Gokarna Anisha, Jin Li-Hua, Hwang Jun Seok, Cho Yong-Hoon, Lim Yong Taik, Chung Bong Hyun, Youn Seong Hun, Choi Dong Sik, Lim Jung Hyurk
Nano-Bio-Photonics Laboratory, Department of Physics, Chungbuk National University, Cheongju, Korea.
Proteomics. 2008 May;8(9):1809-18. doi: 10.1002/pmic.200701072.
In this article, we demonstrate the fabrication and detection of cancer protein biochips consisting of micro- and nanoarrays whereby pegylated quantum dots (QDs) conjugated to antibodies (Abs) of prostate specific antigens (PSA) were used for the detection of clinical biomarkers such as PSA. BSA which acts as an efficient blocking layer in microarrays, tends to show an interaction with QDs. In view of this fact, we investigated two series of samples which were fabricated in the presence and absence of BSA blocking layer. Variation in the incubation time required for the antigen-antibody interaction to take place, different proteins as controls and the effect of bare QDs on these microarrays, were the three main parameters which were studied in these two series. Samples fabricated in the absence of BSA blocking layer exhibited an extremely high specificity in the detection of cancer proteins and were also marked by negligible nonspecific binding effects of QDs, in stark contrast to the samples fabricated using BSA as a blocking layer. Fabrication of nanoarrays of QD-conjugated PSA Abs having a spot size of nearly 900 nm has also been demonstrated. Thus, we show the potential offered by QDs in in vitro analysis of cancer biomarker imaging.
在本文中,我们展示了由微阵列和纳米阵列组成的癌症蛋白质生物芯片的制备及检测方法,其中将与前列腺特异性抗原(PSA)抗体(Abs)偶联的聚乙二醇化量子点(QDs)用于检测诸如PSA等临床生物标志物。牛血清白蛋白(BSA)在微阵列中作为有效的封闭层,往往会与量子点发生相互作用。鉴于这一事实,我们研究了在有和没有BSA封闭层的情况下制备的两个系列的样品。抗原 - 抗体相互作用发生所需的孵育时间变化、作为对照的不同蛋白质以及裸量子点对这些微阵列的影响,是在这两个系列中研究的三个主要参数。与使用BSA作为封闭层制备的样品形成鲜明对比的是,在没有BSA封闭层的情况下制备的样品在癌症蛋白质检测中表现出极高的特异性,并且量子点的非特异性结合效应也可忽略不计。还展示了制备斑点尺寸近900nm的QD偶联PSA Abs纳米阵列的方法。因此,我们展示了量子点在癌症生物标志物成像体外分析中的潜力。