) nanopores assisted by a circular single-stranded DNA (CssDNA) frame. This frame comprises an aptamer designed to specifically capture αS oligomers. The αS oligomers can be identified and classified into four different species, from dimers to heptamers, by analyzing the events based on particular subpeaks produced by the complexes of the CssDNA frame incubated with αS monomers for 2 h and translocation through the nanopores. CssDNA frame also captured αS oligomers with 0.5 h incubation, and the detected oligomers are primarily dimers. Finally, the selectivity of CssDNA frame is confirmed by detecting and analyzing the complexes formed by the CssDNA frame incubated with β-lactoglobulin, Aβ1-42 and tau proteins. The developed approach is a promising alternative for achieving the quantitative analysis of αS oligomers at single-molecule levels.
Heng et al. (Wed,) studied this question.