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Biology subjects

Charbonnier, T.

Publications and source records attributed to Charbonnier, T..

2 recordsLinked to original sources

βII and βIII spectrin paralogues define robustness and specialization of the neuronal membrane periodic skeleton

Neuron connectivity and signal processing rely on a complex, dynamic morphology regulated by the cytoskeleton. The membrane-associated periodic skeleton (MPS), a 190-nm periodic actin-spectrin lattice, is a conserved feature of neurons. Here, we show that the dendritic MPS is built from a dual {beta}-spectrin system in which {beta}II- and {beta}III-spectrins are co-expressed and interleaved at the nanoscale in shafts and spine necks. 3D MINFLUX nanoscopy suggests that these paralogues form both homotypic ({beta}II- or {beta}III-only) and heterotypic ({beta}II/{beta}III) tetramers with an approximately 100-nm radial periodicity. Either paralogue alone is sufficient to maintain lattice architecture, whereas their combined loss disrupts MPS integrity. Using targeted mutagenesis, we show that actin binding is required to stabilize both paralogues within the MPS, whereas {beta}III-spectrin additionally depends on phosphoinositide interactions. Our findings reveal that, unlike the axonal MPS, the dendritic MPS is a composite scaffold in which structural redundancy coexists with paralogue-specific regulatory mechanisms, with potential consequences for synaptic function.

neuroscience↗

Biomimetic, smart and multivalent ligands for G-quadruplex isolation and bioorthogonal imaging

G-quadruplexes (G4s) continue to gather wide attention in the field of chemical biology as their prevalence in the human genome and transcriptome strongly suggests that they may play key regulatory roles in cell biology. G4-specific, cell-permeable small molecules (G4-ligands) innovately permit the interrogation of cellular circuitries in order to assess to what extent G4s influence cell fate and functions. Here, we report on multivalent, biomimetic G4-ligands referred to as TASQs that enable both the isolation and visualization of G4s in human cells. Two biotinylated TASQs, BioTASQ and BioCyTASQ, are indeed efficient molecular tools to fish out G4s of mixtures of nucleic acids through simple affinity capture protocols and to image G4s in cells via a biotin/avidin pretargeted imaging system first applied here to G4s, found to be a reliable alternative to in situ click chemistry. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=109 SRC="FIGDIR/small/422878v1_ufig1.gif" ALT="Figure 1"> View larger version (42K): org.highwire.dtl.DTLVardef@2db02dorg.highwire.dtl.DTLVardef@1897e59org.highwire.dtl.DTLVardef@1c63716org.highwire.dtl.DTLVardef@4a8a5d_HPS_FORMAT_FIGEXP M_FIG C_FIG

biophysics↗