Enzyme-less DNA base identification by chemical stepping in a nanopore

The stepwise movement of a single biopolymer strand through a nanoscopic detector for the sequential identification of its building blocks offers a universal means for single-molecule sequencing. This principle has been implemented in portable sequencers that use enzymes to move DNA or RNA through h...

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Main Authors: Qing, Y, Bayley, H
Format: Journal article
Language:English
Published: American Chemical Society 2021
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author Qing, Y
Bayley, H
author_facet Qing, Y
Bayley, H
author_sort Qing, Y
collection OXFORD
description The stepwise movement of a single biopolymer strand through a nanoscopic detector for the sequential identification of its building blocks offers a universal means for single-molecule sequencing. This principle has been implemented in portable sequencers that use enzymes to move DNA or RNA through hundreds of individual nanopore detectors positioned in an array. Nevertheless, its application to the sequencing of other biopolymers, including polypeptides and polysaccharides, has not progressed because suitable enzymes are lacking. Recently, we devised a purely chemical means to move molecules processively in steps comparable to the repeat distances in biopolymers. Here, with this chemical approach, we demonstrate sequential nucleobase identification during DNA translocation through a nanopore. Further, the relative location of a guanine modification with a chemotherapeutic platinum derivative is pinpointed with single-base resolution. After further development, chemical translocation might replace stepping by enzymes for highly parallel single-molecule biopolymer sequencing.
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spelling oxford-uuid:9adb2aae-d925-484b-affb-9345a842a54a2022-10-20T10:08:27ZEnzyme-less DNA base identification by chemical stepping in a nanoporeJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:9adb2aae-d925-484b-affb-9345a842a54aEnglishSymplectic ElementsAmerican Chemical Society2021Qing, YBayley, HThe stepwise movement of a single biopolymer strand through a nanoscopic detector for the sequential identification of its building blocks offers a universal means for single-molecule sequencing. This principle has been implemented in portable sequencers that use enzymes to move DNA or RNA through hundreds of individual nanopore detectors positioned in an array. Nevertheless, its application to the sequencing of other biopolymers, including polypeptides and polysaccharides, has not progressed because suitable enzymes are lacking. Recently, we devised a purely chemical means to move molecules processively in steps comparable to the repeat distances in biopolymers. Here, with this chemical approach, we demonstrate sequential nucleobase identification during DNA translocation through a nanopore. Further, the relative location of a guanine modification with a chemotherapeutic platinum derivative is pinpointed with single-base resolution. After further development, chemical translocation might replace stepping by enzymes for highly parallel single-molecule biopolymer sequencing.
spellingShingle Qing, Y
Bayley, H
Enzyme-less DNA base identification by chemical stepping in a nanopore
title Enzyme-less DNA base identification by chemical stepping in a nanopore
title_full Enzyme-less DNA base identification by chemical stepping in a nanopore
title_fullStr Enzyme-less DNA base identification by chemical stepping in a nanopore
title_full_unstemmed Enzyme-less DNA base identification by chemical stepping in a nanopore
title_short Enzyme-less DNA base identification by chemical stepping in a nanopore
title_sort enzyme less dna base identification by chemical stepping in a nanopore
work_keys_str_mv AT qingy enzymelessdnabaseidentificationbychemicalsteppinginananopore
AT bayleyh enzymelessdnabaseidentificationbychemicalsteppinginananopore