Mus-Veteau Isabelle
Laboratoire de Physiologie Cellulaire et Moléculaire, UMR-CNRS 6548, Université de Nice-Sophia Antipolis, Parc Valrose Nice cedex 2, 06108 France.
Comp Funct Genomics. 2002;3(6):511-7. doi: 10.1002/cfg.218.
Membrane proteins (MPs) are responsible for the interface between the exterior and the interior of the cell. These proteins are implicated in numerous diseases, such as cancer, cystic fibrosis, epilepsy, hyperinsulinism, heart failure, hypertension and Alzheimer's disease. However, studies on these disorders are hampered by a lack of structural information about the proteins involved. Structural analysis requires large quantities of pure and active proteins. The majority of medically and pharmaceutically relevant MPs are present in tissues at very low concentration, which makes heterologous expression in large-scale production-adapted cells a prerequisite for structural studies. Obtaining mammalian MP structural data depends on the development of methods that allow the production of large quantities of MPs. This review focuses on the different heterologous expression systems, and the purification strategies, used to produce large amounts of pure mammalian MPs for structural proteomics.
膜蛋白(MPs)负责细胞外部与内部之间的界面。这些蛋白质与多种疾病有关,如癌症、囊性纤维化、癫痫、高胰岛素血症、心力衰竭、高血压和阿尔茨海默病。然而,由于缺乏有关所涉及蛋白质的结构信息,对这些疾病的研究受到了阻碍。结构分析需要大量纯净且有活性的蛋白质。大多数与医学和药学相关的膜蛋白在组织中的浓度非常低,这使得在适应大规模生产的细胞中进行异源表达成为结构研究的先决条件。获取哺乳动物膜蛋白结构数据依赖于能够大量生产膜蛋白的方法的开发。本综述重点关注用于为结构蛋白质组学大量生产纯净哺乳动物膜蛋白的不同异源表达系统和纯化策略。