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Real-time investigation of dynamic protein crystallization in living cellsa)

机译:活细胞动态蛋白质结晶的实时调查)

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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.
机译:X射线晶体学需要足够大的晶体来获得原子分辨率的结构见解,通过耗时的筛选常规地在体外获得。最近,使用高度辉煌的自由电子激光和第三代同步辐射辐射从活细胞内生长的蛋白质微晶来报告成功的数据收集。这里,通过活细胞成像,我们分析了萤火虫荧光素酶和绿色荧光蛋白标记的reovirusμns的体内晶体生长,表明活细胞的尺寸没有限制晶体尺寸。结晶过程是高度动态的并且发生在不同的细胞室中。在体内蛋白质结晶中,为不在体外形成晶体的蛋白质提供激动人心的新可能性。

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