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Impact Factor: 10.3
DOI number: 10.1007/s12274-021-3588-4
Journal: Nano Research
Key Words: adsorption-induced inactivation early cancer detection nanobody-based biosensor stress enhancement tumor markers
Abstract: Early cancer diagnosis requires ultrasensitive detection of tumor markers in blood. To this end, we develop a novel microcantilever immunosensor using nanobodies (Nbs) as receptors. As the smallest antibody (Ab) entity comprising an intact antigen-binding site, Nbs achieve dense receptor layers and short distances between antigen-binding regions and sensor surfaces, which significantly elevate the generation and transmission of surface stress. Owing to the inherent thiol group at the C-terminus, Nbs are covalently immobilized on microcantilever surfaces in directed orientation via one-step reaction, which further enhances the stress generation. For microcantilever-based nanomechanical sensor, these advantages dramatically increase the sensor sensitivity. Thus, Nb-functionalized microcantilevers can detect picomolar concentrations of tumor markers with three orders of magnitude higher sensitivity, when compared with conventional Ab-functionalized microcantilevers. This proof-of-concept study demonstrates an ultrasensitive, label-free, rapid, and low-cost method for tumor marker detection. Moreover, interestingly, we find Nb inactivation on sensor interfaces when using macromolecule blocking reagents. The adsorption-induced inactivation is presumably caused by the change of interfacial properties, due to binding site occlusion upon complex coimmobilization formations. Our findings are generalized to any coimmobilization methodology for Nbs and, thus, for the construction of high-performance immuno-surfaces.
First Author: Rao Depeng,Mei Kainan
Indexed by: Journal paper
Correspondence Author: Zhang Qingchuan*,Wu Shangquan*
Volume: 15
Page Number: 1003-1012
Translation or Not: no
Date of Publication: 2022-02-01
Included Journals: SCI
Links to published journals: https://link.springer.com/article/10.1007/s12274-021-3588-4