Harrison Reid R, Kolb Ilya, Kodandaramaiah Suhasa B, Chubykin Alexander A, Yang Aimei, Bear Mark F, Boyden Edward S, Forest Craig R
Intan Technologies, Los Angeles, California;
Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology, Atlanta, Georgia;
J Neurophysiol. 2015 Feb 15;113(4):1275-82. doi: 10.1152/jn.00629.2014. Epub 2014 Nov 26.
Patch clamping is a gold-standard electrophysiology technique that has the temporal resolution and signal-to-noise ratio capable of reporting single ion channel currents, as well as electrical activity of excitable single cells. Despite its usefulness and decades of development, the amplifiers required for patch clamping are expensive and bulky. This has limited the scalability and throughput of patch clamping for single-ion channel and single-cell analyses. In this work, we have developed a custom patch-clamp amplifier microchip that can be fabricated using standard commercial silicon processes capable of performing both voltage- and current-clamp measurements. A key innovation is the use of nonlinear feedback elements in the voltage-clamp amplifier circuit to convert measured currents into logarithmically encoded voltages, thereby eliminating the need for large high-valued resistors, a factor that has limited previous attempts at integration. Benchtop characterization of the chip shows low levels of current noise [1.1 pA root mean square (rms) over 5 kHz] during voltage-clamp measurements and low levels of voltage noise (8.2 μV rms over 10 kHz) during current-clamp measurements. We demonstrate the ability of the chip to perform both current- and voltage-clamp measurement in vitro in HEK293FT cells and cultured neurons. We also demonstrate its ability to perform in vivo recordings as part of a robotic patch-clamping system. The performance of the patch-clamp amplifier microchip compares favorably with much larger commercial instrumentation, enabling benchtop commoditization, miniaturization, and scalable patch-clamp instrumentation.
膜片钳技术是一种金标准的电生理技术,它具有时间分辨率和信噪比,能够记录单离子通道电流以及可兴奋单细胞的电活动。尽管其有用性且经过了数十年的发展,但膜片钳所需的放大器昂贵且体积庞大。这限制了用于单离子通道和单细胞分析的膜片钳技术的可扩展性和通量。在这项工作中,我们开发了一种定制的膜片钳放大器微芯片,该芯片可以使用标准的商业硅工艺制造,能够进行电压钳和电流钳测量。一项关键创新是在电压钳放大器电路中使用非线性反馈元件,将测量到的电流转换为对数编码电压,从而无需使用大型高值电阻,而这一因素限制了以往的集成尝试。芯片的台式表征显示,在电压钳测量期间电流噪声水平较低[5 kHz范围内均方根(rms)为1.1 pA],在电流钳测量期间电压噪声水平较低(10 kHz范围内rms为8.2 μV)。我们展示了该芯片在体外对HEK293FT细胞和培养神经元进行电流钳和电压钳测量的能力。我们还展示了其作为机器人膜片钳系统的一部分进行体内记录的能力。该膜片钳放大器微芯片的性能与大得多的商业仪器相比具有优势,可实现台式仪器的商品化、小型化和可扩展的膜片钳仪器。