4.8 Article

Real-time quantitative characterization of ion channel activities for automated control of a lipid bilayer system

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BIOSENSORS & BIOELECTRONICS
卷 237, 期 -, 页码 -

出版社

ELSEVIER ADVANCED TECHNOLOGY
DOI: 10.1016/j.bios.2023.115490

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Model cell membrane; Electrophysiology; Digital signal processing; MEMS devices; Biohybrid robotics; Laboratory automation

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This paper presents a novel signal processing method for real-time and quantitative characterization of ion channel activities on a lipid bilayer system. The characterization of ion channel activities has traditionally relied on time-consuming analyses after recording, posing a challenge in incorporating the system into practical applications. The proposed system divides the ion channel signal into short segments for processing during the recording, allowing for real-time characterization and response.
This paper describes a novel signal processing method to characterize the activity of ion channels on a lipid bilayer system in a real-time and quantitative manner. Lipid bilayer systems, which enable single-channel level recordings of ion channel activities against physiological stimuli in vitro, are gaining attention in various research fields. However, the characterization of ion channel activities has heavily relied on time-consuming analyses after recording, and the inability to return the quantitative results in real time has long been a bottleneck to incorporating the system into practical products. Herein, we report a lipid bilayer system that integrates realtime characterization of ion channel activities and real-time response based on the characterization result. Unlike conventional batch processing, an ion channel signal is divided into short segments and processed during the recording. After optimizing the system to maintain the same characterization accuracy as conventional operation, we demonstrated the usability of the system with two applications. One is quantitative control of a robot based on ion channel signals. The velocity of the robot was controlled every second, which was around tens of times faster than the conventional operation, in proportion to the stimulus intensity estimated from changes in ion channel activities. The other is the automation of data collection and characterization of ion channels. By constantly monitoring and maintaining the functionality of a lipid bilayer, our system enabled continuous recording of ion channels over 2 h without human intervention, and the time of manual labor has been reduced from conventional 3 h to 1 min at a minimum. We believe the accelerated characterization and response in the lipid bilayer systems presented in this work will facilitate the transformation of lipid bilayer technology toward a practical level, finally leading to its industrialization.

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