Microfluidic device for super-fast evaluation of membrane protein nanoparticle formation
Abstract
Membrane proteins embedded in bilayer lipids of cell membrane have unique functions including inter-cell communication and ionic/molecular transport. To understand the structure and function of the membrane protein embedded in a native biological bilayer lipid environment is a major research area in biology. A reconstitution/crystallisation process of membrane proteins and lipids can form virus-like nanoparticles, and have important potential applications in drug design and drug delivery. Earlier studies used a standard dialysis process that is inherently low-throughput, time consuming (days to weeks) and costly in protein materials. In this reported work a new microfluidic device is demonstrated to rapidly form membrane protein lipid nanoparticles in an extremely short period (seconds). The reconstitution process occurs using a continuous flow dominated by convection-diffusion phenomena in the microfluidic channel, which can form protein/lipid nanoparticles using only nanolitres or picolitres of protein sample. Moreover, a controllable syringe pump is used to test a combination of conditions, rather than using inefficient hand pipetting. Therefore this novel microfluidic device has an ability to rapidly form uniform membrane protein/lipid nanoparticles, and the authors believe that this new method will make a transformative impact on commercial applications in a variety of areas from biology to pharmacology.
Additional Information
© 2013 The Institution of Engineering and Technology. Published in Micro & Nano Letters; Received on 25th April 2013; Revised on 8th July 2013; Accepted on 17th July 2013. This work was supported by the Howard Hughes Medical Institute (HHMI). The authors thank their colleagues in the Departments of Mechanical Engineering, and Molecular, Cellular and Developmental Biology (MCDB) of the University of Colorado at Boulder, and the California Institute of Technology at Pasadena for helpful support and comments.Additional details
- Eprint ID
- 45473
- DOI
- 10.1049/mnl.2013.0216
- Resolver ID
- CaltechAUTHORS:20140505-081924948
- Howard Hughes Medical Institute (HHMI)
- Created
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2014-05-05Created from EPrint's datestamp field
- Updated
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2021-11-10Created from EPrint's last_modified field