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文献详情 >De novo Design of a Leu-Arg-rich An... 收藏
De novo Design of a Leu-Arg-rich Antimicrobial Peptide

De novo Design of a Leu-Arg-rich Antimicrobial Peptide

作     者:MA Qing-quan SHAN An-shan DONG Na CAO Yan-ping 

作者机构:(Institute of Animal Nutrition Northeast Agricultural University Harbin 150030 China) 

出 版 物:《畜牧兽医学报》 (ACTA VETERINARIA ET ZOOTECHNICA SINICA)

年 卷 期:2011年第42卷第B12期

页      码:20-23页

摘      要:Antimicrobial peptides may be regarded as a potential source of future antibiotics, and the modes of action have implicated the cationic and hydrophobic nature of their interaction with bacterial membranes. In the present study, a 16-residue peptide (LGR16) was developed with the aim of examining the feasibility of designing an antimicrobial peptide by segregating hydrophobic residues in the nonpolar side and positively charged residues in the polar side, based on the helical wheel projections. Antimicrobial activity, hemolytic activity, cytotoxicity against mammalian cells and bactericidal kinetics were investigated to fully evaluate the biological function of the peptide. The results showed that the peptide LGR16 had strong antimicrobial activity, and its MICs against Gram-negative and Gram-positive bacteria were 8 and 4 μg/mL, respectively. LGR16 also exhibited rapid bactericidal action and had totally eradicated the bacteria at 10 min. LGR16 showed only weak hemolysis against chicken red blood cells and cytotoxicity aginst Vero cells at its MICs, and the concentration that caused 50% hemolysis exceeded its MICs 8-fold. Overall, antimicrobial peptides can be designed by assembling hydrophobic residues in the hydrophobic side and basic residues in the opposite side. The peptide LGR16 may be developed as a prospective candidate for an antimicrobial drug.

主 题 词:从头设计 抗菌肽 亮氨酸 精氨酸 溶血活性 哺乳动物细胞 革兰氏阳性菌 革兰氏阴性菌 

学科分类:0710[理学-生物科学类] 090601[090601] 071010[071010] 081704[081704] 07[理学] 08[工学] 0817[工学-轻工类] 09[农学] 0906[农学-水产类] 

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馆 藏 号:203342325...

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