Department of Chemistry and Research Institute of Physics and Chemistry (RINPAC), Chonbuk National University, Jeonju 561-756, South Korea.
Analyst. 2009 May;134(5):933-8. doi: 10.1039/b822094h. Epub 2009 Mar 2.
This paper describes a single-molecule sandwich immunoassay method that utilizes total internal reflection fluorescence microscopy (TIRFM) at the single-molecule level for nanoarray protein chip applications. Nanoarray patterning of a biotin-probe with a spot diameter of 179 +/- 1 nm was performed successfully on a (3-mercaptopropyl)trimethoxysilane (MPTMS)-coated glass substrate by atomic force microscopy (AFM). The formation of biotin patterns was confirmed directly by observing the heights of bound streptavidin and biotin-antibody on glass substrates using an AFM in contact mode. Target protein molecules (or antigen) at the zepto-molar (zM) concentration level (x 10(-21) M) were detected on MPTMS-coated glass nanoarray protein chips by TIRFM. Finally, cytokine clinical samples (i.e. TNF-alpha and IL-1alpha) as cancer marker protein molecules were applied to nanoarray protein chips, and detection limits were at 600 zM.
本文描述了一种单分子夹心免疫测定方法,该方法利用全内反射荧光显微镜(TIRFM)在单分子水平上进行纳米阵列蛋白质芯片应用。通过原子力显微镜(AFM)成功地在(3-巯丙基)三甲氧基硅烷(MPTMS)涂覆的玻璃基底上进行了具有 179 +/- 1nm 点直径的生物素探针的纳米阵列图案化。通过在接触模式下使用 AFM 直接观察玻璃基底上结合的链霉亲和素和生物素-抗体的高度,直接确认了生物素图案的形成。在 MPTMS 涂覆的玻璃纳米阵列蛋白质芯片上,通过 TIRFM 检测到兆分摩尔(zM)浓度水平(x 10(-21) M)的目标蛋白质分子(或抗原)。最后,将细胞因子临床样品(即 TNF-alpha 和 IL-1alpha)作为癌症标志物蛋白质分子应用于纳米阵列蛋白质芯片,检测限为 600 zM。