuclease degradation, inefficient intracellular delivery, and immune activation. In this Perspective, we discuss how recent technological convergence has revived their potential. Comparative genomics has uncovered new catalytic classes, including Twister, Pistol, Hatchet, and Hovlinc ribozymes, thereby expanding the catalytic repertoire. High-resolution structural and computational studies have elucidated their reaction architectures, while chemical modifications and advanced nanocarrier systems - such as DNA nanostructures, spherical nucleic acids, and lipid nanoparticles - have markedly improved molecular stability and delivery efficiency. Emerging applications, from ligand-responsive aptazymes and ribozyme-SNA conjugates to the StitchR RNA trans-ligation platform, further illustrate the expanding biomedical versatility of catalytic RNA. Together, these advances are redefining the role of ribozymes in oncology, virology, and genetic medicine. No longer a dormant concept, ribozymes now stand as an evolving frontier - rationally engineered catalysts that continue to inspire technological creativity and renewed optimism in RNA therapeutics.

Abstract Image

核酶生物技术:RNA治疗时代医学应用的新机遇。
基于rna的药物已经改变了现代治疗方法,例如小干扰rna (sirna)、反义寡核苷酸(ASOs)和mRNA疫苗的临床成功。小型自切割核糖酶是一种紧凑的催化RNA,能够进行可编程的切割和连接,是最早被探索的RNA药物之一,但它们的进展最初受到不稳定性、核酸酶降解、细胞内递送效率低下和免疫激活的阻碍。在这个视角中,我们讨论了最近的技术融合如何恢复了它们的潜力。比较基因组学已经发现了新的催化类,包括Twister、Pistol、Hatchet和Hovlinc核酶,从而扩大了催化库。高分辨率结构和计算研究已经阐明了它们的反应结构,而化学修饰和先进的纳米载体系统——如DNA纳米结构、球形核酸和脂质纳米颗粒——显著提高了分子稳定性和递送效率。从配体反应性适配酶和核酶- sna偶联物到StitchR RNA反式连接平台等新兴应用,进一步说明了催化RNA在生物医学上的多功能性。总之,这些进展正在重新定义核酶在肿瘤学、病毒学和遗传医学中的作用。核糖酶不再是一个处于休眠状态的概念,它现在站在一个不断发展的前沿——理性设计的催化剂,继续激发技术创造力,并在RNA治疗中重新获得乐观。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
1.30
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