Lu Yongzhong, Qiu Qian, Li Chen, Cheng Linyue, Liu Jie
Shandong Provincial Key Laboratory of Biochemical Engineering, Qingdao University of Science and Technology, No. 53, Zhengzhou Road, 266042, Qingdao, China.
Yellow Sea Fisheries Research Institute, Chinese Academy Of Fishery Sciences, No. 106, Nanjing Road, 266071, Qingdao, China.
Aquac Rep. 2019 Jul;14:100195. doi: 10.1016/j.aqrep.2019.100195. Epub 2019 Apr 15.
Since effective chemotherapeutics or preventive measures are still unavailable, finding feasible approaches against white spot syndrome virus (WSSV) has always been the vital subject in shrimp farming field. Envelope proteins are the ideal targets for antiviral strategies development due to their indispensable roles in virus entry, and inhibitory peptides targeting them have been proved to be promising in blocking virus infection. In this study, the Wimley-White interfacial hydrophobicity scale (WWIHS) in combination with known structural data was applied to identify potential inhibitory peptides that targeted the envelope protein VP28 of WSSV. Results showed that two potential inhibitory peptides were identified, one of which exhibited not only obvious antiviral activity, but also broad-spectrum antimicrobial activity. The inhibitory peptide identified here can serve as a lead compound for anti-WSSV strategies development.
由于目前仍缺乏有效的化学治疗药物或预防措施,因此寻找对抗白斑综合征病毒(WSSV)的可行方法一直是对虾养殖领域的重要课题。包膜蛋白在病毒进入过程中发挥着不可或缺的作用,是抗病毒策略开发的理想靶点,针对包膜蛋白的抑制性肽已被证明在阻断病毒感染方面具有潜力。在本研究中,结合已知的结构数据,应用Wimley-White界面疏水性标度(WWIHS)来鉴定针对WSSV包膜蛋白VP28的潜在抑制性肽。结果表明,鉴定出了两种潜在的抑制性肽,其中一种不仅表现出明显的抗病毒活性,还具有广谱抗菌活性。此处鉴定出的抑制性肽可作为抗WSSV策略开发的先导化合物。