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Review

Duplex DNA Capture

by
Vadim V. Demidov
1,
Nikolay O. Bukanov
2 and
Maxim D. Frank-Kamenetskii
1
1
Boston University, 36 Cummington Street, Boston, MA 02215, USA
2
Genzyme Genetics, 1 Mountain Road, Framingham, MA 01701-9322, USA
Curr. Issues Mol. Biol. 2000, 2(1), 31-35; https://doi.org/10.21775/cimb.002.031
Submission received: 10 September 1999 / Revised: 19 November 1999 / Accepted: 5 December 1999 / Published: 1 January 2000

Abstract

This article describes the sequence-specific isolation and purification of intact double-stranded DNA (dsDNA) by oligonucleotide/PNA-assisted affinity capture (OPAC). The OPAC assay is based on selective tagging of a DNA duplex by biotinylated oligodeoxyribonucleotide (ODN) through formation of a so-called PD-loop. The PD-loop is assembled with the aid of a pair of PNA "openers", which allow sequence-specific targeting with a Watson-Crick complementary ODN probe in the exposed region of the dsDNA. The protocol involves three steps. First, two cationic bis-PNAs locally pry the DNA duplex apart at a predetermined site. Then, the exposed DNA single strand is targeted by a complementary biotinylated ODN to selectively form a stable PD-loop complex. Finally, the capture of dsDNA is performed using streptavidin covered magnetic beads. The OPAC procedure has many advantages in the isolation of highly purified native DNA over other affinity capture and amplification techniques.

Share and Cite

MDPI and ACS Style

Demidov, V.V.; Bukanov, N.O.; Frank-Kamenetskii, M.D. Duplex DNA Capture. Curr. Issues Mol. Biol. 2000, 2, 31-35. https://doi.org/10.21775/cimb.002.031

AMA Style

Demidov VV, Bukanov NO, Frank-Kamenetskii MD. Duplex DNA Capture. Current Issues in Molecular Biology. 2000; 2(1):31-35. https://doi.org/10.21775/cimb.002.031

Chicago/Turabian Style

Demidov, Vadim V., Nikolay O. Bukanov, and Maxim D. Frank-Kamenetskii. 2000. "Duplex DNA Capture" Current Issues in Molecular Biology 2, no. 1: 31-35. https://doi.org/10.21775/cimb.002.031

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