Isolation and characterization of 2 '-F-RNA aptamers against whole HIV-1 subtype C envelope pseudovirus

作者：London Grace M; Mayosi Bongani M; Khati Makobetsa^*

来源：Biochemical and Biophysical Research Communications, 2015, 456(1): 428-433.

DOI：10.1016/j.bbrc.2014.11.101

• HIV-1
• Enveloped pseudotyped virus
• Entry inhibition
• SELEX
• Aptamers

Aptamers, which are artificial nucleic acid ligands akin to antibodies in function, represent a new class of molecules that can prevent HIV infection. In this study, we isolated RNA aptamers against whole HV-1(CAP45) enveloped pseudotyped virus, with a view to target surface molecules that facilitate infection, such as the envelope protein, in their native form. HIV-1(CAP45) belongs to subtype C viruses endemic in Sub-Saharan Africa and responsible for the majority of the global HIV-1 infections. After nine rounds of the systematic evolution of ligands by exponential enrichment (SELEX) method, we isolated twenty-three aptamer clones that inhibited infection of target cells by HIV-1 CANS with 50% inhibitory concentration (lC(50)) values of 0.1-50 nM. Four of these aptamers called CSIR1.1, CSIR1.4, CSIR1.5 and CSIR1.6 bound to gp120 with affinity constant (K-D) values between 16.9 and 195 nM and one aptamer called CSIR1.2 bound gp41. Interestingly, one aptamer called CSIR1.3 that did not bind gp120 or gp41 also inhibited infection of the target cells by HIV-1 corms with IC50 of less than 5 nM. Taken together, these data show that the aptamers inhibit infection of HIV-1(CAP45) by binding to gp120 or gp41, or other viral surface molecules necessary for infection. The results argue in favour of using these aptamers as analytical tools to further probe HIV-1 entry, and their future development as HIV-1 entry inhibitors.

• 出版日期2015-1-2