Cell-free protein synthesis and vesicle systems for programmable therapeutic manufacturing and delivery.

IF 6.5 3区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Wonhee Kim, Jinjoo Han, Shraddha Chauhan, Jeong Wook Lee
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Abstract

The convergence of cell-free protein synthesis (CFPS) and vesicle-based delivery platforms presents a promising avenue for therapeutic development. The open environment of CFPS offers precise control over protein synthesis by enabling the modulation of synthetic conditions. Additionally, vesicle-based platforms provide enhanced stability, bioavailability, and targeted delivery. This synergy facilitates the efficient production of complex proteins-including membrane proteins, antibody fragments, and proteins requiring post-translational modifications (PTMs)-and supports novel drug delivery strategies. While existing reviews have covered synthetic cells and biomanufacturing broadly, a dedicated analysis of CFPS system-containing vesicles (CFVs) for therapeutic applications remains absent from the literature. This review addresses this knowledge gap by providing a comprehensive examination of CFVs, highlighting their potential as programmable drug delivery platforms through the integration of genetic circuits. It emphasizes the advantages of CFPS over traditional cell-based approaches and explores the synergistic benefits of combining CFPS with various vesicle systems. These systems offer dynamic control over therapeutic protein production and targeted delivery, enabling precise responses to specific signals in complex environments. Although challenges such as low protein yield and imperfect targeting remain, potential optimization strategies are discussed. This analysis highlights the significant potential of integrating CFPS and vesicle-based delivery to advance biomanufacturing, therapeutic development, and synthetic cell systems, thereby opening new avenues in medicine and healthcare.

无细胞蛋白合成和囊泡系统用于可编程治疗制造和递送。
无细胞蛋白合成(CFPS)和基于囊泡的递送平台的融合为治疗发展提供了一条有前途的途径。CFPS的开放环境通过调节合成条件提供了对蛋白质合成的精确控制。此外,基于囊泡的平台提供了更高的稳定性、生物利用度和靶向递送。这种协同作用促进了复杂蛋白的高效生产,包括膜蛋白、抗体片段和需要翻译后修饰(PTMs)的蛋白,并支持新的药物递送策略。虽然现有的综述已经广泛地涵盖了合成细胞和生物制造,但文献中仍然缺乏对CFPS系统含囊泡(CFVs)治疗应用的专门分析。这篇综述通过对cfv的全面研究来解决这一知识缺口,强调了它们通过整合遗传电路作为可编程药物输送平台的潜力。它强调了CFPS相对于传统的基于细胞的方法的优势,并探讨了将CFPS与各种囊泡系统结合的协同效益。这些系统可以动态控制治疗蛋白的产生和靶向递送,从而在复杂环境中对特定信号做出精确反应。尽管存在低蛋白产量和不完善的靶向性等挑战,但仍讨论了潜在的优化策略。该分析强调了整合CFPS和基于囊泡的递送的巨大潜力,以推进生物制造,治疗开发和合成细胞系统,从而开辟了医学和医疗保健的新途径。
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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来源期刊
Journal of Biological Engineering
Journal of Biological Engineering BIOCHEMICAL RESEARCH METHODS-BIOTECHNOLOGY & APPLIED MICROBIOLOGY
CiteScore
7.10
自引率
1.80%
发文量
32
审稿时长
17 weeks
期刊介绍: Biological engineering is an emerging discipline that encompasses engineering theory and practice connected to and derived from the science of biology, just as mechanical engineering and electrical engineering are rooted in physics and chemical engineering in chemistry. Topical areas include, but are not limited to: Synthetic biology and cellular design Biomolecular, cellular and tissue engineering Bioproduction and metabolic engineering Biosensors Ecological and environmental engineering Biological engineering education and the biodesign process As the official journal of the Institute of Biological Engineering, Journal of Biological Engineering provides a home for the continuum from biological information science, molecules and cells, product formation, wastes and remediation, and educational advances in curriculum content and pedagogy at the undergraduate and graduate-levels. Manuscripts should explore commonalities with other fields of application by providing some discussion of the broader context of the work and how it connects to other areas within the field.
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