We present a quantification method for affinity-based DNA microarrays which is based on the real-time measurements of hybridization kinetics. This method, i.e. real-time DNA microarrays, enhances the detection dynamic range of conventional systems by being impervious to probe saturation in the capturing spots, washing artifacts, microarray spot-to-spot variations, and other signal amplitude-affecting non-idealities. We demonstrate in both theory and practice that the time-constant of target capturing in microarrays, similar to all affinity-based biosensors, is inversely proportional to the concentration of the target analyte, which we subsequently use as the fundamental parameter to estimate the concentration of the analytes. Furthermore, to empirically validate the capabilities of this method in practical applications, we present a FRET-based assay which enables the real-time detection in gene expression DNA microarrays.
机构:
Iowa State Univ, Dept Elect & Comp Engn, Ames, IA 50011 USAIowa State Univ, Dept Elect & Comp Engn, Ames, IA 50011 USA
Liu, Mingdian
Monshat, Hosein
论文数: 0引用数: 0
h-index: 0
机构:
Iowa State Univ, Dept Mech Engn, Ames, IA 50011 USAIowa State Univ, Dept Elect & Comp Engn, Ames, IA 50011 USA
Monshat, Hosein
Zhao, Yuxin
论文数: 0引用数: 0
h-index: 0
机构:
Iowa State Univ, Dept Chem & Biomol Engn, Ames, IA 50011 USA
Nankai Univ, Minist Educ, Key Lab Mol Microbiol & Technol, Tianjin 300071, Peoples R ChinaIowa State Univ, Dept Elect & Comp Engn, Ames, IA 50011 USA
Zhao, Yuxin
Lu, Meng
论文数: 0引用数: 0
h-index: 0
机构:
Iowa State Univ, Dept Elect & Comp Engn, Ames, IA 50011 USA
Iowa State Univ, Dept Mech Engn, Ames, IA 50011 USAIowa State Univ, Dept Elect & Comp Engn, Ames, IA 50011 USA