posted on 2017-03-17, 00:00authored byYi-Ran Liang, Li-Na Zhu, Jie Gao, Hong-Xia Zhao, Ying Zhu, Sheng Ye, Qun Fang
Here we describe the combination
of three-dimensional (3D) printed chip and automated microfluidic
droplet-based screening techniques for achieving massively parallel,
nanoliter-scale protein crystallization screening under vapor diffusion
mode. We fabricated high-density microwell array chips for sitting-drop
vapor diffusion crystallization utilizing the advantage of the 3D-printing
technique in producing high-aspect-ratio chips. To overcome the obstacle
of 3D-printed microchips in performing long-term reactions caused
by their porousness and gas permeability properties in chip body,
we developed a two-step postprocessing method, including paraffin
filling and parylene coating, to achieve high sealability and stability.
We also developed a simple method especially suitable for controlling
the vapor diffusion speed of nanoliter-scale droplets by changing
the layer thickness of covering oil. With the above methods, 84 tests
of nanoliter-scale protein crystallization under vapor diffusion mode
were successfully achieved in the 7 × 12 droplet array chip with
a protein consumption of 10 nL for each test, which is 20–100
times lower than that in the conventional large-volume screening system.
Such a nanoliter-scale vapor diffusion system was applied to two model
proteins with commercial precipitants and displayed advantages over
that under microbatch mode. It identified more crystallization conditions,
especially for the protein samples with lower concentrations.