TY - JOUR
T1 - DNA microarray-based solid-phase PCR on copoly (DMA-NAS-MAPS) silicon coated slides
T2 - An example of relevant clinical application
AU - Damin, Francesco
AU - Galbiati, Silvia
AU - Ferrari, Maurizio
AU - Chiari, Marcella
PY - 2016/4/15
Y1 - 2016/4/15
N2 - In a previous study we developed a highly sensitive DNA microarray for the detection of common KRAS oncogenic mutations, which has been proven to be highly specific in assigning the correct genotype without any enrichment strategy even in the presence of minority mutated alleles. However, in this approach, the need of a spotter for the deposition of the purified PCR products on the substrates and the purification step of the conventional PCR are serious drawbacks. To overcome these limitations we have introduced the solid-phase polymerase chain reaction (SP-PCR) to form the array of PCR products starting from the oligonucleotide primers. This work was possible thanks to the great thermal stability of the copoly (DMA-NAS-MAPS) coating which withstands PCR thermal cycling temperatures. As an example of the application of this platform we performed the analysis of six common mutations in the codon 12 of KRAS gene (G12A, G12C, G12D, G12R, G12S, and G12V). In conclusion solid-phase PCR, combined with dual-color hybridization, allows mutation analysis in a shorter time span and is more suitable for automation.
AB - In a previous study we developed a highly sensitive DNA microarray for the detection of common KRAS oncogenic mutations, which has been proven to be highly specific in assigning the correct genotype without any enrichment strategy even in the presence of minority mutated alleles. However, in this approach, the need of a spotter for the deposition of the purified PCR products on the substrates and the purification step of the conventional PCR are serious drawbacks. To overcome these limitations we have introduced the solid-phase polymerase chain reaction (SP-PCR) to form the array of PCR products starting from the oligonucleotide primers. This work was possible thanks to the great thermal stability of the copoly (DMA-NAS-MAPS) coating which withstands PCR thermal cycling temperatures. As an example of the application of this platform we performed the analysis of six common mutations in the codon 12 of KRAS gene (G12A, G12C, G12D, G12R, G12S, and G12V). In conclusion solid-phase PCR, combined with dual-color hybridization, allows mutation analysis in a shorter time span and is more suitable for automation.
KW - DNA microarray
KW - Genotyping
KW - Polymer coated silicon slide
KW - Solid-phase PCR
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U2 - 10.1016/j.bios.2015.11.091
DO - 10.1016/j.bios.2015.11.091
M3 - Article
C2 - 26655175
AN - SCOPUS:84949429598
SN - 0956-5663
VL - 78
SP - 367
EP - 373
JO - Biosensors and Bioelectronics
JF - Biosensors and Bioelectronics
ER -