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

机译:疏水和带正电荷氨基酸作为抗菌剂的两亲环肽和线性肽的设计合成和评价

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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:抗菌肽(AMPs)包含两亲结构,并且来源于自然资源。已发现AMP可有效治疗由抗生素抗性细菌(ARB)引起的感染,因此是抗ARB的潜在先导化合物。 AMP的物理化学特性(例如阳离子性质,两亲性及其大小)将提供与膜双层相互作用的机会,从而导致微生物的破坏和死亡。本文中,通过改变先导化合物与其他氨基酸的疏水性和阳离子性质,设计和合成了[R4W4]的AMP类似物,以提供针对所选革兰氏阴性和革兰氏阳性病原体的构效关系的见解。在研究中使用耐甲氧西林金黄色葡萄球菌(MRSA)和大肠杆菌(E. coli)的临床耐药菌株。我们的结果提供了有关[R4W4]模板最佳活性的结构要求的信息。当色氨酸被其他疏水性氨基酸取代时,例如苯丙氨酸,酪氨酸,丙氨酸,亮氨酸和异亮氨酸,其抗菌活性显着降低,MIC值> 128 µg / mL。此外,由d-精氨酸引起的立体化学变化以及使用N-甲基色氨酸导致抗菌活性降低了两倍。发现色氨酸的存在对于抗菌活性至关重要,并且不能被其他疏水残基取代。研究还证实,与相应的线性对应物相比,环肽通常显示出更高的抗菌活性。此外,通过改变化合物中的色氨酸数目,同时保持恒定的精氨酸数目,我们确定色氨酸残基的最佳数目为四个,如当色氨酸残基数目增加时观察到的活性降低。

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