Chen Robert J, Bangsaruntip Sarunya, Drouvalakis Katerina A, Kam Nadine Wong Shi, Shim Moonsub, Li Yiming, Kim Woong, Utz Paul J, Dai Hongjie
Department of Chemistry, Stanford University, Stanford, CA 94305, USA.
Proc Natl Acad Sci U S A. 2003 Apr 29;100(9):4984-9. doi: 10.1073/pnas.0837064100. Epub 2003 Apr 15.
Novel nanomaterials for bioassay applications represent a rapidly progressing field of nanotechnology and nanobiotechnology. Here, we present an exploration of single-walled carbon nanotubes as a platform for investigating surface-protein and protein-protein binding and developing highly specific electronic biomolecule detectors. Nonspecific binding on nanotubes, a phenomenon found with a wide range of proteins, is overcome by immobilization of polyethylene oxide chains. A general approach is then advanced to enable the selective recognition and binding of target proteins by conjugation of their specific receptors to polyethylene oxide-functionalized nanotubes. This scheme, combined with the sensitivity of nanotube electronic devices, enables highly specific electronic sensors for detecting clinically important biomolecules such as antibodies associated with human autoimmune diseases.
用于生物测定应用的新型纳米材料代表了纳米技术和纳米生物技术中一个快速发展的领域。在此,我们展示了对单壁碳纳米管的探索,将其作为研究表面蛋白与蛋白-蛋白结合以及开发高特异性电子生物分子探测器的平台。通过固定聚环氧乙烷链可克服纳米管上的非特异性结合,这一现象在多种蛋白质中都有发现。然后提出了一种通用方法,通过将目标蛋白的特异性受体与聚环氧乙烷功能化纳米管结合,实现对目标蛋白的选择性识别和结合。该方案与纳米管电子器件的灵敏度相结合,能够制造出高特异性电子传感器,用于检测临床上重要的生物分子,如与人类自身免疫性疾病相关的抗体。