| Literature DB >> 26478486 |
Doros T Petasis1, Michael P Hendrich2.
Abstract
Electron paramagnetic resonance (EPR) spectroscopy has long been a primary method for characterization of paramagnetic centers in materials and biological complexes. Transition metals in biological complexes have valence d-orbitals that largely define the chemistry of the metal centers. EPR spectra are distinctive for metal type, oxidation state, protein environment, substrates, and inhibitors. The study of many metal centers in proteins, enzymes, and biomimetic complexes has led to the development of a systematic methodology for quantitative interpretation of EPR spectra from a wide array of metal containing complexes. The methodology is now contained in the computer program SpinCount. SpinCount allows simulation of EPR spectra from any sample containing multiple species composed of one or two metals in any spin state. The simulations are quantitative, thus allowing determination of all species concentrations in a sample directly from spectra. This chapter will focus on applications to transition metals in biological systems using EPR spectra from multiple microwave frequencies and modes.Entities:
Keywords: EPR; Metalloenzymes; Metalloproteins; Multifrequency; Parallel-mode; Quantitative; Simulation; SpinCount; Transition metals
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Year: 2015 PMID: 26478486 PMCID: PMC5286561 DOI: 10.1016/bs.mie.2015.06.025
Source DB: PubMed Journal: Methods Enzymol ISSN: 0076-6879 Impact factor: 1.600