Marius P, Wright J N, Findlow I S, Williamson P T F
School of Biological Sciences, University of Southampton, Basset Crescent East, Southampton SO16 7PX, UK.
Protein Expr Purif. 2010 Jul;72(1):107-12. doi: 10.1016/j.pep.2010.01.019. Epub 2010 Feb 1.
Fukutin-I is a member of a family of putative O-linked glycosyltransferases linked to the glycosylation of the dystrophin complex. Mutations in this family of proteins have been linked to a number of congenital muscular dystrophies that arise from the hypoglycosylation of alpha-dystroglycan. Critical to the function of Fukutin and other members of this family is their localisation within the cell, which has been shown to depend critically on the interactions between the N-terminal transmembrane domain of these proteins and the lipid bilayer within the ER/Golgi. To investigate how the interactions between the N-terminal transmembrane domain and the lipid bilayer regulate the localisation of Fukutin-I, we have developed an efficient expression and purification protocol in Escherichia coli to allow biophysical studies to be performed. Expressing the N-terminal domain of Fukutin-1 fused to a His(6) tag resulted in the localisation of the protein to the bacterial membrane. A purification strategy has been developed to isolate the highly hydrophobic transmembrane domain of Fukutin-1 from the membrane with yields of approximately 4 mg per litre of minimal media. Preliminary biophysical analyses have confirmed the identity of the peptide and revealed that in hydrophobic solvents mimicking the bilayer, the peptide adopts a well-structured alpha-helix as predicted from the sequence.
福库汀 -I 是一个假定的 O 连接糖基转移酶家族的成员,该家族与肌营养不良蛋白复合物的糖基化有关。这个蛋白质家族中的突变与一些由α - 肌营养不良聚糖低糖基化引起的先天性肌营养不良症有关。福库汀和该家族其他成员功能的关键在于它们在细胞内的定位,研究表明这主要取决于这些蛋白质的 N 端跨膜结构域与内质网/高尔基体中的脂质双层之间的相互作用。为了研究 N 端跨膜结构域与脂质双层之间的相互作用如何调节福库汀 -I 的定位,我们开发了一种在大肠杆菌中高效表达和纯化的方案,以便能够进行生物物理研究。表达与 His(6)标签融合的福库汀 -1 的 N 端结构域导致该蛋白质定位于细菌膜。已经开发了一种纯化策略,从膜中分离出福库汀 -1 的高度疏水的跨膜结构域,每升基本培养基的产量约为 4 毫克。初步的生物物理分析证实了该肽的身份,并表明在模拟双层的疏水溶剂中,该肽如序列预测的那样形成了结构良好的α螺旋。