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Massam-Wu, T.

Publications and source records attributed to Massam-Wu, T..

5 recordsLinked to original sources

Solid-state NMR Reveals Mobility-Based Organisation of the Schizosaccharomyces pombe Cell Wall

Fungal cell walls are hierarchically organised polysaccharide networks whose mechanical and functional properties depend on both chemical composition and molecular organisation. Although glucan synthases are essential for cell wall biosynthesis, how individual synthases shape the supramolecular architecture and dynamics of intact walls remains poorly understood. Here, we combine mobility-resolved 13C solid-state NMR spectroscopy with targeted genetic perturbation of the glucan synthases Ags1, Bgs1, and Bgs4 to determine how synthase activity governs the molecular organisation of the Schizosaccharomyces pombe cell wall. We first establish a molecular level reference for the wild-type wall by identifying the major glucan and mannan environments and resolving polysaccharides according to their mobility directly in intact cells. The rigid wall scaffold is dominated by unbranched {beta}-1,3-glucan and -1,3-glucan, whereas branched glucans and mannans occupy more dynamic molecular environments. Comparison with thermosensitive glucan synthase mutants reveals distinct, mutation-dependent reorganisation of both the rigid structural scaffold and the mobile polysaccharide matrix. Quantitative analysis further shows that, despite retaining broadly similar glucan compositions, the Ags1, Bgs1, and Bgs4 mutants redistribute carbohydrates among rigid, intermediate, and mobile molecular environments in distinct ways. These mutation-specific mobility fingerprints demonstrate that glucan synthases regulate not only polysaccha-ride biosynthesis but also how cell wall polymers are assembled, packed, and dynamically organised within the intact wall. More broadly, our findings establish molecular mobility as a sensitive signature of cell wall architecture that reveals structural consequences of biosynthetic perturbation not apparent from composition alone. Mobility-resolved solid-state NMR therefore provides a powerful framework for linking genetic perturbations to molecular dynamics and supramolecular organisation in intact fungal cell walls.

biophysics↗

Tropomyosin and Vinculin antagonistically mediate GPI-anchored protein nanoclustering

The plasma membrane is laterally organised into dynamic nanoscale and mesoscale domains. Glycosylphosphatidylinositol-anchored proteins (GPI-APs) form actomyosin dependent nanoclusters at the outer leaflet of the plasma membrane via transbilayer coupling to inner leaflet lipids. These nanoclusters are nucleated downstream of integrin activation in a mechanochemical fashion and require vinculin and myosin 1 activity. Here, we identify an antagonistic relationship between vinculin and a negative regulator of myosin 1, tropomyosin, in regulating GPI-AP nanoclustering. We show vinculin mediated restoration of clustering is myosin-1 sensitive. The actin and lipid-binding vinculin tail is sufficient to restore clustering, indicating that vinculin, in particular its actin and lipid-proximal tail promote nanoclustering. Furthermore, re-expression of the non-muscle tropomyosin isoform Tpm2.1 in Tpm2-deficient MDA-MB-231 cells suppress GPI-AP nanoclustering while Tpm2.1 mutants defective in stable actin-filament association do not. Structural superposition of actin-bound vinculin tail and tropomyosin assemblies suggests that vinculin and tropomyosin engage overlapping or closely adjacent surfaces on actin filaments. Consistent with this, depletion of tropomyosin in vinculin-null cells restores GPI-AP nanoclustering. Together these results suggest that competitive interactions between tropomyosin and vinculin regulate actin availability for myosin 1 and hence contribute to the regulation of GPI-AP nanoclusters.

cell biology↗

StayRose: a photostable StayGold derivative red-shifted by genetic code expansion

