Zwama Martijn, Yamasaki Seiji, Nakashima Ryosuke, Sakurai Keisuke, Nishino Kunihiko, Yamaguchi Akihito
Laboratory of Cell Membrane Structural Biology, Institute of Scientific and Industrial Research, Osaka University, Ibaraki, Osaka, 567-0047, Japan.
Department of Biomolecular Science and Regulation, Institute of Scientific and Industrial Research, Osaka University, Ibaraki, Osaka, 567-0047, Japan.
Nat Commun. 2018 Jan 9;9(1):124. doi: 10.1038/s41467-017-02493-1.
AcrB is the major multidrug exporter in Escherichia coli. Although several substrate-entrances have been identified, the specificity of these various transport paths remains unclear. Here we present evidence for a substrate channel (channel 3) from the central cavity of the AcrB trimer, which is connected directly to the deep pocket without first passing the switch-loop and the proximal pocket . Planar aromatic cations, such as ethidium, prefer channel 3 to channels 1 and 2. The efflux through channel 3 increases by targeted mutations and is not in competition with the export of drugs such as minocycline and erythromycin through channels 1 and 2. A switch-loop mutant, in which the pathway from the proximal to the deep pocket is hindered, can export only channel 3-utilizing drugs. The usage of multiple entrances thus contributes to the recognition and transport of a wide range of drugs with different physicochemical properties.
AcrB是大肠杆菌中主要的多药外排泵。尽管已经确定了几个底物入口,但这些不同转运途径的特异性仍不清楚。在此,我们提供证据表明,存在一条从AcrB三聚体中央腔出发的底物通道(通道3),该通道直接连接到深口袋,而无需先经过开关环和近端口袋。平面芳香族阳离子,如乙锭,比起通道1和通道2,更倾向于通过通道3。通过通道3的外排通过靶向突变而增加,并且与米诺环素和红霉素等药物通过通道1和通道2的输出不存在竞争关系。一个开关环突变体,其中从近端口袋到深口袋的途径受阻,只能输出利用通道3的药物。因此,多个入口的使用有助于识别和转运具有不同物理化学性质的多种药物。