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. Author manuscript; available in PMC: 2017 Jun 7.
Published in final edited form as: Structure. 2016 May 5;24(6):956–964. doi: 10.1016/j.str.2016.04.003

Figure 1. bcMalT is a maltose transporter.

Figure 1

a. Competitive binding to full-length bcMalT in LDAO between [3H]maltose and unlabeled maltose. b. Binding of [3H]maltose to full-length bcMalT solubilized in either LDAO or DM. c. Competitive binding to full-length bcMalT in LDAO between [3H]maltose and 500 μM of the indicated unlabeled sugars, measured by SPA. d. Uptake of [3H]maltose into proteoliposomes containing full-length bcMalT (black squares) or control liposomes without protein (white circles). Error bars are standard deviations of three technical replicates. e. Verification of [3H]maltose uptake by comparing accumulation in proteoliposomes incorporating full-length bcMalT or control liposomes without protein in the presence or absence of 5 mM LDAO.