1,301 research outputs found

    Optimal State Transfer and Entanglement Generation in Power-law Interacting Systems

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    We present an optimal protocol for encoding an unknown qubit state into a multiqubit Greenberger-Horne-Zeilinger-like state and, consequently, transferring quantum information in large systems exhibiting power-law (1/rα1/r^\alpha) interactions. For all power-law exponents α\alpha between dd and 2d+12d+1, where dd is the dimension of the system, the protocol yields a polynomial speedup for α>2d\alpha>2d and a superpolynomial speedup for α≤2d\alpha\leq 2d, compared to the state of the art. For all α>d\alpha>d, the protocol saturates the Lieb-Robinson bounds (up to subpolynomial corrections), thereby establishing the optimality of the protocol and the tightness of the bounds in this regime. The protocol has a wide range of applications, including in quantum sensing, quantum computing, and preparation of topologically ordered states. In addition, the protocol provides a lower bound on the gate count in digital simulations of power-law interacting systems.Comment: Updated Table I, Additional discussion on a lower bound for the gate count in digital quantum simulatio

    Automated electrophysiological and pharmacological evaluation of human pluripotent stem cell-derived cardiomyocytes

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    Automated planar patch clamp systems are widely used in drug evaluation studies because of their ability to provide accurate, reliable, and reproducible data in a high-throughput manner. Typically, CHO and HEK tumorigenic cell lines overexpressing single ion channels are used since they can be harvested as high-density, homogenous, single-cell suspensions. While human pluripotent stem cell-derived cardiomyocytes (hPSC-CMs) are physiologically more relevant, these cells are fragile, have complex culture requirements, are inherently heterogeneous, and are expensive to produce, which has restricted their use on automated patch clamp (APC) devices. Here, we used high efficiency differentiation protocols to produce cardiomyocytes from six different hPSC lines for analysis on the Patchliner (Nanion Technologies GmbH) APC platform. We developed a two-step cell preparation protocol that yielded cell catch rates and whole-cell breakthroughs of ∼80%, with ∼40% of these cells allowing electrical activity to be recorded. The protocol permitted formation of long-lasting (>15 min), high quality seals (>2 GΩ) in both voltage- and current-clamp modes. This enabled density of sodium, calcium, and potassium currents to be evaluated, along with dose–response curves to their respective channel inhibitors, tetrodotoxin, nifedipine, and E-4031. Thus, we show the feasibility of using the Patchliner platform for automated evaluation of the electrophysiology and pharmacology of hPSC-CMs, which will enable considerable increase in throughput for reliable and efficient drug evaluation
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