The Effect of Distal Interactions on O2-Binding to Heme

Kasper Planeta Kepp, Pouria Dasmeh

Research output: Contribution to journalJournal articleResearchpeer-review

Abstract

This paper reports DFT-computed electronic ground states, Mössbauer isomer shifts, O-O and Fe-O vibration frequencies, and thermodynamics of O2-binding of heme models representing different distal (position E7) interactions, strictly validated against experimental data. Based on the results, the impact of specific types of distal interactions on oxyheme electronic structure can be systematized. Hydrogen bonding increases back donation, O-O bond activation, and oxygen binding affinity. The heme side-chains reduce isomer shifts by -0.06 mm/s due to electron-withdrawal from iron, and distal hydrogen bonds can further reduce isomer shifts up to 0.07 mm/s. The O-O stretch vibration, the O-O distance, and the isomer shift possess substantial heuristic value in interpreting electronic structure, whereas other properties are less effective, based on computed correlation coefficients. Shorter Fe-O bond length does not correlate with O2-affinity, as hydrogen bonding elongates both Fe-O and O-O bonds by ~0.01-0.02 Å, contrary to the situation absent of distal hydrogen bonds and of potential relevance to ligand-activation where distal interactions are involved. An ionic (Weiss-type) model of Fe-O bonding combined with electron withdrawal by hydrogen bonds is shown to robustly explain the structural, spectroscopic, and thermodynamic properties of the hemes. The identified correlations may be useful e.g. for designing O2-activating catalysts or for diagnosing heme protein variants.
Original languageEnglish
JournalJournal of Physical Chemistry Part B: Condensed Matter, Materials, Surfaces, Interfaces & Biophysical
Volume117
Issue number14
Pages (from-to)3755-3770
ISSN1520-6106
DOIs
Publication statusPublished - 2013

Fingerprint Dive into the research topics of 'The Effect of Distal Interactions on O2-Binding to Heme'. Together they form a unique fingerprint.

Cite this