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• W2007546430 abstract "During egress from the nucleus, HSV capsids that contain DNA (termed C capsids) are preferentially enveloped at the inner nuclear membrane over capsid types lacking DNA. Using coimmunoprecipitation and biochemical analyses of wild-type and mutant capsids, we identify an interaction between a complex of pU L 17/pU L 25, termed the C capsid-specific complex (CCSC), and pU L 31, a component of the nuclear egress complex (NEC). We also show that the interactions between these components are dependent on expression of all three proteins but occur independently of the pU L 31 interacting protein and NEC component pU L 34, as well as a kinase encoded by U S 3 that phosphorylates both pU L 31 and pU L 34. The interaction between the CCSC and pU L 31 in the NEC suggests a mechanism to conserve viral resources by promoting assembly of only those viral particles with the potential to become infectious." @default.
• W2007546430 created "2016-06-24" @default.
• W2007546430 creator A5044944660 @default.
• W2007546430 creator A5050705644 @default.
• W2007546430 date "2011-08-05" @default.
• W2007546430 modified "2023-10-10" @default.
• W2007546430 title "Selection of HSV capsids for envelopment involves interaction between capsid surface components pU _L 31, pU _L 17, and pU _L 25" @default.
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• W2007546430 doi "https://doi.org/10.1073/pnas.1108564108" @default.
• W2007546430 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3161533" @default.
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