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人CAP18肽的抗菌活性。

Anti-microbial activity of human CAP18 peptides.

作者信息

Larrick J W, Hirata M, Zhong J, Wright S C

机构信息

Palo Alto Institute of Molecular Medicine, Mountain View, CA 94043, USA.

出版信息

Immunotechnology. 1995 May;1(1):65-72. doi: 10.1016/1380-2933(95)00006-2.

Abstract

BACKGROUND

CAP18 derived from rabbit leukocytes is a 142-amino acid protein recently demonstrated to have Lipopolysaccharide (LPS) binding and anti-microbial activity. The C-terminal 37 amino acids of rabbit CAP18 (CAP18(106-142) comprise the LPS-binding and anti-microbial domain. The homologous domain of human CAP18 (huCAP18(104-140) was identified from the recently cloned human CAP18 cDNA.

OBJECTIVES

To evaluate the antimicrobial activity of C-terminal peptides derived from human CAP18.

STUDY DESIGN

Prepare synthetic human CAP18(104-140) and study anti-microbial activity versus various gram-negative and gram-positive bacteria.

RESULTS

Synthetic human CAP18(104-140) has broad anti-microbial activity versus both gram-positive (IC50 = 2.5 micrograms/ml) and gram-negative bacteria (IC50 = 0.5-5 micrograms/ml). Susceptible strains include Staphylococcus aureus, Klebsiella pneumoniae, Escherichia coli, Pseudomonas aeruginosa and Salmonella typhimurium. A 32-amino acid peptide lacking five amino acids from the C-terminus of CAP18(104-140) has higher activity. Unlike previously characterized anti-microbial peptides derived from granulocyte proteins, CAP18(104-140) is active in serum.

CONCLUSIONS

Human CAP18(104-140) or a derivative peptide may have therapeutic potential for bacterial sepsis.

摘要

背景

源自兔白细胞的CAP18是一种含142个氨基酸的蛋白质,最近证明其具有脂多糖(LPS)结合和抗菌活性。兔CAP18的C末端37个氨基酸(CAP18(106 - 142))构成LPS结合和抗菌结构域。从最近克隆的人CAP18 cDNA中鉴定出了人CAP18的同源结构域(huCAP18(104 - 140))。

目的

评估源自人CAP18的C末端肽的抗菌活性。

研究设计

制备合成的人CAP18(104 - 140),并研究其对各种革兰氏阴性菌和革兰氏阳性菌的抗菌活性。

结果

合成的人CAP18(104 - 140)对革兰氏阳性菌(IC50 = 2.5微克/毫升)和革兰氏阴性菌(IC50 = 0.5 - 5微克/毫升)均具有广泛的抗菌活性。敏感菌株包括金黄色葡萄球菌、肺炎克雷伯菌、大肠杆菌、铜绿假单胞菌和鼠伤寒沙门氏菌。一种从CAP18(104 - 140)的C末端缺失五个氨基酸的32个氨基酸的肽具有更高的活性。与先前表征的源自粒细胞蛋白的抗菌肽不同,CAP18(104 - 140)在血清中具有活性。

结论

人CAP18(104 - 140)或其衍生肽可能对细菌性败血症具有治疗潜力。

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