Issue 6, 2011

2D-SEIRAspectroscopy to highlight conformational changes of the cytochrome coxidase induced by direct electron transfer

Abstract

Potentiometric titrations of the cytochrome c oxidase (CcO) immobilized in a biomimetic membrane system were followed by two-dimensional surface-enhanced IR absorption spectroscopy (2D SEIRAS) in the ATR-mode. Direct electron transfer was employed to vary the redox state of the enzyme. The CcO was shown to undergo a conformational transition from a non-activated to an activated state after it was allowed to turnover in the presence of oxygen. Differences between the non-activated and activated state were revealed by 2D SEIRA spectra recorded as a function of potential. The activated state was characterized by a higher number of correlated transitions as well as a higher number of amino acids associated with electron transfer.

Graphical abstract: 2D-SEIRA spectroscopy to highlight conformational changes of the cytochrome c oxidase induced by direct electron transfer

Supplementary files

Article information

Article type
Paper
Submitted
19 Nov 2010
Accepted
25 Mar 2011
First published
04 May 2011

Metallomics, 2011,3, 619-627

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