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Abstract: G-protein coupled receptor (GPCRs) drug discovery is a thriving strategy in the pharmaceutical industry. The standard approach uses living cells to test millions of compounds in a high-throughput format. Typically, changes in the intracellular levels of key elements in the signaling cascade are monitored using fluorescence or luminescence read-out systems, which require external equipment for signal acquisition. In this work, thin-film amorphous silicon photodiodes with an integrated fluorescence filter were developed to capture the intracellular calcium dynamics in response to the activation of the endogenous muscarinic M1 GPCR of HEK 293T cells. Using the new device it was possible to characterize the potency of carbachol (EC50=10.5µM) and pirenzepine (IC50=4.2μM), with the same accuracy as standard microscopy optical systems. The smaller foot-print provided by the detection system makes it an ideal candidate for the future integration in microfluidic devices for drug discovery. [Copyright &y& Elsevier]

We report on the magnetization reversal mechanism of Co islands on Pt(111) as a function of their size and shape. We measure the zero-field susceptibility χ(T) and low-temperature magnetization curves M(H) with in situ magneto-optical Kerr effect. Together with the island morphology deduced from scanning tunneling microscopy, this creates sufficient information to determine both the magnetization reversal mechanism and the distribution of anisotropy energies between perimeter and surface atoms. We find a transition from quasicoherent rotation to domain wall nucleation and propagation with a critical size of 350 atoms for ramified, and of 600 atoms for compact islands. [ABSTRACT FROM AUTHOR]