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Protein Crystallization: Specific Phenomena and General Insights on Crystallization Kinetics

机译:蛋白质结晶:结晶动力学的特定现象和一般见解

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Experimental and simulation studies of the nucleation and growth kinetics of proteins have revealed phenomena that are specific for macromolecular crystallization, and others that provide a more detailed understanding of solution crystallization in general. The more specific phenomena, which include metastable liquid-liquid phase separations and gelation prior to solid nucleation, are due to the small ratio of the intermolecular interaction-range to the size of molecules involved. The apparently more generally applicable mechanisms include the cascade-like formation of macrosteps, as an intrinsic morphological instability that roots in the coupled bulk transport and nonlinear interface kinetics in systems with mixed growth rate control. Analyses of this nonlinear response provide (a) criteria for the choice of bulk transport conditions to minimize structural defect formation, and (b) indications that the "slow" protein crystallization kinetics stems from the mutual retardation of growth steps.
机译:蛋白质核细胞和生长动力学的实验性和仿真研究表明了大分子结晶特异性的现象,以及其他详细了解溶液结晶的其他方法。更具体的现象,包括亚稳态液 - 液相分离和在固体成核之前的凝胶化,是由于分子间相互作用范围与所涉及的分子尺寸的比例小。显然更普遍适用的机制包括甲丙的级联形成,作为具有混合生长速率控制的系统中耦合的散装输送和非线性界面动力学的内在形态不稳定。该非线性响应的分析提供(a)用于选择散装传输条件的标准,以最大限度地减少结构缺陷形成,(b)指示“慢”蛋白结晶动力学源于生长步骤的互延迟。

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