TY - JOUR
T1 - An integrated microfluidic system for rapid screening of alpha-fetoprotein-specific aptamers
AU - Huang, Chao Jyun
AU - Lin, Hsin I.
AU - Shiesh, Shu Chu
AU - Lee, Gwo Bin
N1 - Funding Information:
The authors would like to thank the National Science Council in Taiwan (NSC 99-2120-M-007-015 ) and the “Toward A World-class University” Project for financial support of this study.
PY - 2012/5/15
Y1 - 2012/5/15
N2 - The systematic evolution of ligands by exponential enrichment (SELEX) is a screening technique that involves the progressive selection of highly specific ligands via repeated rounds of partition and amplification from a large random pool of nucleic acid sequences. The products of this selection process are called aptamers and are either short single-stranded deoxyribonucleic acid (ssDNA) or ribonucleic acid (RNA) molecules with a high binding affinity to a large variety of target analytes. However, SELEX is a lengthy, labor-intensive, iterative process requiring multiple rounds of extraction and polymerase chain reaction (PCR) amplification. In order to address these problems, this study presents a new integrated microfluidic system consisting of a magnetic bead-based microfluidic SELEX chip and a competitive assay chip to automate the aptamer screening process. More importantly, the selected ssDNA sequences were confirmed to have a high affinity and specificity to the target molecules, using the developed competitive assay chip. With this approach, an aptamer specific to alpha-fetoprotein (AFP), which is a biomarker for liver cancers, has been successfully selected. The screened aptamer was used as a recognition molecule for AFP and has a linear detection range from 12.5 to 800. ng/mL, which was suitable for rapid clinical applications.
AB - The systematic evolution of ligands by exponential enrichment (SELEX) is a screening technique that involves the progressive selection of highly specific ligands via repeated rounds of partition and amplification from a large random pool of nucleic acid sequences. The products of this selection process are called aptamers and are either short single-stranded deoxyribonucleic acid (ssDNA) or ribonucleic acid (RNA) molecules with a high binding affinity to a large variety of target analytes. However, SELEX is a lengthy, labor-intensive, iterative process requiring multiple rounds of extraction and polymerase chain reaction (PCR) amplification. In order to address these problems, this study presents a new integrated microfluidic system consisting of a magnetic bead-based microfluidic SELEX chip and a competitive assay chip to automate the aptamer screening process. More importantly, the selected ssDNA sequences were confirmed to have a high affinity and specificity to the target molecules, using the developed competitive assay chip. With this approach, an aptamer specific to alpha-fetoprotein (AFP), which is a biomarker for liver cancers, has been successfully selected. The screened aptamer was used as a recognition molecule for AFP and has a linear detection range from 12.5 to 800. ng/mL, which was suitable for rapid clinical applications.
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U2 - 10.1016/j.bios.2012.02.024
DO - 10.1016/j.bios.2012.02.024
M3 - Article
C2 - 22410487
AN - SCOPUS:84862791532
SN - 0956-5663
VL - 35
SP - 50
EP - 55
JO - Biosensors and Bioelectronics
JF - Biosensors and Bioelectronics
IS - 1
ER -