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. 2017 Sep 18;9(1-2):192–201. doi: 10.1080/21541248.2017.1346552

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© 2017 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group

This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.

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Figure 2. — Herpesviruses and Rab Proteins. (A) Herpes simplex virus Type 1 (HSV-1) assembly and Rab proteins. HSV-1 utilizes Rab6-dependent TGN-to-PM transport of its glycoproteins, which are subsequently endocytosed in a Rab5-dependent process. Rab11 is essential for re-envelopment of capsids. (B) Human Cytomegalovirus (HCMV) utilization of Rab protein trafficking. Pictured schematically is the CMV assembly compartment, where a series of Rab proteins are recruited and contribute to assembly. Rab6 interacts with the adaptor BicD1 to bring the tegument protein pp150 to the assembly compartment in a dynein-dependent transport process.