摘要
肽和蛋白质控制和指导细胞功能和通讯的各个方面。经过大自然磨练了数百万年,它们也表现出无与伦比的特异性。或它们的生物靶点。这是继续关注肽作为有希望的候选药物的基础。然而,由于缺乏化学物质,阻碍了肽类药物在活性药物中的发展。ND药动学稳定性与大规模生产成本。克服这些障碍的方法之一是开发出能够保留的重要结构特征的聚合物体系这些生物活性肽,而便宜、容易生产和利用化学。 这篇综述用了模仿抗菌宿主防御肽的聚合物的例子说明了这些原理。宿主防御肽已被确定为一些最重要的。导致下一代抗生素,因为他们通常表现出广谱抗菌能力,对人体细胞的毒性低,对目前已知的机制很少的敏感性。细菌的耐药性。然而,由于这些肽作为药物的局限性,他们从板凳到诊所的运动尚未实现。文献提供了许多聚合物的例子。那已经能够模仿这些肽通过各级结构,从特定的氨基酸侧链,通过更多的全局特征,如整体电荷,分子量D立体结构(如α螺旋)。所得到的优化聚合物能够保留肽的活性剖面,但在合成大分子结构中可能更好。适合新一代抗菌疗法的发展。这项工作不仅产生了新的重要线索,以对抗日益严重的抗生素耐药性威胁,而且可能也会产生耐药性。聚合物模仿其他重要生物活性肽的新途径。
关键词: 抗菌肽,聚合物,细菌,肽模拟,宿主防御肽。
Current Medicinal Chemistry
Title:Antimicrobial Polymers: Mimicking Amino Acid Functionali ty, Sequence Control and Three-dimensional Structure of Host-defen se Peptides
Volume: 24 Issue: 19
关键词: 抗菌肽,聚合物,细菌,肽模拟,宿主防御肽。
摘要: Peptides and proteins control and direct all aspects of cellular function and communication. Having been honed by nature for millions of years, they also typically display an unsurpassed specificity for their biological targets. This underlies the continued focus on peptides as promising drug candidates. However, the development of peptides into viable drugs is hampered by their lack of chemical and pharmacokinetic stability and the cost of large scale production. One method to overcome such hindrances is to develop polymer systems that are able to retain the important structural features of these biologically active peptides, while being cheaper and easier to produce and manipulate chemically.
This review illustrates these principles using examples of polymers designed to mimic antimicrobial host-defence peptides. The host-defence peptides have been identified as some of the most important leads for the next generation of antibiotics as they typically exhibit broad spectrum antimicrobial ability, low toxicity toward human cells and little susceptibility to currently known mechanisms of bacterial resistance. Their movement from the bench to clinic is yet to be realised, however, due to the limitations of these peptides as drugs. The literature provides a number of examples of polymers that have been able to mimic these peptides through all levels of structure, starting from specific amino acid sidechains, through to more global features such as overall charge, molecular weight and threedimensional structure (e.g. α-helical). The resulting optimised polymers are able retain the activity profile of the peptides, but within a synthetic macromolecular construct that may be better suited to the development of a new generation of antimicrobial therapeutics. Such work has not only produced important new leads to combat the growing threat of antibiotic resistance, but may also open up new ways for polymers to mimic other important classes of biologically active peptides.Export Options
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Cite this article as:
Antimicrobial Polymers: Mimicking Amino Acid Functionali ty, Sequence Control and Three-dimensional Structure of Host-defen se Peptides, Current Medicinal Chemistry 2017; 24 (19) . https://dx.doi.org/10.2174/0929867324666170116122322
DOI https://dx.doi.org/10.2174/0929867324666170116122322 |
Print ISSN 0929-8673 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-533X |
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