Author: Shum, Ka To; Tanner, Julian A.
Title: Differential Inhibitory Activities and Stabilisation of DNA Aptamers against the SARS Coronavirus Helicase Cord-id: jumohbcf Document date: 2008_11_21
ID: jumohbcf
Snippet: The helicase from severe acute respiratory syndrome coronavirus (SARSâ€CoV) possesses NTPase, duplex RNA/DNAâ€unwinding and RNAâ€capping activities that are essential for viral replication and proliferation. Here, we have isolated DNA aptamers against the SARSâ€CoV helicase from a combinatorial DNA library. These aptamers show two distinct classes of secondary structure, Gâ€quadruplex and nonâ€Gâ€quadruplex, as shown by circular dichroism and gel electrophoresis. All of the aptamers that
Document: The helicase from severe acute respiratory syndrome coronavirus (SARSâ€CoV) possesses NTPase, duplex RNA/DNAâ€unwinding and RNAâ€capping activities that are essential for viral replication and proliferation. Here, we have isolated DNA aptamers against the SARSâ€CoV helicase from a combinatorial DNA library. These aptamers show two distinct classes of secondary structure, Gâ€quadruplex and nonâ€Gâ€quadruplex, as shown by circular dichroism and gel electrophoresis. All of the aptamers that were selected stimulated ATPase activity of the SARSâ€CoV helicase with lowâ€nanomolar apparent K (m) values. Intriguingly, only the nonâ€Gâ€quadruplex aptamers showed specific inhibition of helicase activities, whereas the Gâ€quadruplex aptamers did not inhibit helicase activities. The nonâ€Gâ€quadruplex aptamer with the strongest inhibitory potency was modified at the 3′â€end with biotin or inverted thymidine, and the modification increased its stability in serum, particularly for the inverted thymidine modification. Structural diversity in selection coupled to postâ€selection stabilisation has provided new insights into the aptamers that were selected for a helicase target. These aptamers are being further developed to inhibit SARSâ€CoV replication.
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