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Peptide and peptide-based inhibitors of SARS-CoV-2 entry.
Schütz, Desiree; Ruiz-Blanco, Yasser B; Münch, Jan; Kirchhoff, Frank; Sanchez-Garcia, Elsa; Müller, Janis A.
  • Schütz D; Institute of Molecular Virology, Ulm University Medical Center, 89081 Ulm, Germany.
  • Ruiz-Blanco YB; Computational Biochemistry, Center of Medical Biotechnology, University of Duisburg-Essen, 45117 Essen, Germany.
  • Münch J; Institute of Molecular Virology, Ulm University Medical Center, 89081 Ulm, Germany.
  • Kirchhoff F; Institute of Molecular Virology, Ulm University Medical Center, 89081 Ulm, Germany.
  • Sanchez-Garcia E; Computational Biochemistry, Center of Medical Biotechnology, University of Duisburg-Essen, 45117 Essen, Germany. Electronic address: elsa.sanchez-garcia@uni-due.de.
  • Müller JA; Institute of Molecular Virology, Ulm University Medical Center, 89081 Ulm, Germany. Electronic address: janis.mueller@uni-ulm.de.
Adv Drug Deliv Rev ; 167: 47-65, 2020 12.
Article in English | MEDLINE | ID: covidwho-921794
ABSTRACT
To date, no effective vaccines or therapies are available against the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative pandemic agent of the coronavirus disease 2019 (COVID-19). Due to their safety, efficacy and specificity, peptide inhibitors hold great promise for the treatment of newly emerging viral pathogens. Based on the known structures of viral proteins and their cellular targets, antiviral peptides can be rationally designed and optimized. The resulting peptides may be highly specific for their respective targets and particular viral pathogens or exert broad antiviral activity. Here, we summarize the current status of peptides inhibiting SARS-CoV-2 entry and outline the strategies used to design peptides targeting the ACE2 receptor or the viral spike protein and its activating proteases furin, transmembrane serine protease 2 (TMPRSS2), or cathepsin L. In addition, we present approaches used against related viruses such as SARS-CoV-1 that might be implemented for inhibition of SARS-CoV-2 infection.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Antiviral Agents / Peptide Fragments / SARS-CoV-2 / COVID-19 / COVID-19 Drug Treatment Topics: Vaccines Limits: Humans Language: English Journal: Adv Drug Deliv Rev Journal subject: Pharmacology / Drug Therapy Year: 2020 Document Type: Article Affiliation country: J.addr.2020.11.007

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Antiviral Agents / Peptide Fragments / SARS-CoV-2 / COVID-19 / COVID-19 Drug Treatment Topics: Vaccines Limits: Humans Language: English Journal: Adv Drug Deliv Rev Journal subject: Pharmacology / Drug Therapy Year: 2020 Document Type: Article Affiliation country: J.addr.2020.11.007