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Updated: Apr 26, 2026

Quantitative, Real-time Analysis of Base Excision Repair Activity in Cell Lysates Utilizing Lesion-specific Molecular Beacons
Published on: August 6, 2012
Genotyping single nucleotide polymorphisms using different molecular beacon multiplexed within a suspended core
Linh Viet Nguyen1, Sara Giannetti2, Stephen Warren-Smith3
1Institute for Photonics and Advanced Sensing (IPAS) and The ARC Centre for Nanoscale Biophotonics, The University of Adelaide, Adelaide 5005, Australia. vietlinh.nguyen@adelaide.edu.au.
Abstract:
We report a novel approach to genotyping single nucleotide polymorphisms (SNPs) using molecular beacons in conjunction with a suspended core optical fiber (SCF). Target DNA sequences corresponding to the wild- or mutant-type have been accurately recognized by immobilizing two different molecular beacons on the core of a SCF. The two molecular beacons differ by one base in the loop-probe and utilize different fluorescent indicators. Single-color fluorescence enhancement was obtained when the immobilized SCFs were filled with a solution containing either wild-type or mutant-type sequence (homozygous sample), while filling the immobilized SCF with solution containing both wild- and mutant-type sequences resulted in dual-color fluorescence enhancement, indicating a heterozygous sample. The genotyping was realized amplification-free and with ultra low-volume for the required DNA solution (nano-liter). This is, to our knowledge, the first genotyping device based on the combination of optical fiber and molecular beacons.

