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A DNA sieving matrix with thermally tunable mesh size
Author(s) -
Kan Cheuk Wai,
Barron Annelise E.
Publication year - 2003
Publication title -
electrophoresis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.666
H-Index - 158
eISSN - 1522-2683
pISSN - 0173-0835
DOI - 10.1002/elps.200390031
Subject(s) - matrix (chemical analysis) , dna , materials science , chemistry , nanotechnology , chromatography , biochemistry
We present a “proof‐of‐concept” study showing that a blend of thermo‐responsive and nonthermo‐responsive polymers can be used to create a DNA sieving matrix with a thermally tunable mesh size, or “dynamic porosity”. Various blends of two well‐studied sieving polymers for CE, including hydroxypropylcellulose (HPC), a thermo‐responsive polymer, and hydroxyethylcellulose (HEC), a nonthermo‐responsive polymer, were used to separate a double‐stranded DNA restriction digest (X174‐ Hae III). HPC exhibits a volume‐phase transition in aqueous solution which results in a collapse in polymer coil volume at ∼ 39°C. Utilizing a blend of HPC and HEC in a ratio of 1:5 by weight, we investigated the effects of changing mesh size on DNA separation, as controlled by temperature. High‐resolution DNA separations were obtained with the blended matrix at temperatures ranging from 25°C to 38°C. We evaluated changes in the selectivity of DNA separation with increasing temperature for certain pairs of small and large fragments. A pure HEC (nonthermo‐responsive) matrix was used over the same temperature range as a negative control. In the blended matrix, we observe a maximum in selectivity at ∼ 31°C for small DNA, while a significant increase in the selectivity of large‐DNA separation occurs at ∼ 36°C as the polymer mesh “opens”. We also demonstrate, through a temperature ramping experiment, that this matrix can be utilized to obtain high‐resolution separation of both small and large DNA fragments simultaneously in a single CE run. Blended polymer matrices with “dynamic porosity” have the potential to provide enhanced genomic analysis by capillary array or microchip electrophoresis in microfluidic devices with advanced temperature control.