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Structure · dataset · 2026

<p>The G protein of low-temperature-sensitive <i>rhabdovirus</i> is palmitoylated.</p>

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<p><b>(A)</b> Protein palmitoylation software CSS-palm 4.0 was used to predict the VHSV G, IHNV G, SVCV G, MSRV G palmitoylation sites. <b>(B)</b> ZF4 cells were transfected with plasmids expressing VHSV G/WT and VHSV G(C/A) at 16 °C and subsequently mock treated (VHSV G/WT and VHSV G(C/A) groups) or treated with 50 μM 2-BP (VHSV G/WT 2-BP group). Protein palmitoylation was examined by IP-ABE assay in the presence and absence of HAM.

The palmitoylated VHSV G and the immunoprecipitated VHSV G were blotted by HRP-streptavidin and His mAb, respectively. <b>(C)</b> ZF4 cells were transfected with plasmids expressing IHNV G/WT and IHNV G(C/A) at 16 °C and subsequently mock treated (IHNV G/WT and IHNV G(C/A) groups) or treated with 50 μM 2-BP (IHNV G/WT 2-BP group). Protein palmitoylation was examined by IP-ABE assay in the presence and absence of HAM. The palmitoylated IHNV G and the immunoprecipitated IHNV G were blotted by HRP-streptavidin and His mAb, respectively. <b>(D-F)</b> ZF4 cells were transfected with plasmids expressing VHSV G, IHNV G and MSRV G at 16 °C and 28 °C. Protein palmitoylation was examined by IP-ABE assay in the presence of HAM.

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The palmitoylated MSRV G, VHSV G and IHNV G and the immunoprecipitated VHSV G, IHNV G and MSRV G were blotted by HRP-streptavidin and His mAb, respectively. <b>(G-H)</b> ZF4 cells were transfected with the plasmid encoding VHSV G for 24h at 28 °C and 16 °C. Then, the cells were stimulated with CHX (1 µg/mL) and lysed at the indicated time points (0 h, 1 h, 2 h, and 4 <b>h)</b>. The protein levels of VHSV G in the cell lysate were measured by Western blotting. <b>(I-J)</b> ZF4 cells were transfected with the plasmid encoding IHNV G for 24h at 28 °C and 16 °C. Then, the cells were stimulated with CHX (1 µg/mL) and lysed at the indicated time points (0 h, 1 h, 2 h, and 4 <b>h)</b>.

The protein levels of IHNV G in the cell lysate were measured by Western blotting. <b>(K)</b> ZF4 cells were transfected with the plasmid encoding MSRV G and were then treated with Orlistat (25µM, 50 µM, and 100 µM) or DMSO for 24 h at 16 °C. The MSRV G protein levels were measured by Western blotting. <b>(L)</b> ZF4 cells were transfected with the plasmid encoding MSRV G and were then treated with 2-BP (25µM, 50 µM, and 100 µM) or DMSO for 24 h at 16 °C. The MSRV G protein levels were measured by Western blotting. <b>(M-N)</b> ZF4 cells were transfected with the plasmid encoding VHSV G and IHNV G and were then treated with Orlistat (25µM, 50 µM, and 100 µM) or DMSO for 24 h at 16 °C. The VHSV G and IHNV G protein levels were measured by Western blotting. <b>(O-P)</b> ZF4 cells were transfected with the plasmid encoding VHSV G and IHNV G and were then treated with 2-BP (25µM, 50 µM, and 100 µM) or DMSO for 24 h at 16 °C. The VHSV G and IHNV G protein levels were measured by Western blotting.</p>

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