Engineered Bacteriophages: Advances in Phage Genome Redesign Strategies for Therapeutic and Environmental Applications.

IF 1 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Marzieh Rezaei, Amir Jalali, Dheyaa Hussein Sadah Al-Azzawi
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引用次数: 0

Abstract

Bacteriophages, or phages, have emerged as powerful platforms in synthetic biology, offering innovative solutions for therapeutic and environmental challenges through advanced genome redesign strategies. This review explores a wide range of phage engineering techniques, including CRISPR (clustered regularly-interspaced short palindromic repeats)-Cas systems, phage display, random and site-directed mutagenesis, retrons, and rebooting approaches, highlighting their potential to create phages with tailored functionalities. CRISPR-Cas systems enable precise genome editing, allowing the development of phages with expanded host ranges, biofilm degradation capabilities, and targeted antimicrobial activity. Phage display facilitates the presentation of peptides on phage surfaces, enabling applications in targeted drug delivery, tumor imaging, and bioremediation. Beyond these, techniques like retron-mediated recombination and homologous recombination offer additional avenues for precise phage genome modification. In the therapeutic realm, engineered phages show promise in combating drug-resistant infections, modulating the microbiome, and delivering targeted therapies for cancer and other diseases. Environmentally, phage-based strategies, such as the use of phage-displayed metal-binding peptides, provide innovative solutions for bioremediation and reducing exposure to toxic heavy metals. This review also addresses challenges, such as phage resistance, immune responses, and the limitations of current engineering methods, while exploring future directions, including the development of improved CRISPR systems, phage-based biosensors, and high-throughput screening platforms. By integrating cutting-edge genome redesign strategies with diverse applications, this review underscores the transformative potential of engineered bacteriophages in addressing global healthcare and environmental sustainability challenges.

工程噬菌体:用于治疗和环境应用的噬菌体基因组重新设计策略的进展。
噬菌体已经成为合成生物学中强大的平台,通过先进的基因组重新设计策略为治疗和环境挑战提供创新的解决方案。这篇综述探讨了广泛的噬菌体工程技术,包括CRISPR(聚集规则间隔短回文重复序列)-Cas系统,噬菌体展示,随机和定点突变,逆转录和重新启动方法,强调了它们创造具有定制功能的噬菌体的潜力。CRISPR-Cas系统能够实现精确的基因组编辑,允许噬菌体的发展具有扩展的宿主范围,生物膜降解能力和靶向抗菌活性。噬菌体展示促进了肽在噬菌体表面的呈现,使其在靶向药物递送、肿瘤成像和生物修复方面的应用成为可能。除此之外,逆转录介导重组和同源重组等技术为精确修饰噬菌体基因组提供了额外的途径。在治疗领域,工程噬菌体在对抗耐药感染、调节微生物群以及提供针对癌症和其他疾病的靶向治疗方面显示出前景。在环境方面,基于噬菌体的策略,如使用噬菌体显示的金属结合肽,为生物修复和减少有毒重金属暴露提供了创新的解决方案。这篇综述还讨论了挑战,如噬菌体耐药性、免疫反应和当前工程方法的局限性,同时探索了未来的方向,包括改进CRISPR系统、基于噬菌体的生物传感器和高通量筛选平台的发展。通过整合尖端的基因组重新设计策略和多种应用,本综述强调了工程噬菌体在解决全球医疗保健和环境可持续性挑战方面的变革潜力。
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
Protein and Peptide Letters
Protein and Peptide Letters 生物-生化与分子生物学
CiteScore
2.90
自引率
0.00%
发文量
98
审稿时长
2 months
期刊介绍: Protein & Peptide Letters publishes letters, original research papers, mini-reviews and guest edited issues in all important aspects of protein and peptide research, including structural studies, advances in recombinant expression, function, synthesis, enzymology, immunology, molecular modeling, and drug design. Manuscripts must have a significant element of novelty, timeliness and urgency that merit rapid publication. Reports of crystallization and preliminary structure determination of biologically important proteins are considered only if they include significant new approaches or deal with proteins of immediate importance, and preliminary structure determinations of biologically important proteins. Purely theoretical/review papers should provide new insight into the principles of protein/peptide structure and function. Manuscripts describing computational work should include some experimental data to provide confirmation of the results of calculations. Protein & Peptide Letters focuses on: Structure Studies Advances in Recombinant Expression Drug Design Chemical Synthesis Function Pharmacology Enzymology Conformational Analysis Immunology Biotechnology Protein Engineering Protein Folding Sequencing Molecular Recognition Purification and Analysis
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