Key result
Electron energy loss spectroscopy detects high neurofilament phosphorylation in squid giant axons and presynaptic terminals.
Electron energy loss spectroscopy can be used for high elemental and spatial resolution analysis of the phosphorylation state of cytoskeletal protein molecules in situ.
Enables high-resolution cytoskeletal analysis in model systems; leaves open translation to mammalian or human contexts.
We demonstrate that clusters of phosphorus atoms can be detected in energy loss spectroscopic images (ESI) of cytoskeletal proteins of squid axons. In series of images taken at four energy windows below and three windows above the phosphorus P-L2,3 ionization edge, signal-to-background intensity differences were analyzed by videodensitometry. A distinct increase of relative intensities was recorded above the phosphorus edge in neurofilaments of the peripheral giant axon and in those of the presynaptic terminal. A high level of neurofilament phosphorylation in the peripheral axon supports previous biochemical and immunochemical results, but our finding of phosphorylated neurofilaments in the presynaptic axon conflicts with these studies. Our method may be advantageous for analysis with high elemental and spatial resolution of the phosphorylation state of cytoskeletal protein molecules in situ.
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Martinꝉ et al. (1993) studied Protein phosphorylation in squid axons. Electron energy loss spectroscopy was evaluated on Detection of clusters of phosphorus atoms in cytoskeletal proteins. Electron energy loss spectroscopy detected high levels of neurofilament phosphorylation in both the peripheral giant axon and the presynaptic terminal of squid axons.
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