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Membrane-Active Peptides from Marine Organisms-Antimicrobials, Cell-Penetrating Peptides and Peptide Toxins: Applications and Prospects

机译:膜生物活性肽从海洋生物-抗菌素,细胞穿透肽和肽毒素:应用和前景。

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摘要

Marine organisms are known to be a rich and unique source of bioactive compounds as they are exposed to extreme conditions in the oceans. The present study is an attempt to briefly describe some of the important membrane-active peptides (MAPs) such as antimicrobial peptides (AMPs), cell-penetrating peptides (CPPs) and peptide toxins from marine organisms. Since both AMPs and CPPs play a role in membrane perturbation and exhibit interchangeable role, they can speculatively fall under the broad umbrella of MAPs. The study focuses on the structural and functional characteristics of different classes of marine MAPs. Further, AMPs are considered as a potential remedy to antibiotic resistance acquired by several pathogens. Peptides from marine organisms show novel post-translational modifications such as cysteine knots, halogenation and histidino-alanine bridge that enable these peptides to withstand harsh marine environmental conditions. These unusual modifications of AMPs from marine organisms are expected to increase their half-life in living systems, contributing to their increased bioavailability and stability when administered as drug in in vivo systems. Apart from AMPs, marine toxins with membrane-perturbing properties could be essentially investigated for their cytotoxic effect on various pathogens and their cell-penetrating activity across various mammalian cells. The current review will help in identifying the MAPs from marine organisms with crucial post-translational modifications that can be used as template for designing novel therapeutic agents and drug-delivery vehicles for treatment of human diseases.
机译:由于海洋生物暴露于海洋的极端条件下,因此是丰富而独特的生物活性化合物的来源。本研究试图简要描述一些重要的膜活性肽(MAPs),例如抗微生物肽(AMPs),穿透细胞的肽(CPPs)和来自海洋生物的肽毒素。由于AMP和CPP都在膜扰动中发挥作用,并且表现出可互换的作用,因此它们可以推测地属于MAP的保护范围。该研究侧重于不同类别的海洋MAP的结构和功能特征。此外,AMP被认为是对几种病原体获得的抗生素耐药性的潜在疗法。来自海洋生物的肽显示出新的翻译后修饰,例如半胱氨酸结,卤化和组氨酸-丙氨酸桥,使这些肽能够承受恶劣的海洋环境条件。这些来自海洋生物的AMPs的非常规修饰有望延长其在生命系统中的半衰期,从而有助于在体内系统中作为药物给药时提高其生物利用度和稳定性。除了AMPs外,具有膜扰动特性的海洋毒素对各种病原体的细胞毒性作用及其在各种哺乳动物细胞中的细胞穿透活性都可以进行实质性研究。目前的审查将有助于从具有重要翻译后修饰的海洋生物中识别出MAP,这些MAP可以用作设计用于治疗人类疾病的新型治疗剂和药物递送载体的模板。

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