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鞭毛蛋白F41片段的结晶及从极薄晶体中收集数据。

Crystallization of the F41 fragment of flagellin and data collection from extremely thin crystals.

作者信息

Samatey F A, Imada K, Vonderviszt F, Shirakihara Y, Namba K

机构信息

Protonic NanoMachine Project, ERATO, JST, 3-4 Hikaridai, Seika 619-0237, Japan.

出版信息

J Struct Biol. 2000 Nov;132(2):106-11. doi: 10.1006/jsbi.2000.4312.

Abstract

Flagellin, which constructs supercoiled filaments of the bacterial flagellum, is very difficult to crystallize because of its strong tendency to polymerize. We therefore crystallized the F41 fragment of flagellin, which does not polymerize because terminal regions that play important roles in polymerization are cleaved off. F41 was crystallized by the hanging drop vapor diffusion method in a mixture of polyethylene glycol, glycerol, and isopropanol, with a reservoir solution covered with silicon oil. The two key factors for success in growing sufficiently large crystals were isopropanol and silicon oil, which worked well to reduce the otherwise very high nucleation rate that resulted in hundreds of tiny crystals. The crystals were grown to very thin plates with thickness less than 10 microm, which made the collection of diffraction data very difficult. Freezing and annealing of the crystals and irradiation at synchrotron beamlines had to be carried out by specific methods and under specific conditions for its structure analysis at 2.0-A resolution.

摘要

鞭毛蛋白构成细菌鞭毛的超螺旋丝,由于其强烈的聚合倾向,很难结晶。因此,我们使鞭毛蛋白的F41片段结晶,该片段不会聚合,因为在聚合过程中起重要作用的末端区域被切除了。F41通过悬滴气相扩散法在聚乙二醇、甘油和异丙醇的混合物中结晶,储液用硅油覆盖。生长出足够大晶体的两个关键因素是异丙醇和硅油,它们能有效降低原本非常高的成核速率,否则会产生数百个微小晶体。晶体生长成厚度小于10微米的非常薄的薄片,这使得收集衍射数据非常困难。为了在2.0埃分辨率下进行结构分析,必须通过特定方法并在特定条件下对晶体进行冷冻、退火以及在同步加速器光束线进行照射。

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