Author: Laine, Romain F.; Albecka, Anna; van de Linde, Sebastian; Rees, Eric J.; Crump, Colin M.; Kaminski, Clemens F.
Title: Structural analysis of herpes simplex virus by optical super-resolution imaging Document date: 2015_1_22
ID: 0zchxz00_8
Snippet: As shown in the top row in Fig. 1a , for every fluorophore combination tested, two-colour dSTORM consistently demonstrated the envelope protein gD to be located at larger radial distance than the tegument protein VP16. The two tegument proteins VP16 and pUL37 showed a large overlap and similar radial distributions, suggesting that VP16 and pUL37 reside in the same region of the tegument layer (Fig. 1a , bottom row). The inner tegument protein VP1.....
Document: As shown in the top row in Fig. 1a , for every fluorophore combination tested, two-colour dSTORM consistently demonstrated the envelope protein gD to be located at larger radial distance than the tegument protein VP16. The two tegument proteins VP16 and pUL37 showed a large overlap and similar radial distributions, suggesting that VP16 and pUL37 reside in the same region of the tegument layer (Fig. 1a , bottom row). The inner tegument protein VP1/2 and the outer tegument protein VP16 are thought to reside at different radial locations, with VP1/2 expected to lie closer to the capsid than VP16. However, by resolving and analysing individual virus particles, we could not consistently differentiate between outer and inner tegument, irrespective of dye combination used (Fig. 1a , bottom row, second and third panel).
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