Department of Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, 600 S Mathews Ave, Urbana, IL, USA.
Lab Chip. 2018 Mar 13;18(6):944-954. doi: 10.1039/c7lc01141e.
Crystallization of membrane proteins is a critical step for uncovering atomic resolution 3-D structures and elucidating structure-function relationships. Microseeding, the process of transferring sub-microscopic crystal nuclei from initial screens into new crystallization experiments, is an effective, yet underutilized approach to grow crystals suitable for X-ray crystallography. Here, we report simplified methods for crystallization of membrane proteins that utilize microseeding in X-ray transparent microfluidic chips. First, a microfluidic method for introduction of microseed dilutions into metastable crystallization experiments is demonstrated for photoactive yellow protein and cytochrome bo oxidase. As microseed concentration decreased, the number of crystals decreased while the average size increased. Second, we demonstrate a microfluidic chip for microseed screening, where many crystallization conditions were formulated on-chip prior to mixing with microseeds. Crystallization composition, crystal size, and diffraction data were collected and mapped on phase diagrams, which revealed that crystals of similar diffraction quality and size typically grow in distinct regions of the phase diagram.
膜蛋白结晶是揭示原子分辨率三维结构和阐明结构-功能关系的关键步骤。晶种转移,即将亚微观晶核从初始筛选转移到新的结晶实验中的过程,是一种有效但未充分利用的方法,可用于生长适合 X 射线晶体学的晶体。在这里,我们报告了利用 X 射线透明微流控芯片中的晶种转移来结晶膜蛋白的简化方法。首先,我们展示了一种将微种稀释液引入亚稳结晶实验的微流控方法,用于光活性黄色蛋白和细胞色素 bo 氧化酶。随着微种浓度的降低,晶体数量减少,而平均尺寸增加。其次,我们展示了一种用于晶种筛选的微流控芯片,其中许多结晶条件在与晶种混合之前就在芯片上形成。收集并在相图上绘制了结晶成分、晶体尺寸和衍射数据,这表明具有相似衍射质量和尺寸的晶体通常在相图的不同区域生长。