Key result
Multiparametric atomic force microscopy revealed nanoscale mechanical heterogeneities on the Trypanosoma brucei cell surface, with alternating regions of softer (~50 kPa) and stiffer (~100 kPa) elasticity.
Multiparametric atomic force microscopy reveals nanoscale mechanical heterogeneities on the surface of Trypanosoma brucei, offering insights for designing trypanocidal drugs.
May guide trypanocidal drug design targeting surface mechanics; leaves open therapeutic exploitation pending validation.
A unique feature of the African trypanosome Trypanosoma brucei is the presence of an outer layer made of densely packed variable surface glycoproteins (VSGs), which enables the cells to survive in the bloodstream. Although the VSG coat is critical to pathogenesis, how exactly the glycoproteins are organized at the nanoscale is poorly understood. Here, we show that multiparametric atomic force microscopy is a powerful nanoimaging tool for the structural and mechanical characterization of trypanosomes, in a label-free manner and in buffer solution. Directly correlated images of the structure and elasticity of trypanosomes enable us to identify multiple nanoscale mechanical heterogeneities on the cell surface. On a ∼250 nm scale, regions of softer (Young’s modulus ∼50 kPa) and stiffer (∼100 kPa) elasticity alternate, revealing variations of the VSG coat and underlying structures. Our nanoimaging experiments show that the T. brucei cell surface is more heterogeneous than previously anticipated and offer promising prospects for the design of trypanocidal drugs targeting cell surface components.
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Valotteau et al. (2020) studied Trypanosoma brucei cell surface structure. Multiparametric atomic force microscopy was evaluated on Structural and mechanical characterization of trypanosomes. Multiparametric atomic force microscopy revealed nanoscale mechanical heterogeneities on the Trypanosoma brucei cell surface, with alternating regions of softer (~50 kPa) and stiffer (~100 kPa) elasticity.
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