A novel antimicrobial peptide, Ranatuerin-2PLx, showing therapeutic potential in inhibiting proliferation of cancer cells

被引:35
作者
Chen, Xiaoling [1 ]
Zhang, Luyao [1 ]
Ma, Chengbang [1 ]
Zhang, Yingqi [2 ]
Xi, Xinping [1 ]
Wang, Lei [1 ]
Zhou, Mei [1 ]
Burrows, James F. [1 ]
Chen, Tianbao [1 ]
机构
[1] Queens Univ Belfast, Sch Pharm, Belfast BT9 7BL, Antrim, North Ireland
[2] Hebei Med Univ, Dept Emergency Med, Hosp 1, Shijiazhuang 050031, Hebei, Peoples R China
关键词
HOST-DEFENSE PEPTIDES; BIOLOGICAL-ACTIVITIES; FROG-SKIN; APOPTOSIS; IDENTIFICATION; ANTICANCER; EVOLUTION;
D O I
10.1042/BSR20180710
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Antimicrobial peptides are a promising resource for developing novel antibiotic and even anticancer drugs. Here, a 28-mer polypeptide, Ranatuerin-2PLx (R2PLx), was identified from lyophilised skin secretions. The chemically synthetic replicates exhibited moderate and broadspectrum antimicrobial effect against various microorganisms including methicillin-resistant Staphylococcus aureus (MRSA, minimal inhibitory concentration = 256 mu M). In addition, R2PLx was found to inhibit the proliferation of several tumour cells, especially showing more potent effect on prostate cancer cell, PC-3. The early cell apoptosis was observed in 6 h by Annexin V-FITC/propidium iodide staining, as well as the activation of Caspase-3 at 5 mu M peptide concentration. R2PLx may therefore be promising for developing new therapeutic approach for cancer treatment. Moreover, the artificial deficiency of conserved rana-box loop or net positive charge in C-terminal domain notably reduced the biological activities of the truncated and substituted isoforms, respectively, suggesting for maintaining their biological potency of ranatuerin family requires both cysteine-bridged segment and cationincity within the loop domain in C-terminus.
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页数:11
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