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. 2019 Sep 19;13(12):13668–13676. doi: 10.1021/acsnano.9b05156

Figure 2.

Figure 2

Peptide labeled at different positions through FraC. From left to right: Schematic, current traces, and relative blockade histograms for unlabeled peptide (a) and for fluorescein-labeled peptide at positions C11 (b), C15 (c), and C20 (d). All labeled peptide samples were HPLC purified and verified using mass spectrometry. Measurements were done in a buffer containing 1 M NaCl, 10 mM Tris, and 1 mM EDTA at pH 7.5. Peptides were added to the cis compartment and measured at −90 mV.