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一种生物素-水凝胶包被的石英晶体微天平生物传感器及其在免疫测定和肽展示细胞检测中的应用。

A biotin-hydrogel-coated quartz crystal microbalance biosensor and applications in immunoassay and peptide-displaying cell detection.

作者信息

Chen Hsiu-Mei, Huang Tsun-Han, Tsai Ruey-Ming

机构信息

Department of Chemical Engineering, National Taiwan University of Science and Technology, Taipei 10607, Taiwan.

出版信息

Anal Biochem. 2009 Sep 1;392(1):1-7. doi: 10.1016/j.ab.2009.05.029. Epub 2009 May 22.

Abstract

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.

摘要

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。

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