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Dannersoe, J. K.

Publications and source records attributed to Dannersoe, J. K..

2 recordsLinked to original sources

Double Periodicity of the AnkyrinG-Associated Complex in the Axon Initial Segment

The axon initial segment (AIS), situated within the first 20-60 {micro}m of the axon, is essential for action potential generation and maintenance of axonal identity. Its structure relies on the beta ({beta})-IV-spectrin/AnkyrinG (AnkG) scaffold arranged periodically underneath the plasma membrane, harbouring diverse membrane proteins. Although a [~]190-nm cytoskeletal periodic organization is well established, the precise stoichiometry and spatial arrangement of AIS proteins within the [~]190-nm spatial period remain rudimentary, mostly for lack of sufficient spatial resolution and labelling efficiency. Here, using expansion microscopy and cryo-electron tomography, which overcome these technical limitations, we present data on the organization of the AnkG-associated complex within the [~]190-nm spatial period. We demonstrate that exactly two AnkG molecules with their C-termini separated by [~]80 nm are situated within each period. By contrast, the AnkG-associated cell-adhesion protein neurofascin-186 appears in clusters of varying sizes that are consistent with the periodic organisation of AnkG pairs, yet suggest a more complex molecular arrangement between the two molecules. Altogether, our novel approach provides new insights into AIS molecular organisation and protein stoichiometry.

neuroscience↗

Conserved N-terminal Regulation of the ACA8 Calcium Pump with Two Calmodulin Binding Sites

The autoinhibited plasma membrane calcium ATPase, ACA8 from A. thaliana has an N-terminal autoinhibitory domain. Calcium-bound calmodulin binding at two sites located at residues 42-62 and 74-96 relieves autoinhibition of ACA8 activity. We investigated N-terminally truncated ACA8 constructs (WT, {Delta}20, {Delta}30, {Delta}35, {Delta}37, {Delta}40, {Delta}74 and {Delta}100) to explore the role of conserved motifs in the N-terminal segment preceding the calmodulin binding sites. Furthermore, we purified WT, {Delta}20- and {Delta}100-ACA8, tested activity in vitro and performed structural studies of purified {Delta}20-ACA8 stabilized in its native form to explore the mechanism of autoinhibition. Through activity studies and a yeast complementation assay, we show that an N-terminal segment between residues 20 and 35, upstream of the calmodulin binding sites, is important for autoinhibition and the activation by calmodulin, and that a conserved Phe32 is essential for autoinhibition. Cryo-EM structure determination at 3.3 [A] resolution of a beryllium fluoride inhibited form shows no autoinhibition, but a low-resolution structure for an E1 state indicates autoinhibitory domain binding consistent with the mutational studies and AlphaFold predicted structures.

biochemistry↗