Shim Jung-Uk, Cristobal Galder, Link Darren R, Thorsen Todd, Fraden Seth
Complex Fluids Group, Martin Fisher School of Physics, Brandeis University, Waltham, MA 02454, USA.
Cryst Growth Des. 2007;7(11):2192-2194. doi: 10.1021/cg700688f.
A high throughput, low volume microfluidic device has been designed to decouple the physical processes of protein crystal nucleation and growth. This device, called the Phase Chip, is constructed out of poly(dimethylsiloxane) (PDMS) elastomer. One of the Phase Chip's innovations is to exploit surface tension forces to guide each drop to a storage chamber. We demonstrate that nanoliter water-in-oil drops of protein solutions can be rapidly stored in individual wells thereby allowing the screening of 1000 conditions while consuming a total of only 10 mug protein on a 20 cm(2) chip. Another significant advance over current microfluidic devices is that each well is in contact with a reservoir via a dialysis membrane through which only water and other low molecular weight organic solvents can pass, but not salt, polymer, or protein. This enables the concentration of all solutes in a solution to be reversibly, rapidly, and precisely varied in contrast to current methods, such as the free interface diffusion or sitting drop methods, which are irreversible. The Phase Chip operates by first optimizing conditions for nucleation by using dialysis to supersaturate the protein solution, which leads to nucleation of many small crystals. Next, conditions are optimized for crystal growth by using dialysis to reduce the protein and precipitant concentrations, which leads small crystals to dissolve while simultaneously causing only the largest ones to grow, ultimately resulting in the transformation of many small, unusable crystals into a few large ones.
一种高通量、低体积的微流控装置被设计用于将蛋白质晶体成核和生长的物理过程解耦。这种装置称为相芯片,由聚二甲基硅氧烷(PDMS)弹性体制成。相芯片的创新之一是利用表面张力将每个液滴引导至储存室。我们证明,蛋白质溶液的纳升级油包水液滴可快速储存在各个孔中,从而在一块20平方厘米的芯片上仅消耗总共10微克蛋白质的情况下就能筛选1000种条件。与当前的微流控装置相比,另一个显著进步是每个孔通过透析膜与储液器接触,只有水和其他低分子量有机溶剂可以通过透析膜,而盐、聚合物或蛋白质则不能。这使得溶液中所有溶质的浓度能够可逆、快速且精确地变化,这与诸如自由界面扩散或坐滴法等当前不可逆的方法形成对比。相芯片的操作过程是,首先通过透析使蛋白质溶液过饱和来优化成核条件,这会导致许多小晶体的成核。接下来,通过透析降低蛋白质和沉淀剂浓度来优化晶体生长条件,这会使小晶体溶解,同时仅使最大的晶体生长,最终导致许多小的、不可用的晶体转变为少数大晶体。