Institute of Biochemistry, Biocenter, Goethe-University Frankfurt, Frankfurt am Main, Germany.
PLoS One. 2013 Jun 25;8(6):e67112. doi: 10.1371/journal.pone.0067112. Print 2013.
Many interesting and important membrane proteins are hetero-oligomeric. However, besides naturally abundant examples, the structures of relatively few such complexes are known. Partly, this is due to difficulties in expression, stoichiometric assembly, and in the evaluation of their stability prior to crystallization trials. Here we describe a new approach, which allows rapid assessment of protein complex quality, assembly and stoichiometry, simplifying the search for conditions conducive to long-term stability and crystallization. Multicolour fluorescence size-exclusion chromatography (MC-FSEC) is used to enable tracking of individual subunits through expression, solubilization and purification steps. We show how the method has been applied to the heterodimeric transporter associated with antigen processing (TAP) and demonstrate how it may be extended in order to analyse membrane multisubunit assemblies.
许多有趣且重要的膜蛋白都是异源寡聚体。然而,除了天然丰富的例子外,相对较少的此类复合物的结构是已知的。部分原因是在结晶试验之前,这些复合物在表达、化学计量组装和稳定性评估方面存在困难。在这里,我们描述了一种新方法,该方法可以快速评估蛋白质复合物的质量、组装和化学计量,简化了寻找有利于长期稳定性和结晶的条件的过程。多色荧光体积排阻色谱 (MC-FSEC) 用于跟踪单个亚基在表达、溶解和纯化步骤中的变化。我们展示了该方法如何应用于抗原加工相关转运体 (TAP) 异二聚体,并演示了如何扩展该方法以分析膜多亚基组装。