Candoni Nadine, Grossier Romain, Hammadi Zoubida, Morin Roger, Veesler Stéphane
CNRS, Aix-Marseille University, CINaM (Centre Interdisciplnaire de Nanosciences de Marseille), Campus de Luminy, Case 913, F-13288 Marseille Cedex 09, France.
Protein Pept Lett. 2012 Jul;19(7):714-24. doi: 10.2174/092986612800793136.
The aim of this review is to provide biocrystallographers who intend to tackle protein-crystallization with theory and practical examples. Crystallization involves two separate processes, nucleation and growth, which are rarely completely unconnected. Here we give theoretical background and concrete examples illustrating protein crystallization. We describe the nucleation of a new phase, solid or liquid, and the growth and transformation of existing crystals obtained by primary or secondary nucleation or by seeding. Above all, we believe that a thorough knowledge of the phase diagram is vital to the selection of starting position and path for any crystallization experiment.
本综述的目的是为那些打算运用理论和实际例子来解决蛋白质结晶问题的生物晶体学家提供帮助。结晶涉及两个独立的过程,即成核和生长,这两个过程很少是完全不相关的。在这里,我们给出理论背景和具体例子来说明蛋白质结晶。我们描述了新相(固相或液相)的成核,以及通过一次或二次成核或接种获得的现有晶体的生长和转变。最重要的是,我们认为对相图有透彻的了解对于任何结晶实验起始位置和路径的选择至关重要。