Kusakizako Tsukasa, Tanaka Yoshiki, Hipolito Christopher J, Suga Hiroaki, Nureki Osamu
Department of Biological Sciences, Graduate School of Science, The University of Tokyo, 2-11-16 Yayoi, Bunkyo-ku, Tokyo, 113-0032, Japan.
Department of Systems Biology, Graduate School of Biological Sciences, Nara Institute of Science and Technology, 8916-5, Takayama-cho, Ikoma, Nara, 630-0192, Japan.
Methods Mol Biol. 2018;1700:37-57. doi: 10.1007/978-1-4939-7454-2_3.
Multidrug exporters expressed in pathogens efflux substrate drugs such as antibiotics, and thus, the development of inhibitors against them has eagerly been anticipated. Furthermore, the crystal structures of multidrug exporters with their inhibitors provide novel insights into the inhibitory mechanism and the development of more specific and effective inhibitors. We previously reported the complex structures of the Multidrug And Toxic compound Extrusion (MATE)-type multidrug exporter with the macrocyclic peptides, which inhibit the efflux of substrates by the MATE-type multidrug exporter (Tanaka et al., Nature 496:247-251, 2013). In this chapter, we describe methodologies of the screening and synthesis of macrocyclic peptides as inhibitors, as well as the purification, crystallization, and structure determination of the complexes of the MATE-type multidrug exporter with its inhibitors.
病原体中表达的多药外排泵可外排诸如抗生素等底物药物,因此,人们迫切期待开发针对它们的抑制剂。此外,多药外排泵与其抑制剂的晶体结构为抑制机制以及开发更具特异性和有效性的抑制剂提供了新的见解。我们之前报道了多药与毒性化合物外排(MATE)型多药外排泵与大环肽的复合物结构,这些大环肽可抑制MATE型多药外排泵对底物的外排(Tanaka等人,《自然》496:247 - 251,2013)。在本章中,我们描述了作为抑制剂的大环肽的筛选与合成方法,以及MATE型多药外排泵与其抑制剂复合物的纯化、结晶和结构测定方法。