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Discovery of Small-Molecule Inhibitors Targeting the E3 Ubiquitin Ligase Activity of the Herpes Simplex Virus 1 ICP0 Protein Using an In Vitro High-Throughput Screening Assay

Title: Discovery of Small-Molecule Inhibitors Targeting the E3 Ubiquitin Ligase Activity of the Herpes Simplex Virus 1 ICP0 Protein Using an In Vitro High-Throughput Screening Assay
Authors: Deschamps, Thibaut; Waisner, Hope; Dogrammatzis, Christos; Roy, Anuradha; Chacko, Shibin; Perera, Chamani; Prisinzano, Thomas E.; Kalamvoki, Maria
Contributors: Sandri-Goldin, Rozanne M.; HHS | NIH | National Institute of General Medical Sciences
Source: Journal of Virology ; volume 93, issue 13 ; ISSN 0022-538X 1098-5514
Publisher Information: American Society for Microbiology
Publication Year: 2019
Description: Since acyclovir and its derivatives were launched for herpesviruses control almost four decades ago, the search for novel antivirals has waned. However, as human life expectancy has increased, so has the number of immunocompromised individuals who receive prolonged treatment for HSV recurrences. This has led to an increase in unresponsive patients due to acquired viral drug resistance. Thus, novel treatments need to be explored. Here we explored the HSV-1 ICP0 E3 ligase as a potential antiviral target because (i) ICP0 is expressed before virus replication, (ii) it is essential for infection in vivo , (iii) it is required for efficient reactivation of the virus from latency, (iv) inhibition of its E3 ligase activity would sustain host immune responses, and (v) it is shared by other herpesviruses. We report a compound that inhibits HSV-1 infection in an ICP0-dependent manner by inhibiting ICP0 E3 ligase activity.
Document Type: article in journal/newspaper
Language: English
DOI: 10.1128/jvi.00619-19
DOI: 10.1128/JVI.00619-19
Availability: https://doi.org/10.1128/jvi.00619-19; https://journals.asm.org/doi/pdf/10.1128/JVI.00619-19
Rights: https://journals.asm.org/non-commercial-tdm-license
Accession Number: edsbas.DE32CE2D
Database: BASE