Department of Biochemistry Groningen Biomolecular Sciences and Biotechnology Institute, University of Groningen, Nijenborgh 4, 9747 AG, Groningen, The Netherlands.
Mol Cell Proteomics. 2011 Jul;10(7):M000052MCP200. doi: 10.1074/mcp.M000052-MCP200.
Biochemical and biophysical characterization of CFTR (the cystic fibrosis transmembrane conductance regulator) is thwarted by difficulties to obtain sufficient quantities of correctly folded and functional protein. Here we have produced human CFTR in the prokaryotic expression host Lactococcus lactis. The full-length protein was detected in the membrane of the bacterium, but the yields were too low (< 0.1% of membrane proteins) for in vitro functional and structural characterization, and induction of the expression of CFTR resulted in growth arrest. We used isobaric tagging for relative and absolute quantitation based quantitative proteomics to find out why production of CFTR in L. lactis was problematic. Protein abundances in membrane and soluble fractions were monitored as a function of induction time, both in CFTR expression cells and in control cells that did not express CFTR. Eight hundred and forty six proteins were identified and quantified (35% of the predicted proteome), including 163 integral membrane proteins. Expression of CFTR resulted in an increase in abundance of stress-related proteins (e.g. heat-shock and cell envelope stress), indicating the presence of misfolded proteins in the membrane. In contrast to the reported consequences of membrane protein overexpression in Escherichia coli, there were no indications that the membrane protein insertion machinery (Sec) became overloaded upon CFTR production in L. lactis. Nutrients and ATP became limiting in the control cells as the culture entered the late exponential and stationary growth phases but this did not happen in the CFTR expressing cells, which had stopped growing upon induction. The different stress responses elicited in E. coli and L. lactis upon membrane protein production indicate that different strategies are needed to overcome low expression yields and toxicity.
CFTR(囊性纤维化跨膜电导调节因子)的生化和生物物理特性分析受到难以获得大量正确折叠和有功能的蛋白质的阻碍。在这里,我们在原核表达宿主乳球菌中生产了人 CFTR。全长蛋白被检测到存在于细菌的膜中,但产量太低(<膜蛋白的 0.1%),无法进行体外功能和结构特性分析,并且 CFTR 的表达诱导导致生长停滞。我们使用基于相对和绝对定量的同量异位标记定量蛋白质组学来找出为什么在乳球菌中生产 CFTR 会出现问题。在 CFTR 表达细胞和不表达 CFTR 的对照细胞中,作为诱导时间的函数,监测膜和可溶部分中的蛋白质丰度。鉴定和定量了 846 种蛋白质(预测蛋白质组的 35%),包括 163 种完整的膜蛋白。CFTR 的表达导致应激相关蛋白(例如热休克和细胞包膜应激)的丰度增加,表明膜中存在错误折叠的蛋白质。与在大肠杆菌中膜蛋白过表达的报道后果相反,在乳球菌中生产 CFTR 时,膜蛋白插入机制(Sec)并没有过载的迹象。在对照细胞中,当培养物进入指数晚期和静止生长阶段时,营养物质和 ATP 变得有限,但在 CFTR 表达细胞中没有发生这种情况,CFTR 诱导后细胞停止生长。在生产膜蛋白时,大肠杆菌和乳球菌中引发的不同应激反应表明,需要采取不同的策略来克服低表达产量和毒性。