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. 2019 Jul 4;9:9711. doi: 10.1038/s41598-019-45910-9

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© The Author(s) 2019

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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VIR-CLASP demonstrates that EMC4 is required for ZIKV entry and uncoating. SDS-PAGE and silver stain (top), or immunoblot (bottom) of VIR-CLASP performed on HA-EMC4 CRISPR knock-in (WT) or knockout (KO) HuH-7 cells infected with unlabeled or 4SU-labeled ZIKV. Baf, 200 nM bafilomycin for 1 hr; XL, virus was pre-crosslinked with UV_365nm. The western blots are from the same gel and the image was cropped to show HA-EMC4, FMR1, ELAVL1, YTHFDF1, and TUBA4A.