Nanopore detection of rhamnosylation in cyclic
peptides. (A) Schematic
representation of the cyclic peptides before and after the rhamnosylation
reaction. (B–D) Characteristic events (top), dwell time versus
excluded current (middle), and excluded current histogram (bottom)
of (B) 2.5 μM 11-mer_Pa_unmod, (C) 2.5 μM
11-mer_Pa_Rha, and (D) their 1:1 mixture in a final
concentration of 2.5 μM. The dotted lines indicate the approximate
ionic current levels of the unmodified (red) and rhamnosylated (green)
peptide. The locations of event cluster [1] and cluster
[2] are highlighted in red and yellow, respectively.
Measurements in 3 M LiCl and 50 mM citric acid buffered to pH 3.8
under an applied voltage of −50 mV. Data were recorded at 50
kHz sampling frequency, with a 10 kHz Bessel filter.