Abedinzadeh Maria, Gaeini Mahdieh, Sardari Soroush
Drug Design and Bioinformatics Unit, Medical Biotechnology Department, Biotechnology Research Centre, Pasteur Institute of Iran, Tehran, Iran.
Drug Design and Bioinformatics Unit, Medical Biotechnology Department, Biotechnology Research Centre, Pasteur Institute of Iran, Tehran, Iran
J Antimicrob Chemother. 2015 May;70(5):1285-9. doi: 10.1093/jac/dku570. Epub 2015 Feb 12.
TB, caused by Mycobacterium tuberculosis, is one the leading infectious diseases worldwide. There is an urgent need to discover new drugs with unique structures and uncommon mechanisms of action to treat M. tuberculosis and combat antimycobacterial resistance. Naturally occurring compounds contain a wide diversity of chemical structures, displaying a wide range of in vitro potency towards M. tuberculosis. A number of recent studies have shown that natural antimycobacterial peptides can disrupt the function of the mycobacterial cell wall through different modes of action and thereafter interact with intracellular targets, including nucleic acids, enzymes and even organelles. More importantly, the probability of antimycobacterial resistance is low. This review presents several natural antimicrobial peptides isolated from different organism sources, including bacteria, fungi, plants and animals. In addition, the molecular features of these molecules are the subject of much attention. Such peptides have common traits among their chemical features, which may be correlated with their biological activities; hence, different parts of the molecular structures can be modified in order to increase penetration into the target cells. This review also summarizes the available information on the properties of antimycobacterial peptides associated with their biological activities.
由结核分枝杆菌引起的结核病是全球主要的传染病之一。迫切需要发现具有独特结构和罕见作用机制的新药,以治疗结核分枝杆菌并对抗抗分枝杆菌耐药性。天然存在的化合物含有多种多样的化学结构,对结核分枝杆菌显示出广泛的体外效力。最近的一些研究表明,天然抗分枝杆菌肽可以通过不同的作用方式破坏分枝杆菌细胞壁的功能,进而与细胞内靶点相互作用,包括核酸、酶甚至细胞器。更重要的是,产生抗分枝杆菌耐药性的可能性较低。本综述介绍了几种从不同生物体来源分离得到的天然抗菌肽,包括细菌、真菌、植物和动物。此外,这些分子的分子特征备受关注。此类肽在其化学特征上具有共同特点,这可能与其生物学活性相关;因此,可以对分子结构的不同部分进行修饰,以增加对靶细胞的穿透能力。本综述还总结了与抗分枝杆菌肽生物学活性相关的现有信息。