Ogasawara Daisuke, Hachiya Naomi S, Kaneko Kiyotoshi, Sode Koji, Ikebukuro Kazunori
Department of Biotechnology, Tokyo University of Agriculture and Technology, 2-24-16 Naka-cho, Koganei-shi, Tokyo 184-8588, Japan.
Biosens Bioelectron. 2009 Jan 1;24(5):1372-6. doi: 10.1016/j.bios.2008.07.082. Epub 2008 Aug 20.
Aptamers are good molecular recognition elements for biosensors. Especially, their conformational change, which is induced by the binding to the target molecule, enables the development of several types of useful detection systems. We applied this property to bound/free separation, which is a crucial process for highly sensitive detection. We designed aptamers which change their conformation upon binding to the target molecule and thereby expose a single-strand bearing the complementary sequence to the capture probe immobilized onto the support. We named the designed aptamers "capturable aptamers" and the capture probe "capture DNA". Three capturable aptamers were designed based on the PrP aptamer, which binds to prion protein. One of these capturable aptamers was demonstrated to recognize prion protein and change its conformation upon binding to it. A detection system using this designed capturable aptamer for prion protein was developed. Capturable aptamers and capture DNA allow us to perform simple bound/free separation with only one target ligand.
适体是生物传感器良好的分子识别元件。特别是,它们与靶分子结合时所诱导的构象变化,使得能够开发出几种类型的有用检测系统。我们将这一特性应用于结合/游离分离,这是高灵敏度检测的关键过程。我们设计了适体,它们在与靶分子结合时会改变构象,从而暴露出与固定在载体上的捕获探针具有互补序列的单链。我们将设计的适体命名为“可捕获适体”,将捕获探针命名为“捕获DNA”。基于与朊病毒蛋白结合的PrP适体设计了三种可捕获适体。其中一种可捕获适体被证明能够识别朊病毒蛋白并在与其结合时改变其构象。开发了一种使用这种设计的朊病毒蛋白可捕获适体的检测系统。可捕获适体和捕获DNA使我们能够仅用一种靶配体进行简单的结合/游离分离。