Sergi Garcia-Manyes, Single Molecule Mechanobiology laboratory, The Francis Crick Institute and King\u2019s College London<\/em><\/p>\n <\/p>\n Cellular mechanostransduction relies on the conversion of mechanical cues into chemical signals, which propagate from the focal adhesion hub through the cytoskeleton to ultimately reach the nucleus through the Nuclear Pore Complex (NPC), and switch on specific force-dependent transcriptional programmes. However, how cellular mechanotransduction is regulated by the nanomechanical properties of the underpinning force-bearing proteins remains largely unknown. Here we first used a newly developed single-molecule magnetic tweezers combined with UV-light to demonstrate that oxidation of a previously cryptic methionine in the talin mechanosensor impairs vinculin binding. When translating the single-molecule findings into the cellular context, we found a loss in talin\/vinculin co-localisation at focal adhesions of NIH3T3 mouse fibroblasts when exposed to \u00b5M concentrations of H2<\/sub>O2<\/sub> and a decrease in the nuclear localisation of the YAP transcription factor (TF). In this vein, how the nuclear shuttling of mechanosensitive TFs is regulated by their mechanical properties remains also unclear. \u00a0By using a combination of single-molecule mechanics and single-cell optogenetics, we discovered that proteins with locally soft regions in the vicinity of the\u00a0nuclear-localization\u00a0sequence exhibit higher\u00a0nuclear-import rates. Inspired by these findings, we designed a\u00a0short and easy-to-express\u00a0unstructured\u00a0peptide tag that accelerates the nuclear-import rate of\u00a0stiff protein cargos. Altogether, our cross-scale experiments provide a single molecule perspective onto cellular mechanotransduction.<\/p>\n <\/p>\n <\/p>\n","protected":false},"excerpt":{"rendered":"