Connolly Damian, O'Shea Vincent, Clark Paul, O'Connor Brendan, Paull Brett
Centre for Bioanalytical Sciences, School of Chemical Sciences, Dublin City University, Glasnevin, Dublin, Ireland.
J Sep Sci. 2007 Nov;30(17):3060-8. doi: 10.1002/jssc.200700365.
Capacitively coupled contactless conductivity detection (C4D) is presented as a novel and versatile means of visualising discrete zones of charged functional groups grafted onto polymer based monoliths. Monoliths were first formed within 100 microm UV-transparent fused silica capillaries. Photografting methods were subsequently used to graft a charged functional monomer, 2-acrylamido-2-methyl-1-propanesulfonic acid, onto discrete regions of the monolith using a photomask. Post-modification monolith evaluation involves scanning the C4D detector along the length of the monolith to obtain a profile of the exact spatial location of grafted charged functionalities with millimetre accuracy. The methodology was extended to the visualisation of several zones of immobilised protein (bovine serum albumin) using photografted azlactone groups to enable covalent attachment of the protein to the monolith at precise locations along its length. In addition, the extent of non-specific binding of protein to the ungrafted regions of the monolith due to hydrophobic interactions could be monitored as an increase in background conductivity of the stationary phase. Finally, the technique was cross-validated using digital photography in combination with a UV light source by immobilising green fluorescent protein in discrete zones and comparing the results obtained using both complementary techniques.
电容耦合非接触式电导检测(C4D)被提出作为一种新颖且通用的方法,用于可视化接枝到聚合物整体柱上的带电官能团离散区域。整体柱首先在100微米的紫外透明熔融石英毛细管内形成。随后使用光接枝方法,通过光掩模将带电功能单体2-丙烯酰胺基-2-甲基-1-丙磺酸接枝到整体柱的离散区域上。修饰后整体柱的评估包括沿着整体柱的长度扫描C4D检测器,以获得接枝带电官能团精确空间位置的轮廓,精度可达毫米级。该方法被扩展用于可视化固定化蛋白质(牛血清白蛋白)的多个区域,使用光接枝的氮杂环丙烷基团使蛋白质能够在沿其长度的精确位置与整体柱共价连接。此外,由于疏水相互作用导致蛋白质与整体柱未接枝区域的非特异性结合程度,可以通过固定相背景电导率的增加来监测。最后,通过将绿色荧光蛋白固定在离散区域,并比较使用这两种互补技术获得的结果,使用数字摄影结合紫外光源对该技术进行了交叉验证。