Photobleaching of fluorescent proteins often limits the acquisition of high-quality images in microscopy. StayGold, a novel dimeric green fluorescent protein recently monomerised through sequence engineering, addresses this challenge with its high photostability. There is now focus on producing different colour StayGold derivatives to facilitate concurrent tagging of multiple targets. The unnatural amino acid 3-aminotyrosine has previously been shown to red-shift super folder GFP upon incorporation into its chromophore via genetic code expansion. Here we apply the same strategy to red-shift StayGold through substitution of Tyrosine-58 with 3-aminotyrosine. The resultant red fluorescent protein, StayRose, shows 530 nm excitation and 588 nm emission peaks, shifting from the 497 nm and 504 nm excitation and emission peaks of StayGold. StayRose also retains the favourable photostability of StayGold and can be similarly monomerised using mutations at the dimer interface. A high-resolution crystal structure of StayRose confirms the modified structure of the amino-chromophore within an unperturbed 3D fold. Although reliant on genetic code expansion, StayRose provides an important step towards developing red-shifted StayGold derivatives.

bioengineering↗

mNeonGreen-tagged fusion proteins and nanobodies reveal localization of tropomyosin to patches, cables, and contractile actomyosin rings in live yeast cells

Tropomyosins are structurally conserved -helical coiled-coil dimeric proteins that bind along the length of filamentous actin (F-actin) in fungi and animals. Tropomyosins play essential roles in the stability of actin filaments in non-muscle cells and are essential for calcium regulation of myosin II contractility in the muscle. Despite the crucial role of tropomyosin in actin cytoskeletal regulation, in vivo investigations of tropomyosin are limited, mainly due to the suboptimal live cell imaging tools currently available in many organisms. Here, we report mNeon-Green (mNG) tagged tropomyosin, with native promoter and linker length configuration, that clearly reports tropomyosin localization and dynamics in Schizosaccharomyces pombe (Cdc8), Schizosaccharomyces japonicus (Cdc8), and Saccharomyces cerevisiae (Tpm1 and Tpm2), in vivo and in isolated S. pombe cell division apparatuses. We extended this approach to also visualize the mammalian TPM2 isoform. Finally, we generated a camelid-nanobody against S. pombe Cdc8, which mimics the localization of mNG-Cdc8 in vivo without significantly influencing cell growth and dynamics of actin cytoskeleton. Using these tools, we report the presence of tropomyosin in previously unappreciated patch-like structures in fission and budding yeasts, show flow of tropomyosin (F-actin) cables to the cytokinetic actomyosin ring, and identify rearrangements of the actin cytoskeleton during mating. These powerful tools and strategies will aid better analyses of tropomyosin and actin cables in vivo.

cell biology↗

Defining endogenous TACC3-chTOG-clathrin-GTSE1 interactions at the mitotic spindle using induced relocalization

A multiprotein complex containing TACC3, clathrin, and other proteins has been implicated in mitotic spindle stability. To disrupt this complex in an anti-cancer context, we need to understand the composition of the complex and the interactions between complex members and with microtubules. Induced relocalization of proteins in cells is a powerful way to analyze protein-protein interactions and additionally monitoring where and when these interactions occur. We used CRISPR/Cas9 gene-editing to add tandem FKBP-GFP tags to each complex member. The relocalization of endogenous tagged protein from the mitotic spindle to mitochondria and assessment of the effect on other proteins allowed us to establish that TACC3 and clathrin are core complex members and that chTOG and GTSE1 are ancillary to the complex, respectively binding to TACC3 and clathrin, but not each other. PIK3C2A, a membrane trafficking protein that binds clathrin, was previously proposed to also bind TACC3 and stabilize the TACC3–chTOG–clathrin–GTSE1 complex during mitosis. We show that PIK3C2A is not on the mitotic spindle and that knockout of this gene had no effect on the localization of the complex. We therefore conclude that PIK3C2A is not a member of the TACC3–chTOG–clathrin–GTSE1 complex. This work establishes that targeting the TACC3–clathrin interface or their microtubule-binding sites are the two strategies most likely to disrupt spindle stability mediated by this multiprotein complex.Competing Interest StatementThe authors have declared no competing interest.View Full Text

cell biology↗