Garavito R M, Picot D, Loll P J
Department of Biochemistry and Molecular Biology, University Chicago, Illinois 60637, USA.
J Bioenerg Biomembr. 1996 Feb;28(1):13-27.
Crystallizing membrane proteins remains a challenging endeavor despite the increasing number of membrane protein structures solved by X-ray crystallography. The critical factors in determining the success of the crystallization experiments are the purification and preparation of membrane protein samples. Moreover, there is the added complication that the crystallization conditions must be optimized for use in the presence of detergents although the methods used to crystallize most membrane proteins are, in essence, straightforward applications of standard methodologies for soluble protein crystallization. The roles that detergents play in stability and aggregation of membrane proteins as well as the colloidal properties of the protein-detergent complexes need to be appreciated and controlled before and during the crystallization trials. All X-ray quality crystals of membrane proteins were grown from preparations of detergent-solubilized protein, where the heterogeneous natural lipids from the membrane have been replaced by a homogeneous detergent environment. It is the preparation of such monodisperse, isotropic solutions of membrane proteins that has allowed the successful application of the standard crystallization methods routinely used on soluble proteins. In this review, the issues of protein purification and sample preparation are addressed as well as the new refinements in crystallization methodologies for membrane proteins. How the physical behavior of the detergent, in the form of micelles or protein-detergent aggregates, affects crystallization and the adaptation of published protocols to new membrane protein systems are also addressed. The general conclusion is that many integral membrane proteins could be crystallized if pure and monodisperse preparations in a suitable detergent system can be prepared.
尽管通过X射线晶体学解析出的膜蛋白结构数量不断增加,但使膜蛋白结晶仍然是一项具有挑战性的工作。决定结晶实验成功与否的关键因素是膜蛋白样品的纯化和制备。此外,还有一个额外的复杂情况,即尽管用于结晶大多数膜蛋白的方法本质上是可溶性蛋白结晶标准方法的直接应用,但结晶条件必须针对在洗涤剂存在的情况下使用进行优化。在结晶试验之前和期间,需要了解并控制洗涤剂在膜蛋白稳定性和聚集方面所起的作用以及蛋白质 - 洗涤剂复合物的胶体性质。所有膜蛋白的X射线级晶体都是从洗涤剂增溶的蛋白制剂中生长出来的,其中膜中的异质天然脂质已被均匀的洗涤剂环境所取代。正是这种膜蛋白单分散、各向同性溶液的制备使得常用于可溶性蛋白的标准结晶方法得以成功应用。在这篇综述中,我们讨论了蛋白质纯化和样品制备的问题以及膜蛋白结晶方法的新改进。还讨论了洗涤剂以胶束或蛋白质 - 洗涤剂聚集体形式存在时的物理行为如何影响结晶以及已发表方案对新膜蛋白系统的适应性。总的结论是,如果能够在合适的洗涤剂系统中制备出纯的和单分散的制剂,许多整合膜蛋白是可以结晶的。