Institute of Biology, Center for Structural and Cell Biology in Medicine, University of Lübeck , Ratzeburger Allee 160, 23562 Lübeck, Germany.
Institute of Biochemistry, Center for Structural and Cell Biology in Medicine, University of Lübeck , Ratzeburger Allee 160, 23562 Lübeck, Germany.
Struct Dyn. 2015 May 22;2(4):041712. doi: 10.1063/1.4921591. eCollection 2015 Jul.
X-ray crystallography requires sufficiently large crystals to obtain structural insights at atomic resolution, routinely obtained in vitro by time-consuming screening. Recently, successful data collection was reported from protein microcrystals grown within living cells using highly brilliant free-electron laser and third-generation synchrotron radiation. Here, we analyzed in vivo crystal growth of firefly luciferase and Green Fluorescent Protein-tagged reovirus μNS by live-cell imaging, showing that dimensions of living cells did not limit crystal size. The crystallization process is highly dynamic and occurs in different cellular compartments. In vivo protein crystallization offers exciting new possibilities for proteins that do not form crystals in vitro.
X 射线晶体学需要足够大的晶体才能在原子分辨率下获得结构洞察力,这通常是通过耗时的体外筛选来实现的。最近,人们成功地使用高亮度自由电子激光和第三代同步加速器辐射从活细胞内生长的蛋白质微晶体中收集到了数据。在这里,我们通过活细胞成像分析了萤火虫荧光素酶和 GFP 标记的呼肠孤病毒 μNS 的体内晶体生长情况,结果表明活细胞的大小并不限制晶体的大小。结晶过程是高度动态的,发生在不同的细胞区室中。体内蛋白质结晶为那些在体外不能形成晶体的蛋白质提供了令人兴奋的新可能性。