A Tandem Cell for Nanopore-based DNA Sequencing with Exonuclease
Abstract
A tandem cell is proposed for DNA sequencing in which an exonuclease enzyme cleaves bases (mononucleotides) from a strand of DNA for identification inside a nanopore. It has two nanopores and three compartments with the structure [cis1, upstream nanopore (UNP), trans1=cis2, downstream nanopore (DNP), trans2]. The exonuclease is attached to the exit side of UNP in trans1/cis2. A cleaved base cannot regress into cis1 because of the remaining DNA strand in UNP. A profiled electric field over DNP with positive and negative components slows down base translocation through DNP. The proposed structure is modeled with a Fokker-Planck equation and a piecewise solution presented. Results from the model indicate that with probability approaching 1 bases enter DNP in their natural order, are detected without any loss, and do not regress into DNP after progressing into trans2. Sequencing efficiency with a tandem cell would then be determined solely by the level of discrimination among the base types inside DNP.
Keywords
Cite
@article{arxiv.1408.4480,
title = {A Tandem Cell for Nanopore-based DNA Sequencing with Exonuclease},
author = {G. Sampath},
journal= {arXiv preprint arXiv:1408.4480},
year = {2014}
}
Comments
14 pages, 8 figures