Publication | Closed Access
Defining Single Molecular Forces Required to Activate Integrin and Notch Signaling
567
Citations
31
References
2013
Year
Cell AdhesionMolecular BiologyCytoskeletonCellular PhysiologyMembrane ReceptorsSignaling PathwayMatrix BiologyCell SignalingBiophysicsNotch ReceptorsBiomolecular InteractionCell BiomechanicsNotch SignalingCell BiologySignal TransductionNatural SciencesCell-matrix InteractionCell MotilityTension Gauge TetherMolecular BiophysicsCellular BiochemistryActivate IntegrinMedicineSingle Molecular ForcesExtracellular Matrix
Cell-cell and cell-matrix mechanical interactions through membrane receptors direct a wide range of cellular functions and orchestrate the development of multicellular organisms. To define the single molecular forces required to activate signaling through a ligand-receptor bond, we developed the tension gauge tether (TGT) approach in which the ligand is immobilized to a surface through a rupturable tether before receptor engagement. TGT serves as an autonomous gauge to restrict the receptor-ligand tension. Using a range of tethers with tunable tension tolerances, we show that cells apply a universal peak tension of about 40 piconewtons (pN) to single integrin-ligand bonds during initial adhesion. We find that less than 12 pN is required to activate Notch receptors. TGT can also provide a defined molecular mechanical cue to regulate cellular functions.
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