Selimović Seila, Jia Yanwei, Fraden Seth
Complex Fluids Group, Martin Fisher School of Physics, Brandeis University, Waltham, MA 02454.
Cryst Growth Des. 2009 Apr 1;9(4):1806-1810. doi: 10.1021/cg800990k.
We employ the PhaseChip, a (poly)dimethylsiloxane (PDMS) microfluidic device, for statistical studies of protein crystal nucleation. The PhaseChip is designed to decouple nucleation and growth of protein crystals and so improve their yield and quality. Two layers of fluidic channels containing salt reservoirs and nanoliter-sized wells for protein drops in oil are separated by a thin PDMS membrane, which is permeable to water, but not to salt or macromolecules such as protein. We reversibly vary the supersaturation of protein inside the stored droplets by controlling the chemical potential of the reservoir. Lysozyme in the presence of sodium chloride is used as a model system. We determine the crystal nucleation rate as a function of protein supersaturation by counting the number of crystal nuclei per droplet, as demonstrated by Galkin and Vekilov.1.
我们使用PhaseChip,一种(聚)二甲基硅氧烷(PDMS)微流控装置,用于蛋白质晶体成核的统计研究。PhaseChip旨在使蛋白质晶体的成核和生长解耦,从而提高其产量和质量。两层包含盐储器和用于油中蛋白质液滴的纳升大小孔的流体通道由一层薄的PDMS膜隔开,该膜对水可渗透,但对盐或蛋白质等大分子不可渗透。我们通过控制储器的化学势来可逆地改变储存液滴内蛋白质的过饱和度。以氯化钠存在下的溶菌酶作为模型系统。如Galkin和Vekilov所证明的,我们通过计算每个液滴中的晶核数量来确定晶体成核速率作为蛋白质过饱和度的函数。1.