DOE PAGES title logo U.S. Department of Energy
Office of Scientific and Technical Information

Title: Electric fields imbue enzyme reactivity by aligning active site fragment orbitals

Journal Article · · Proceedings of the National Academy of Sciences of the United States of America

It is broadly recognized that intramolecular electric fields, produced by the protein scaffold and acting on the active site, facilitate enzymatic catalysis. This field effect can be described by several theoretical models, each of which is intuitive to varying degrees. In this contribution, we show that a fundamental effect of electric fields is to generate electrostatic potentials that facilitate the energetic alignment of reactant frontier orbitals. We apply this model to demystify the impact of electric fields on high-valent iron–oxo heme proteins: catalases, peroxidases, and peroxygenases/monooxygenases. Specifically, we show that this model easily accounts for the observed field-induced changes to the spin distribution within peroxidase active sites and explains the transition between epoxidation and hydroxylation pathways seen in Cytochrome P450 active site models. Thus, for the intuitive interpretation of the chemical effect of the field, the strategy involves analyzing the response of the orbitals of active site fragments, and their energetic alignment. We note that the energy difference between fragment orbitals involved in charge redistribution acts as a measure for the chemical hardness/softness of the reactive complex. This measure, and its sensitivity to electric fields, offers a single parameter model from which to quantitatively assess the effects of electric fields on reactivity and selectivity. Thus, the model provides an additional perspective to describe electrostatic preorganization and offers ways for its manipulation.

Research Organization:
Los Alamos National Laboratory (LANL), Los Alamos, NM (United States)
Sponsoring Organization:
NSF-CHE (National Science Foundation); USDOE Laboratory Directed Research and Development (LDRD) Program
Grant/Contract Number:
89233218CNA000001
OSTI ID:
2476039
Report Number(s):
LA-UR--24-25778
Journal Information:
Proceedings of the National Academy of Sciences of the United States of America, Journal Name: Proceedings of the National Academy of Sciences of the United States of America Journal Issue: 44 Vol. 121; ISSN 0027-8424
Publisher:
National Academy of SciencesCopyright Statement
Country of Publication:
United States
Language:
English

References (33)

Optimized Slater-type basis sets for the elements 1-118 journal May 2003
Chemistry with ADF journal January 2001
External electric field effects on chemical structure and reactivity journal July 2019
A comparison of correlation-consistent and Pople-type basis sets journal October 1995
Hard and soft acids and bases—the evolution of a chemical concept journal April 1990
A single crystal study of the silver-catalysed selective oxidation and total oxidation of ethylene journal April 1985
The Nature and Reactivity of Ferryl Heme in Compounds I and II journal January 2018
Oxygen Activation and Radical Transformations in Heme Proteins and Metalloporphyrins journal December 2017
Local Electric Fields As a Natural Switch of Heme-Iron Protein Reactivity journal May 2021
Designing a Built-In Electric Field for Efficient Energy Electrocatalysis journal December 2022
Tuning Molecular Orbitals in Molecular Electronics and Spintronics journal September 2009
The Asp-His-iron triad of cytochrome c peroxidase controls the reduction potential electronic structure, and coupling of the tryptophan free radical to the heme journal April 1993
Electrostatic Basis for Enzyme Catalysis journal August 2006
Heme Enzyme Structure and Function journal January 2014
Heme-Containing Oxygenases journal January 1996
A Rational Basis for the Axial Ligand Effect in C−H Oxidation by [MnO(porphyrin)(X)] + (X = H 2 O, OH , O 2− ) from a DFT Study journal September 2008
Ab Initio Calculation of Vibrational Absorption and Circular Dichroism Spectra Using Density Functional Force Fields journal November 1994
An empirical valence bond approach for comparing reactions in solutions and in enzymes journal September 1980
Electrostatic catalysis of ionic aggregates. I. Ionization and dissociation of trityl chloride and hydrogen chloride in lithium perchlorate-diethyl ether solutions journal April 1970
Field-Dependent Electrode−Chemisorbate Bonding:  Sensitivity of Vibrational Stark Effect and Binding Energetics to Nature of Surface Coordination journal March 2002
External Electric Field Will Control the Selectivity of Enzymatic-Like Bond Activations journal September 2004
Designed Local Electric Fields─Promising Tools for Enzyme Engineering journal December 2023
What Affects the Quartet−Doublet Energy Splitting in Peroxidase Enzymes? journal November 2005
Production of the antimalarial drug precursor artemisinic acid in engineered yeast journal April 2006
Electrostatic catalysis of a Diels–Alder reaction journal March 2016
Oriented electric fields as future smart reagents in chemistry journal November 2016
A two-directional vibrational probe reveals different electric field orientations in solution and an enzyme active site journal May 2022
Computational optimization of electric fields for better catalysis design journal September 2018
Harnessing electrostatic catalysis in single molecule, electrochemical and chemical systems: a rapidly growing experimental tool box journal January 2018
Structure and reactivity/selectivity control by oriented-external electric fields journal January 2018
Oriented internal electrostatic fields: an emerging design element in coordination chemistry and catalysis journal January 2022
Directing effects in inorganic substitution reactions. Part I. A hypothesis to explain the trans-effect journal January 1955
Electrostatic Origin of the Catalytic Power of Enzymes and the Role of Preorganized Active Sites journal October 1998