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Lipid Monolayer and Sparse Matrix Screening for Growing Two-Dimensional Crystals for Electron Crystallography: Methods and Examples

机译:用于生长电子晶体学的二维晶体的脂质单层和稀疏基质筛选:方法和实施例

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摘要

Electron microscopy provides an efficient method for rapidly assessing whether a solution of macromolecules is homogeneous and monodisperse. If the macromolecules can be induced to form two-dimensional crystals that are a single layer in thickness, then electron crystallography of frozen-hydrated crystals has the potential of achieving three-dimensional density maps at sub-nanometer or even atomic resolution. Here we describe the lipid monolayer and sparse matrix screening methods for growing two-dimensional crystals and present successful applications to soluble macromolecular complexes: carboxysome shell proteins and HIV CA, respectively. Since it is common to express recombinant proteins with poly-His tags for purification by metal affinity chromatography, the monolayer technique using bulk lipids doped with Ni2+ lipids has the potential for broad application. Likewise, the sparse matrix method uses screening conditions for three-dimensional crystallization and is therefore of broad applicability.
机译:电子显微镜为快速评估大分子溶液是否均匀和单分散提供了一种有效的方法。如果可以诱导大分子形成单层厚度的二维晶体,​​那么冷冻水合晶体的电子晶体学就有可能在亚纳米甚至原子分辨率下获得三维密度图。在这里,我们描述了用于生长二维晶体的脂质单层和稀疏基质筛选方法,并提出了对可溶性大分子复合物的成功应用:分别是羧化壳蛋白和HIVCA。由于通常表达带有多组氨酸标签的重组蛋白以通过金属亲和层析纯化,因此使用掺有Ni 2 + 脂质的块状脂质的单层技术具有广泛的应用潜力。同样,稀疏矩阵法使用筛选条件进行三维结晶,因此具有广泛的适用性。

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