Cells transmit piconewton forces to receptors to mediate processes such as migration and immune recognition. Amajor challenge in quantifying such forces is the sparsity of cell mechanical events.A ccordingly,m olecular tension is typically quantified with high resolution fluorescence microscopy, which hinders widespread adoption and application. Here,w er eport am echanically triggered hybridization chain reaction (mechano-HCR) that allows chemicala mplification of mechanical events.The amplification is triggered when acell receptor mechanically denatures ad uplex revealing ac ryptic initiator to activate the HCR reaction in situ. Importantly, mechano-HCR enables direct readout of pN forces using ap late reader.W el everage this capability and measured mechano-IC 50 for aspirin, Y-27632, and eptifibatide.Given that cell mechanical phenotypes are of clinical importance,mechano-HCR may offer ac onvenient route for drug discovery, personalized medicine,and disease diagnosis.

Cardiac muscle cells (CMCs) are the unit cells that comprise the heart. CMCs go through different stages of differentiation and maturation pathways to fully mature into beating cells. These cells can sense and respond to mechanical cues through receptors such as integrins which influence maturation pathways. For example, cell traction forces are important for the differentiation and development of functional CMCs, as CMCs cultured on varying substrate stiffness function differently. Most work in this area has focused on understanding the role of bulk extracellular matrix stiffness in mediating the functional fate of CMCs. Given that stiffness sensing mechanisms are mediated by individual integrin receptors, an important question in this area pertains to the specific magnitude of integrin piconewton (pN) forces that can trigger CMC functional maturation. To address this knowledge gap, we used DNA adhesion tethers that rupture at specific thresholds of force (∼12, ∼56, and ∼160 pN) to test whether capping peak integrin tension to specific magnitudes affects CMC function. We show that adhesion tethers with greater force tolerance lead to functionally mature CMCs as determined by morphology, twitching frequency, transient calcium flux measurements, and protein expression (F-actin, vinculin, α-actinin, YAP, and SERCA2a). Additionally, sarcomeric actinin alignment and multinucleation were significantly enhanced as the mechanical tolerance of integrin tethers was increased. Taken together, the results show that CMCs harness defined pN integrin forces to influence early stage development. This study represents an important step toward biophysical characterization of the contribution of pN forces in early stage cardiac differentiation.

Hydrogels embedded with periodic arrays of nanoparticles display a striking photonic crystal coloration that may be useful for applications such as camouflage, anticounterfeiting, and chemical sensing. Dynamically generating color patterns requires control of nanoparticle organization within a polymer network on-demand, which is challenging. We solve this problem by creating a DNA hydrogel system that shows a 50 000-fold decrease in modulus upon heating by ∼10 °C. Magnetic nanoparticles entrapped within these DNA gels generate a structural color only when the gel is heated and a magnetic field is applied. A spatially controlled photonic crystal coloration was achieved by photopatterning with a near-infrared illumination. Color was “erased” by illuminating or heating the gel in the absence of an external magnetic field. The on-demand assembly technology demonstrated here may be beneficial for the development of a new generation of smart materials with potential applications in erasable lithography, encryption, and sensing.

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