Chen Hsiu-Mei, Huang Tsun-Han, Tsai Ruey-Ming
Department of Chemical Engineering, National Taiwan University of Science and Technology, Taipei 10607, Taiwan.
Anal Biochem. 2009 Sep 1;392(1):1-7. doi: 10.1016/j.ab.2009.05.029. Epub 2009 May 22.
A biotin-coated quartz crystal microbalance (QCM) chip was prepared by dip-coating a long-chain alkanethiol-modified crystal with precoupled dextran-biotin hydrogels. The resulting biotin chip was used to affinity-immobilize streptavidin (SAv) and was then further employed for various biosensor assays. First, the SAv chip allowed efficient on-line binding of biotinylated bovine serum albumin (bBSA), followed by a sensitive and specific response toward anti-bovine serum albumin (BSA) antibodies. Three consecutive immunoassays were reproducibly demonstrated with a single chip. The apparent binding kinetics with k(on)=5.9 microM(-1) h(-1), k(off)=10.1 h(-1), and K(D)=1.71 microM was readily resolved by fitting the real-time sensorgrams. Second, the capability of the SAv chip to selectively recognize recombinant Escherichia coli with flagella displaying an artificial SAv binding peptide, Strep-tag II, was demonstrated by QCM analysis and verified by scanning transmission electron microscope (STEM) image analysis with biotin-coated gold nanoparticles as the label. Finally, the affinity of the cell-displayed Strep-tag II peptide to surface-coated SAv, K(D)=6.8 x 10(8) CFU/ml, was resolved on-line using equilibrium binding kinetics by QCM. This study presents an easy, economical, and reliable method of preparing high-performance SAv-coated biotin chips with potential for application in real-time repetitive immunoassays, on-line binding kinetics studies, and high-affinity peptide screening.
通过将预偶联葡聚糖 - 生物素水凝胶的长链烷硫醇修饰晶体进行浸涂,制备了生物素包被的石英晶体微天平(QCM)芯片。所得的生物素芯片用于亲和固定链霉亲和素(SAv),然后进一步用于各种生物传感器检测。首先,SAv芯片允许生物素化牛血清白蛋白(bBSA)高效在线结合,随后对抗牛血清白蛋白(BSA)抗体产生灵敏且特异的响应。使用单个芯片可重复地进行三次连续免疫检测。通过拟合实时传感图,很容易解析出表观结合动力学,其结合速率常数k(on)=5.9 microM(-1) h(-1),解离速率常数k(off)=10.1 h(-1),解离常数K(D)=1.71 microM。其次,通过QCM分析证明了SAv芯片选择性识别带有展示人工SAv结合肽Strep-tag II的鞭毛的重组大肠杆菌的能力,并通过以生物素包被的金纳米颗粒为标记的扫描透射电子显微镜(STEM)图像分析进行了验证。最后,使用QCM通过平衡结合动力学在线解析细胞展示的Strep-tag II肽与表面包被的SAv的亲和力,K(D)=6.8 x 10(8) CFU/ml。本研究提出了一种简便、经济且可靠的制备高性能SAv包被生物素芯片的方法,该方法具有在实时重复免疫检测、在线结合动力学研究和高亲和力肽筛选中应用的潜力。