Biotechnology Industrialization Center, National Institute of Advanced Industrial Science and Technology (AIST), c/o Katayanagi Advanced Research Laboratories, Tokyo University of Technology, 1404-1 Katakura, Hachioji, Tokyo 192-0982, Japan.
Biosens Bioelectron. 2011 Apr 15;26(8):3696-9. doi: 10.1016/j.bios.2011.02.007. Epub 2011 Feb 16.
We have established a highly sensitive and selective protein detection technology in combination with the nanofabrication technique. A silica nanopillar chip with a 200-nm pitch and 1000-nm height pillar substrate was fabricated by electron beam lithography and deep reactive ion etching method. Fluorescent peptides, with high affinity towards vascular endothelial growth factor (VEGF), were immobilized on nanopillar chip via a self-assembled monolayer made from 3-aminopropyltrimethoxysilane and glutaraldehyde under optimal conditions. The fluorescence intensity of the fluorescent peptide on the nanopillar substrate increased with increasing VEGF concentrations, as determined by a fluorescence spectrophotometer and fluorescent scanning image analysis. The dissociation constant (K(d) value) calculated by the non-linear least square curve fitting method was 6.0 × 10(-9)M, which contributed to the highly sensitive detection of VEGF. The fluorescence intensity of the fluorescent reagent on the nanopillar substrate upon binding to VEGF was higher than that obtained using the flat substrate because the dense and tall nanopillar array increased the virtual protein binding area. The reproducibility tests and lifetime measurement indicate the fluorescent reagent to be a useful biosensor for the detection of VEGF in this system. These experimental results clearly showed that the combination of a fluorescent reagent and a nanopillar substrate may be widely applicable as a convenient method for the detection of VEGF.
我们结合纳米制造技术建立了一种高度灵敏和选择性的蛋白质检测技术。通过电子束光刻和深反应离子刻蚀方法,制造了具有 200nm 间距和 1000nm 高支柱基底的二氧化硅纳米柱芯片。荧光肽通过 3-氨丙基三甲氧基硅烷和戊二醛制成的自组装单层固定在纳米柱芯片上,在最佳条件下对血管内皮生长因子(VEGF)具有高亲和力。通过荧光分光光度计和荧光扫描图像分析,确定纳米柱基底上荧光肽的荧光强度随 VEGF 浓度的增加而增加。通过非线性最小二乘曲线拟合方法计算的离解常数(Kd 值)为 6.0×10-9M,有助于对 VEGF 进行高灵敏度检测。与使用平面基底相比,由于密集且高大的纳米柱阵列增加了虚拟蛋白质结合面积,因此与 VEGF 结合后,纳米柱基底上荧光试剂的荧光强度更高。重复性测试和寿命测量表明,荧光试剂是该系统中检测 VEGF 的有用生物传感器。这些实验结果清楚地表明,荧光试剂和纳米柱基底的结合可以作为一种方便的 VEGF 检测方法广泛应用。