Sharma Pooja, Kaywan-Lutfi Mariam, Krshnan Logesvaran, Byrne Eamon F X, Call Melissa Joy, Call Matthew Edwin
Structural Biology Division, The Walter and Eliza Hall Institute of Medical Research, Australia.
J Vis Exp. 2013 Mar 6(73):e50141. doi: 10.3791/50141.
Physical interactions among the lipid-embedded alpha-helical domains of membrane proteins play a crucial role in folding and assembly of membrane protein complexes and in dynamic processes such as transmembrane (TM) signaling and regulation of cell-surface protein levels. Understanding the structural features driving the association of particular sequences requires sophisticated biophysical and biochemical analyses of TM peptide complexes. However, the extreme hydrophobicity of TM domains makes them very difficult to manipulate using standard peptide chemistry techniques, and production of suitable study material often proves prohibitively challenging. Identifying conditions under which peptides can adopt stable helical conformations and form complexes spontaneously adds a further level of difficulty. Here we present a procedure for the production of homo- or hetero-dimeric TM peptide complexes from materials that are expressed in E. coli, thus allowing incorporation of stable isotope labels for nuclear magnetic resonance (NMR) or non-natural amino acids for other applications relatively inexpensively. The key innovation in this method is that TM complexes are produced and purified as covalently associated (disulfide-crosslinked) assemblies that can form stable, stoichiometric and homogeneous structures when reconstituted into detergent, lipid or other membrane-mimetic materials. We also present carefully optimized procedures for expression and purification that are equally applicable whether producing single TM domains or crosslinked complexes and provide advice for adapting these methods to new TM sequences.
膜蛋白中嵌入脂质的α-螺旋结构域之间的物理相互作用在膜蛋白复合物的折叠和组装以及跨膜(TM)信号传导和细胞表面蛋白水平调节等动态过程中起着关键作用。了解驱动特定序列缔合的结构特征需要对TM肽复合物进行复杂的生物物理和生化分析。然而,TM结构域的极端疏水性使得使用标准肽化学技术对其进行操作非常困难,并且合适的研究材料的生产往往被证明具有极高的挑战性。确定肽能够采用稳定螺旋构象并自发形成复合物的条件又增加了一层难度。在此,我们展示了一种从在大肠杆菌中表达的材料生产同二聚体或异二聚体TM肽复合物的方法,从而能够以相对较低的成本掺入用于核磁共振(NMR)的稳定同位素标记或用于其他应用的非天然氨基酸。该方法的关键创新之处在于,TM复合物作为共价结合(二硫键交联)的组装体进行生产和纯化,当重新组装到去污剂、脂质或其他膜模拟材料中时,能够形成稳定、化学计量和均匀的结构。我们还展示了经过精心优化的表达和纯化程序,无论生产单个TM结构域还是交联复合物,这些程序都同样适用,并为将这些方法应用于新的TM序列提供建议。