三联体 Holin、Endolysin 和 Spanin 的分子机制:噬菌体诱导的细胞裂解及其治疗应用的关键角色。

IF 1 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Protein and Peptide Letters Pub Date : 2024-01-01 DOI:10.2174/0109298665181166231212051621
Safia Samir
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引用次数: 0

摘要

近年来,噬菌体疗法作为治疗多重耐药性(MDR)感染的一种可能替代疗法备受关注。溶解性噬菌体编码用于破坏细菌宿主包膜的蛋白质。噬菌体产生内溶素壁层酶,它们是噬菌体编码的肽聚糖水解酶(PGHs),可在噬菌体溶解繁殖周期结束时酶解宿主细菌的肽聚糖(PG)或金霉素层。噬菌体全蛋白调节内溶菌素进入肽聚糖的途径,在特定的 "溶解时钟 "时刻启动溶解过程。噬菌体spanins会破坏外膜。Holin/Endolysin/Spanin 可用作新型抗菌剂,以对抗细菌引起的感染。这些蛋白质正引起各行各业的兴趣,包括制药、食品、生物技术和医学等领域。在这篇综述中,我们强调了这些蛋白质的重要性及其在动物研究中的应用。此外,还提到了一些临床试验。
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Molecular Machinery of the Triad Holin, Endolysin, and Spanin: Key Players Orchestrating Bacteriophage-Induced Cell Lysis and their Therapeutic Applications.

Phage therapy, a promising alternative to combat multidrug-resistant bacterial infections, harnesses the lytic cycle of bacteriophages to target and eliminate bacteria. Key players in this process are the phage lysis proteins, including holin, endolysin, and spanin, which work synergistically to disrupt the bacterial cell wall and induce lysis. Understanding the structure and function of these proteins is crucial for the development of effective therapies. Recombinant versions of these proteins have been engineered to enhance their stability and efficacy. Recent progress in the field has led to the approval of bacteriophage-based therapeutics as drugs, paving the way for their clinical use. These proteins can be combined in phage cocktails or combined with antibiotics to enhance their activity against bacterial biofilms, a common cause of treatment failure. Animal studies and clinical trials are being conducted to evaluate the safety and efficacy of phage therapy in humans. Overall, phage therapy holds great potential as a valuable tool in the fight against multidrug- resistant bacteria, offering hope for the future of infectious disease treatment.

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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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