Huang Yi, Shan Wei, Liu Baohong, Liu Yun, Zhang Yahong, Zhao Yue, Lu Haojie, Tang Yi, Yang Pengyuan
Department of Chemistry, Fudan University, Shanghai 200433, People's Republic of China.
Lab Chip. 2006 Apr;6(4):534-9. doi: 10.1039/b517590a. Epub 2006 Feb 28.
An enzymatic microreactor has been fabricated based on the poly(methyl methacrylate) (PMMA) microchchip surface-modified with zeolite nanoparticles. By introducing the silanol functional groups, the surface of PMMA microchannel has been successfully modified with silicalite-1 nanoparticle for the first time due to its large external surface area and high dispersibility in solutions. Trypsin can be stably immobilized in the microchannel to form a bioreactor using silica sol-gel matrix. The immobilization of enzyme can be realized with a stable gel network through a silicon-oxygen-silicon bridge via tethering to those silanol groups, which has been investigated by scanning electron microscopy and microchip capillary electrophoresis with laser-induced fluorescence detection. The maximum proteolytic rate constant of the immobilized trypsin is measured to be about 6.6 mM s(-1). Using matrix assisted laser desorption and ionization time-of-flight mass spectrometry, the proposed microreactor provides an efficient digestion of cytochrome c and bovine serum albumin at a fast flow rate of 4.0 microL min(-1), which affords a very short reaction time of less than 5 s.
基于用沸石纳米颗粒表面改性的聚甲基丙烯酸甲酯(PMMA)微芯片制造了一种酶促微反应器。通过引入硅醇官能团,由于硅沸石-1纳米颗粒具有大的外表面面积和在溶液中的高分散性,首次成功地用其对PMMA微通道表面进行了改性。使用硅溶胶-凝胶基质,胰蛋白酶可以稳定地固定在微通道中以形成生物反应器。酶的固定可以通过与那些硅醇基团连接形成的硅-氧-硅桥的稳定凝胶网络来实现,这已通过扫描电子显微镜和激光诱导荧光检测的微芯片毛细管电泳进行了研究。测得固定化胰蛋白酶的最大蛋白水解速率常数约为6.6 mM s(-1)。使用基质辅助激光解吸和电离飞行时间质谱,所提出的微反应器在4.0 μL min(-1)的快速流速下对细胞色素c和牛血清白蛋白进行了高效消化,反应时间非常短,不到5秒。