ยฉ The Author(s) 2019. Published by Oxford University Press on behalf of Nucleic Acids Research. To date, an effective therapeutic treatment that confers strong attenuation toward coronaviruses (Co. Vs) remains elusive. Of all the potential drug targets, the helicase of Co. Vs is considered to be one of the most important. Here, we first present the structure of the full-length Nsp13 helicase of SARS-CoV (SARS-Nsp13) and investigate the structural coordination of its five domains and how these contribute to its translocation and unwinding activity. A translocation model is proposed for the Upf1-like helicase members according to three different structural conditions in solution characterized through H/D exchange assay, including substrate state (SARS-Nsp13-dsDNA bound with AMPPNP), transition state (bound with ADP-AlF4-) and product state (bound with ADP). We observed that the ฮฒ19-ฮฒ20 loop on the 1A domain is involved in unwinding process directly. Furthermore, we have shown that the RNA dependent RNA polymerase (Rd. Rp), SARS-Nsp12, can enhance the helicase activity of SARS-Nsp13 through interacting with it directly. The interacting regions were identified and can be considered common across Co. Vs, which provides new insights into the Replication and Transcription Complex (RTC) of Co. Vs.
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