Nollert Peter
deCODE Genetics, BioStructures Group, 7869 NE Day Rd West, Bainbridge Island, WA 98110, USA.
J Appl Crystallogr. 2003 Oct;36(5):1295-1296. doi: 10.1107/S0021889803013724.
The use of lipidic cubic phases as crystal nucleation and growth matrices is becoming popular and has yielded crystals of soluble and membrane proteins. So far, all of the membrane proteins crystallized by this method have been colored. This feature has facilitated the detection of the often encountered microcrystals in initial screening rounds. Indeed, small colorless protein crystals have poor optical contrast as a result of the small differences in refractive index of the protein crystal and the surrounding lipidic cubic phase. While a perfect preparation of a lipidic cubic phase is transparent and optically isotropic, in a crystallization setup it frequently disguises crystals due to cracks, inclusions, surface distortions and phase boundaries. Here, several specialized microscopic techniques and illumination conditions are compared and it is found that sufficient contrast is generated by cross polarization microscopy and by Hoffman modulation contrast microscopy for the detection of colorless protein crystals.
使用脂质立方相作为晶体成核和生长基质正变得越来越普遍,并已获得了可溶性蛋白和膜蛋白的晶体。到目前为止,通过这种方法结晶的所有膜蛋白都是有颜色的。这一特性有助于在初始筛选轮次中检测经常遇到的微晶。实际上,由于蛋白质晶体与周围脂质立方相的折射率差异较小,无色小蛋白质晶体的光学对比度较差。虽然完美制备的脂质立方相是透明且光学各向同性的,但在结晶装置中,由于裂缝、内含物、表面畸变和相界,它常常会掩盖晶体。在这里,对几种专门的显微镜技术和照明条件进行了比较,发现交叉偏振显微镜和霍夫曼调制对比度显微镜能够产生足够的对比度来检测无色蛋白质晶体。