Dipartimento di Biotecnologie Mediche e Medicina Traslazionale, Università degli Studi di Milano, 20090 Segrate, Italy.
Proc Natl Acad Sci U S A. 2013 Jun 4;110(23):9350-5. doi: 10.1073/pnas.1214589110. Epub 2013 May 21.
Recognizing and quantifying specific biomolecules in aqueous samples are constantly needed in research and diagnostic laboratories. As the typical detection procedures are rather lengthy and involve the use of labeled secondary antibodies or other agents to provide a signal, efforts have been made over the last 10 y to develop alternative label-free methods that enable direct detection. We propose and demonstrate an extremely simple, low-cost, label-free biodetector based on measuring the intensity of light reflected by the interface between a fluid sample and an amorphous fluoropolymer substrate having a refractive index very close to that of water and hosting various antibodies immobilized in spots. Under these index-matching conditions, the amount of light reflected by the interface allows straightforward quantification of the amount of antigen binding to each spot. Using antibodies targeting heterologous immunoglobulins and antigens commonly used as markers for diagnoses of hepatitis B and HIV, we demonstrate the limit of detection of a few picograms per square millimeter of surface-bound molecules. We also show that direct and real-time access to the amount of binding molecules allows the precise extrapolation of adhesion rates, from which the concentrations of antigens in solution can be estimated down to fractions of nanograms per milliliter.
在研究和诊断实验室中,经常需要识别和定量水样中的特定生物分子。由于典型的检测程序相当冗长,并且涉及使用标记的二级抗体或其他试剂来提供信号,因此在过去 10 年中,人们一直在努力开发替代的无标记方法,以实现直接检测。我们提出并演示了一种极其简单、低成本、无标记的生物探测器,它基于测量流体样品与具有非常接近水折射率的无定形氟聚合物基底之间界面反射光的强度,基底上固定有各种抗体。在这些折射率匹配条件下,界面反射的光量可以直接定量与每个斑点结合的抗原量。使用针对异源免疫球蛋白和作为乙型肝炎和 HIV 诊断标志物的常见抗原的抗体,我们证明了每平方毫米表面结合分子的几个皮克的检测限。我们还表明,直接实时访问结合分子的数量可以精确推断粘附速率,从而可以估计溶液中抗原的浓度低至纳克每毫升的分数。