Label-Free Sub-picomolar Protein Detection with Field-Effect Transistors

被引:55
作者
Estrela, Pedro [1 ]
Paul, Debjani [1 ]
Song, Qifeng [2 ]
Stadler, Lukas K. J. [2 ]
Wang, Ling [3 ]
Huq, Ejaz [3 ]
Davis, Jason J. [4 ]
Ferrigno, Paul Ko [2 ]
Migliorato, Piero [1 ]
机构
[1] Univ Cambridge, Dept Engn, Elect Engn Div, Cambridge CB3 0FA, England
[2] St James Univ Hosp, Leeds Inst Mol Med, Leeds LS9 7TF, W Yorkshire, England
[3] Rutherford Appleton Lab, Cent Microstruct Facil, Didcot OX11 0QX, Oxon, England
[4] Univ Oxford, Dept Chem, Phys & Theoret Chem Lab, Oxford OX1 3QZ, England
基金
英国生物技术与生命科学研究理事会;
关键词
PEPTIDE APTAMERS; SENSORS; MICROARRAYS; SCAFFOLD; ARRAYS;
D O I
10.1021/ac902554v
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Proteins mediate the bulk of biological activity and are powerfully assayed in the diagnosis of diseases. Protein detection relies largely on antibodies, which have significant technical limitations especially when immobilized on two-dimensional surfaces. Here, we report the integration of peptide aptamers with extended gate metal-oxide-semiconductor field-effect transistors (MOSFETs) to achieve label-free sub-picomolar target protein detection. Specifically, peptide aptamers that recognize highly related protein partners of the cyclin-dependent kinase (CDK) family are immobilized on the transistor gate to enable human CDK2 to be detected at 100 fM or 5 pg/mL, well within the clinically relevant range. The target specificity, ease of fabrication, and scalability of these FET arrays further demonstrate the potential application of the multiplexable field effect format to protein sensing.
引用
收藏
页码:3531 / 3536
页数:6
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