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Demonstration of MEMS-based differential scanning calorimetry for determining thermodynamic properties of biomolecules

机译:演示基于MEMS的差示扫描量热法,用于确定生物分子的热力学性质

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摘要

We demonstrate microelectromechanical system (MEMS)-based differential scanning calorimetry (DSC) for characterizing thermodynamic properties of biomolecules. The MEMS device consists of a pair of polydimethylsiloxane (PDMS) calorimetric microchambers and fluid handling microchannels, with each chamber 1.2 μl in volume and based on a freestanding SU-8 diaphragm. A nickel-chromium thermopile, and nickel heaters and temperature sensors, are integrated on the diaphragms to allow thermal measurement and control. During DSC measurements, the chambers are filled with a biomolecular solution and reference buffer, respectively. As the solution temperatures are varied continuously over a range of interest, the biomolecular thermal power is measured via the thermopile output, and then used to compute the thermodynamic parameters of the biomolecule. We present results from applying the device to DSC measurements of the unfolding of the proteins lysozyme and ribonuclease A. The enthalpy of unfolding and melting temperature of the proteins obtained are in agreement with published data.
机译:我们演示了基于微机电系统(MEMS)的差示扫描量热法(DSC),用于表征生物分子的热力学性质。 MEMS装置由一对聚二甲基硅氧烷(PDMS)量热微腔室和流体处理微通道组成,每个腔室的体积为1.2μl,并基于独立式SU-8隔膜。隔膜上集成了镍铬热电堆,镍加热器和温度传感器,以进行热测量和控制。在DSC测量期间,分别将生物分子溶液和参考缓冲液填充到腔室中。当溶液温度在感兴趣的范围内连续变化时,通过热电堆输出来测量生物分子的热功率,然后将其用于计算生物分子的热力学参数。我们介绍了将设备应用于DSC测量溶菌酶和核糖核酸酶A的解折叠的结果。解折叠的焓和获得的蛋白的解链温度与公开数据一致。

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