Engineering and Physical Sciences Research Council
EP/L000253/1
英国
Wellcome Trust
209194
英国
Wellcome Trust
100298
英国
Wellcome Trust
219531
英国
Wellcome Trust
215519
英国
Wellcome Trust
219531
英国
Medical Research Council (MRC, United Kingdom)
MR/M011984/1
英国
Medical Research Council (MRC, United Kingdom)
MR/S021043/1
英国
Wellcome Trust
203741
英国
引用
ジャーナル: Sci Adv / 年: 2021 タイトル: Cryo-EM structure of PepT2 reveals structural basis for proton-coupled peptide and prodrug transport in mammals. 著者: Joanne L Parker / Justin C Deme / Zhiyi Wu / Gabriel Kuteyi / Jiandong Huo / Raymond J Owens / Philip C Biggin / Susan M Lea / Simon Newstead / 要旨: The SLC15 family of proton-coupled solute carriers PepT1 and PepT2 play a central role in human physiology as the principal route for acquiring and retaining dietary nitrogen. A remarkable feature of ...The SLC15 family of proton-coupled solute carriers PepT1 and PepT2 play a central role in human physiology as the principal route for acquiring and retaining dietary nitrogen. A remarkable feature of the SLC15 family is their extreme substrate promiscuity, which has enabled the targeting of these transporters for the improvement of oral bioavailability for several prodrug molecules. Although recent structural and biochemical studies on bacterial homologs have identified conserved sites of proton and peptide binding, the mechanism of peptide capture and ligand promiscuity remains unclear for mammalian family members. Here, we present the cryo-electron microscopy structure of the outward open conformation of the rat peptide transporter PepT2 in complex with an inhibitory nanobody. Our structure, combined with molecular dynamics simulations and biochemical and cell-based assays, establishes a framework for understanding peptide and prodrug recognition within this pharmaceutically important transporter family.