Protonation states in SARS-CoV-2 main protease mapped by neutron crystallography

Abstract

The main protease (3CL Mpro) from SARS-CoV-2, the etiological agent of COVID-19, is an essential enzyme for viral replication, possessing an unusual catalytic dyad composed of His41 and Cys145. A long-standing question in the field has been what the protonation states of the ionizable residues in the substrate-binding active site cavity are. Here, we present the room-temperature neutron structure of 3CL Mpro from SARS-CoV-2, which allows direct determination of hydrogen atom positions and, hence, protonation states. The catalytic site natively adopts a zwitterionic reactive state where His41 is doubly protonated and positively charged, and Cys145 is in the negatively charged thiolate state. The neutron structure also identified the protonation states of other amino acid residues, mapping electrical charges and intricate hydrogen bonding networks in the SARS-CoV-2 3CL Mpro active site cavity and dimer interface. This structure highlights the ability of neutron protein crystallography for experimentally determining protonation states at near-physiological temperature — the critical information for structure-assisted and computational drug design.

Protonation State of an Important Histidine from High Resolution Structures of Lytic Polysaccharide Monooxygenases

“…Determining protonation states of residues in proteins experimentally is difficult. Nuclear Magnetic Resonance (NMR) spectroscopy titration and Neutron crystallography are the two most reliable methods [ 36 , 37 , 38 , 39 , 40 ]. While NMR is mostly amenable for small proteins, neutron crystallography is limited by low flux of neutron sources and size of the crystal, among others [ 41 ].…”