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A New Crystal Form of the SARS-CoV-2 Receptor Binding Domain: CR3022 Complex-An Ideal Target for In-Crystal Fragment Screening of the ACE2 Binding Site Surface.
Nichols, Charlie; Ng, Joseph; Keshu, Annika; Fraternali, Franca; De Nicola, Gian F.
  • Nichols C; British Heart Foundation Centre of Excellence, Department of Cardiology, Rayne Institute, St Thomas' Hospital, King's College London, London, United Kingdom.
  • Ng J; The Randall Centre for Cell and Molecular Biophysics, New Hunt's House, King's College London, London, United Kingdom.
  • Keshu A; British Heart Foundation Centre of Excellence, Department of Cardiology, Rayne Institute, St Thomas' Hospital, King's College London, London, United Kingdom.
  • Fraternali F; British Heart Foundation Centre of Excellence, Department of Cardiology, Rayne Institute, St Thomas' Hospital, King's College London, London, United Kingdom.
  • De Nicola GF; British Heart Foundation Centre of Excellence, Department of Cardiology, Rayne Institute, St Thomas' Hospital, King's College London, London, United Kingdom.
Front Pharmacol ; 11: 615211, 2020.
Article in English | MEDLINE | ID: covidwho-1389230
ABSTRACT
In-crystal fragment screening is a powerful tool to chemically probe the surfaces used by proteins to interact, and identify the chemical space worth exploring to design protein-protein inhibitors. A crucial prerequisite is the identification of a crystal form where the target area is exposed and accessible to be probed by fragments. Here we report a crystal form of the SARS-CoV-2 Receptor Binding Domain in complex with the CR3022 antibody where the ACE2 binding site on the Receptor Binding Domain is exposed and accessible. This crystal form of the complex is a valuable tool to develop antiviral molecules that could act by blocking the virus entry in cells.
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Full text: Available Collection: International databases Database: MEDLINE Language: English Journal: Front Pharmacol Year: 2020 Document Type: Article Affiliation country: FPHAR.2020.615211

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Full text: Available Collection: International databases Database: MEDLINE Language: English Journal: Front Pharmacol Year: 2020 Document Type: Article Affiliation country: FPHAR.2020.615211