赖氨酸
溶解循环
肽聚糖
噬菌体
生物
溶解
微生物学
细菌细胞结构
噬菌体疗法
单元格信封
细菌
细胞生物学
病毒学
生物化学
大肠杆菌
病毒
遗传学
基因
出处
期刊:Protein and Peptide Letters
[Bentham Science]
日期:2024-01-23
卷期号:31 (2): 85-96
被引量:1
标识
DOI:10.2174/0109298665181166231212051621
摘要
Abstract: 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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