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. 2021 Jul 24;12(35):11692–11702. doi: 10.1039/d1sc02715h

Fig. 4. K16-1 and K16-1c function as structure-switching aptamer sensors and are specific to kanamycin A. (a) Secondary structure of K16-1 with (left) and without (right) the 9 nt capture strand calculated using NUPACK. The K16-1c truncation is highlighted in purple with (left) and without (right) the 9 nt capture strand calculated using NUPACK. (b) Capture strand displacement as a function of kanamycin A concentration with 100 nM K16-1 and 500 nM K16-1c with 100 nM and 125 nM 9 nt capture strand, respectively. Samples resulting in negative displacement were denoted 0% displacement. Error bars denote standard error (n = 9). (c) Displacement of K16-1 (solid) and K16-1c (dashed) biosensors with 1 mM kanamycin A, kanamycin B, streptomycin, or tobramycin. Error bars denote standard error (n = 3).

Fig. 4