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. 2020 Jul 28;182(6):1560–1573.e13. doi: 10.1016/j.cell.2020.07.033

Figure 1.

Figure 1

SARS-CoV-2 nsp13 Helicase Forms a Stable Complex with the Holo-RdRp and an RNA Scaffold

(A) The RNA scaffold used for biochemistry, native mass spectrometry (nMS), and cryo-EM.

(B) A native gel electrophoretic mobility shift assay reveals that nsp13 forms a stable complex with holo-RdRp:RNA. The 4.5% polyacrylamide gel was visualized with Gel Red to stain the RNA.

(C) nMS spectra and the corresponding deconvolved spectra for the holo-RdRp containing the RNA scaffold (A) with and without nsp13. The measured mass for the holo-RdRp:RNA complex corroborates the established stoichiometry of 1:2:1:1 for nsp7:nsp8:nsp12:RNA (Hillen et al., 2020; Kirchdoerfer and Ward, 2019; Wang et al., 2020; Yin et al., 2020), respectively (bottom). Addition of the 67.5-kDa nsp13 helicase to the RNA-bound holo-RdRp sample forms a transcription complex/helicase assembly with 1:1 stoichiometry (top).

See also Figures S1 and S2.

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