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原子力显微镜研究免疫传感器表面以缩小 ELISA 型传感器的尺寸。

Atomic force microscopy study of immunosensor surface to scale down the size of ELISA-type sensors.

机构信息

Department of Physics, Clarkson University, Potsdam, NY 13699, USA.

出版信息

Nanotechnology. 2010 Apr 9;21(14):145503. doi: 10.1088/0957-4484/21/14/145503. Epub 2010 Mar 16.

Abstract

Here we describe the use of atomic force microscopy (AFM) to study the nanoscale mechanics of the molecular layers of a popular immunosensor, ELISA (enzyme-linked immunosorbent assay) type. We characterize the sensor surface in terms of brush length and grafting density of the molecular layers. The obtained data demonstrated that a reliable reading of the immunosignal (a suggested dimensionless combination of brush length and grafting density) can be attained from an area as small as approximately 3 microm(2). This is approximately 4 million times smaller compared to typical ELISA sensors. The immunosensor described is composed of a molecular mix of two different antigens. Intriguingly, we find that AFM can reliably distinguish between having the immunosignal from either antibody and from both antibodies together. This was impossible to get by using standard optical detection methods.

摘要

在这里,我们描述了原子力显微镜(AFM)在研究一种流行的免疫传感器(酶联免疫吸附测定(ELISA)型)的分子层的纳米力学方面的应用。我们根据分子层的刷长和接枝密度来描述传感器表面。所获得的数据表明,可以从大约 3 微米(2)的小面积获得免疫信号(刷长和接枝密度的无量纲组合)的可靠读数。与典型的 ELISA 传感器相比,这大约小了 400 万倍。所描述的免疫传感器由两种不同抗原的分子混合物组成。有趣的是,我们发现 AFM 可以可靠地区分来自任一抗体和来自两种抗体的免疫信号。这是使用标准的光学检测方法无法实现的。

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