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A novel pathogen detection system based on high-resolution CE-SSCP using a triblock copolymer matrix

Cited 25 time in Web of Science Cited 26 time in Scopus
Authors

Shin, Gi Won; Hwang, Hee Sung; Seo, Sang Woo; Oh, Mi-Hwa; Ryu, Chang Y.; Salvo, Charles J.; Feldman, Shaina; Doh, Junsang; Jung, Gyoo Yeol

Issue Date
2010-06
Publisher
Wiley-VCH Verlag
Citation
Journal of Separation Science, Vol.33 No.11, pp.1639-1643
Abstract
Although CE-SSCP analysis combined with 16S ribosomal RNA gene-specific PCR has enormous potential as a simple and versatile pathogen detection technique, low resolution of CE-SSCP causes the limited application. Among the experimental conditions affecting the resolution, the polymer matrix is considered to be most critical to improve the resolution of CE-SSCP analysis. However, due to the peak broadening caused by the interaction between hydrophobic moiety of polymer matrices and DNA, conventional polymer matrices are not ideal for CE-SSCP analysis. A poly(ethyleneoxide)-poly(propyleneoxide)-poly(ethyleneoxide) (PEO-PPO-PEO) triblock copolymer, with dynamic coating ability and a propensity to form micelles to minimize exposure of hydrophobic PPO block to DNA, can be an alternative matrix. In this study, we examined the resolution of CE-SSCP analysis using the PEO-PPO-PEO triblock copolymer as the polymer matrix and four same-sized DNA fragments of similar sequence content. Among 48 commercially available PEO-PPO-PEO triblock copolymers, three were selected due to their transparency in the operable range of viscosity and PEO137PPO 43PEO137 exhibited the most effective separation. Significant improvement in resolution allowed discrimination of the similar sequences, thus greatly facilitated CE-SSCP analysis compared to the conventional polymer matrix. The results indicate that PEO-PPO-PEO triblock copolymer may serve as an ideal matrix for high-resolution CE-SSCP analysis. © 2010 Wiley-VCH Verlag GmbH & Co. KGaA.
ISSN
1615-9306
URI
https://hdl.handle.net/10371/203231
DOI
https://doi.org/10.1002/jssc.200900871
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  • Department of Materials Science & Engineering
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