Free interconversion of cytochrome C (CytC) between native ferrous (Cyt‐Fe II ) and oxidized ferric (CytC‐Fe III ) states is necessary to maintain the respiratory function of mitochondria. Disturbances in CytC‐Fe III to total CytC ratio may indicate mitochondrial dysfunction and apoptosis. Thus, tracking CytC oxidation state delivers important information about cellular physiology. In this work, we propose a novel methodology based on resonance Raman (rR) imaging optimized uniquely to track and qualitatively analyze the transition of Cyt‐Fe II to CytC‐Fe III within live cells without affecting their morphology. None of the commonly used excitation lines allows such clear‐cut differentiation, contrary to the 405 nm applied in this work. The presented methodology provides a novel pathway in the label‐free detection of ferrous and ferric heme proteins.
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Szczęsny-Małysiak et al. (2024) studied this question.
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