The open archive for STFC research publications

Full Record Details

Persistent URL http://purl.org/net/epubs/work/12098399
Record Status Checked
Record Id 12098399
Title Renormalization of myoglobin–ligand binding energetics by quantum many-body effects
Abstract We carry out a first-principles atomistic study of the electronic mechanisms of ligand binding and discrimination in the myoglobin protein. Electronic correlation effects are taken into account using one of the most advanced methods currently available, namely a linear-scaling density functional theory (DFT) approach wherein the treatment of localized iron 3d electrons is further refined using dynamical mean-field theory. This combination of methods explicitly accounts for dynamical and multireference quantum physics, such as valence and spin fluctuations, of the 3d electrons, while treating a significant proportion of the protein (more than 1,000 atoms) with DFT. The computed electronic structure of the myoglobin complexes and the nature of the Fe–O2 bonding are validated against experimental spectroscopic observables. We elucidate and solve a long-standing problem related to the quantum-mechanical description of the respiration process, namely that DFT calculations predict a strong imbalance between O2 and CO binding, favoring the latter to an unphysically large extent. We show that the explicit inclusion of the many-body effects induced by the Hund’s coupling mechanism results in the correct prediction of similar binding energies for oxy- and carbonmonoxymyoglobin.
Organisation STFC , HC
Funding Information
Related Research Object(s):
Language English (EN)
Type Details URI(s) Local file(s) Year
Journal Article P Natl Acad Sci USA 111, no. 16 (2014): 5790-5795. doi:10.1073/pnas.1322966111 2014
Showing record 1 of 1
Science and Technology Facilities Council Switchboard: 01793 442000