Abstract − Analytical Sciences, 34(3), 317 (2018).
A Sol-gel Integrated Dual-readout Microarray Platform for Quantification and Identification of Prostate-specific Antigen
  SangWook LEE,*1,*5 Jong Hyun LEE,*2 Hyuck Gi KWON,*2 Thomas LAURELL,*3 Ok Chan JEONG,*2,*4 and Soyoun KIM*5
  *1 Department of Chemistry, University of Tokyo, Tokyo 113-0033, Japan
*2 Institute of Digital Anti-Aging Healthcare, Inje University, Gimhae 50834, Korea
*3 Department of Biomedical Engineering, Lund University, Lund SE-221 00, Sweden
*4 Department of Biomedical Engineering, Inje University, Gimhae 50834, Korea
*5 Department of Biomedical Engineering, Dongguk University, 10326, Korea
  *2 Institute of Digital Anti-Aging Healthcare, Inje University, Gimhae 50834, Korea
*3 Department of Biomedical Engineering, Lund University, Lund SE-221 00, Sweden
*4 Department of Biomedical Engineering, Inje University, Gimhae 50834, Korea
*5 Department of Biomedical Engineering, Dongguk University, 10326, Korea
Here, we report a sol-gel integrated affinity microarray for on-chip matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS) that enables capture and identification of prostate?specific antigen (PSA) in samples.  An anti-PSA antibody (H117) was mixed with a sol?gel, and the mixture was spotted onto a porous silicon (pSi) surface without additional surface modifications.  The antibody easily penetrates the sol-gel macropore fluidic network structure, making possible high affinities.  To assess the capture affinity of the platform, we performed a direct assay using fluorescein isothiocyanate-labeled PSA.  Pure PSA was subjected to on-chip MALDI-TOF-MS analysis, yielding three clear mass peptide peaks (m/z = 1272, 1407, and 1872).  The sol-gel microarray platform enables dual readout of PSA both fluorometric and MALDI-TOF MS analysis in biological samples.  Here we report a useful method for a means for discovery of biomarkers in complex body fluids.
  
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