首页> 外文OA文献 >Design, Synthesis, and Evaluation of Amphiphilic Cyclic and Linear Peptides Composed of Hydrophobic and Positively-Charged Amino Acids as Antibacterial Agents
【2h】

Design, Synthesis, and Evaluation of Amphiphilic Cyclic and Linear Peptides Composed of Hydrophobic and Positively-Charged Amino Acids as Antibacterial Agents

机译:由疏水性和带正电荷的氨基酸组成的两亲循环和线性肽作为抗菌剂的设计,合成和评价

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Antimicrobial peptides (AMPs) contain amphipathic structures and are derived from natural resources. AMPs have been found to be effective in treating the infections caused by antibiotic-resistant bacteria (ARB), and thus, are potential lead compounds against ARB. AMPs’ physicochemical properties, such as cationic nature, amphiphilicity, and their size, will provide the opportunity to interact with membrane bilayers leading to damage and death of microorganisms. Herein, AMP analogs of [R4W4] were designed and synthesized by changing the hydrophobicity and cationic nature of the lead compound with other amino acids to provide insights into a structure-activity relationship against selected model Gram-negative and Gram-positive pathogens. Clinical resistant strains of methicillin-resistant Staphylococcus aureus (MRSA) and Escherichia coli (E. coli) were used in the studies. Our results provided information about the structural requirements for optimal activity of the [R4W4] template. When tryptophan was replaced with other hydrophobic amino acids, such as phenylalanine, tyrosine, alanine, leucine, and isoleucine, the antibacterial activities were significantly reduced with MIC values of >128 µg/mL. Furthermore, a change in stereochemistry caused by d-arginine, and use of N-methyltryptophan, resulted in a two-fold reduction of antibacterial activity. It was found that the presence of tryptophan is critical for antibacterial activity, and could not be substituted with other hydrophobic residues. The study also confirmed that cyclic peptides generally showed higher antibacterial activities when compared with the corresponding linear counterparts. Furthermore, by changing tryptophan numbers in the compound while maintaining a constant number of arginine, we determined the optimal number of tryptophan residues to be four, as shown when the number of tryptophan residues increased, a decrease in activity was observed.
机译:抗微生物肽(AMP)包含两亲性结构并从自然资源的。抗菌肽已发现可有效地治疗由耐抗生素的细菌(ARB)的感染,并且因此,反对ARB潜在的先导化合物。放的物理化学性质,如阳离子性质,两亲性,以及它们的大小,将提供机会与膜双层导致损伤和微生物的死亡互动。在此,[R4W4]的AMP类似物,设计并通过改变疏水性和与其它氨基酸的先导化合物的阳离子性质,以提供深入了解针对选择的模型革兰氏阴性菌和革兰氏阳性病原体的结构 - 活性关系合成。耐甲氧西林金黄色葡萄球菌(MRSA)和大肠杆菌(大肠杆菌)的临床耐药株在研究中使用。我们的研究结果提供了有关为[R4W4]模板的最佳活性的结构要求的信息。当色氨酸用其它疏水性氨基酸,如苯丙氨酸,酪氨酸,丙氨酸,亮氨酸和异亮氨酸代替,抗菌活性显著具有> 128微克/毫升的MIC值减少。此外,在立体化学的变化引起的由d精氨酸,和使用N-甲基色氨酸的,导致了两倍的减少抗菌活性。据发现,色氨酸的存在对于抗菌活性关键的,并且不能与其它疏水性残基被取代。研究还证实,当与相应的线性对应物相比,该环肽通常显示出较高的抗菌活性。此外,通过在该化合物改变色氨酸号码,同时保持精氨酸的恒定数目,我们确定色氨酸残基的最佳数量是四,因为观察到活性的降低所示,当色氨酸残基的数量增加,。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号