Bao Y Paul, Wei Tai-Fen, Lefebvre Phil A, An Hao, He Liangxiu, Kunkel Gregory T, Müller Uwe R
Nanosphere, Inc., 4088 Commercial Avenue, Northbrook, Illinois 60062, USA.
Anal Chem. 2006 Mar 15;78(6):2055-9. doi: 10.1021/ac051798d.
We describe a new format for the recently introduced bio bar code technology, which improves the dose response over 10,000-fold and thereby makes this technique analytically useful. Unlike other ultrasensitive protein detection methods, such as immuno-PCR or immuno-RCA, the bio bar code technique does not employ any enzymes to achieve detection limits in the attomolar range. By sandwiching a target between a magnetic bead and an amplifier nanoparticle, a multiplicity of bar code oligonucleotides are released for each captured target analyte. These surrogate bar code targets are then hybridized to microarrays and detected with silver-amplified gold nanoparticle probes. Using PSA detection as a model, we demonstrate a linear dose response over at least 4 orders of magnitude in both target concentration and concomitant signal and a 1000-fold improvement in detection limit compared to the best ELISA system.
我们描述了一种用于最近推出的生物条形码技术的新形式,它将剂量响应提高了10000倍以上,从而使该技术在分析上具有实用性。与其他超灵敏蛋白质检测方法,如免疫PCR或免疫滚环扩增不同,生物条形码技术不使用任何酶来实现阿托摩尔范围内的检测限。通过将靶标夹在磁珠和放大纳米颗粒之间,每个捕获的靶标分析物会释放出多个条形码寡核苷酸。然后将这些替代条形码靶标与微阵列杂交,并用银增强金纳米颗粒探针进行检测。以PSA检测为模型,我们证明在靶标浓度和伴随信号方面至少有4个数量级的线性剂量响应,并且与最佳ELISA系统相比,检测限提高了1000倍。