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鉴定与HIV-1 gp120 V3环相互作用的Epap-1潜在区域。

Identification of the potential regions of Epap-1 that interacts with V3 loop of HIV-1 gp120.

作者信息

Bhaskar C, Reddy Palakolanu S, Chandra K Sarath, Sabde Sudeep, Mitra Debashis, Kondapi Anand K

机构信息

Department of Biotechnology, University of Hyderabad, Hyderabad, Andhra Pradesh, India.

出版信息

Biochim Biophys Acta. 2013 Apr;1834(4):780-90. doi: 10.1016/j.bbapap.2013.01.017. Epub 2013 Jan 27.

DOI:10.1016/j.bbapap.2013.01.017
PMID:23360764
Abstract

Early pregnancy associated protein-1 (Epap-1), a 90kDa glycoprotein present in first trimester placental tissue, inhibits HIV-1 entry through interaction with HIV-1 gp120 at V3 and C5 regions. In the present study, we have identified the specific 32 mer region of Epap-1 that can interact with V3 loop. This was achieved by docking between Epap-1 molecular model and gp120 and studying the interaction of peptides with gp120 in vitro. Out of four peptides analyzed, two peptides (P-2 and P-3) showed significant interaction with V3 domain (N=8; N=7) of gp120. In the studies conducted using soluble gp120 and virus, peptide P-2 has shown conserved interaction at V3 loop regions recognized by 257D and F425 antibodies and higher anti-viral activity. Also, P-2 inhibited cell fusion mediated dye transfer between gp120 expressing HL2/3 and CD4 expressing Sup T1 cells suggesting its inhibition of viral entry, which is further confirmed by its action on HIV infection mediated by Tat activated beta gal expression in TZM-bl cells. Further optimization of P-2 peptide showed that the anti-viral activity and gp120 interaction residues lie in the N-terminal region of the peptide. These results together suggest that P-2 inhibits viral entry through specific interaction at V3 loop region.

摘要

早孕相关蛋白-1(Epap-1)是一种存在于孕早期胎盘组织中的90kDa糖蛋白,它通过在V3和C5区域与HIV-1 gp120相互作用来抑制HIV-1进入。在本研究中,我们确定了Epap-1中可与V3环相互作用的特定32肽区域。这是通过Epap-1分子模型与gp120对接,并在体外研究肽与gp120的相互作用来实现的。在分析的四种肽中,两种肽(P-2和P-3)与gp120的V3结构域(N = 8;N = 7)表现出显著相互作用。在使用可溶性gp120和病毒进行的研究中,肽P-2在257D和F425抗体识别的V3环区域表现出保守的相互作用和更高的抗病毒活性。此外,P-2抑制了表达gp120的HL2/3细胞与表达CD4的Sup T1细胞之间的细胞融合介导的染料转移,表明其对病毒进入的抑制作用,这在其对TZM-bl细胞中由Tat激活的β半乳糖苷酶表达介导的HIV感染的作用中得到进一步证实。对P-2肽的进一步优化表明,抗病毒活性和与gp120相互作用的残基位于该肽的N端区域。这些结果共同表明,P-2通过在V3环区域的特异性相互作用抑制病毒进入。

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