An engineered disulfide bridge traps and validates an outward‐facing conformation in a bile acid transporter. Issue 1 (6th January 2021)

• Record Type: Journal Article
• Authors: Wang, Xiaodong; Lyu, Ying; Ji, Yujia; Sun, Ziyi; Zhou, Xiaoming
• Is Part Of: Acta crystallographica. Volume 77:Issue 1(2021)
• Page Start: 108
• Page End: 116
• Publication Date: 2021-01-06
• Subjects: ASBT structure -- bile acid transporter -- disulfide bridge -- outward‐facing conformation -- binding affinity; X-ray crystallography -- Periodicals; Crystallography -- Periodicals; Molecular biology -- Periodicals; Molecular structure -- Periodicals; Biomolecules -- Structure -- Periodicals; Cytology -- Periodicals; Biomolecules -- Structure; Crystallography; Cytology; Molecular biology; Molecular structure; X-ray crystallography; Periodicals; 548
• DOI: 10.1107/S205979832001517X
• Languages: English
• ISSNs: 2059-7983

Abstract

Abstract : An engineered disulfide bridge traps and validates an outward‐facing conformation in a bile acid transporter from Yersinia frederiksenii . Abstract : Apical sodium‐dependent bile acid transporter (ASBT) mediates the uptake of bile acids from the ileum lumen into enterocytes and presents a potential target for the treatment of several metabolic diseases, including type 2 diabetes. It has been proposed that the underlying mechanism for transport by ASBT is an elevator‐style alternating‐access model, which was deduced mainly by comparing high‐resolution structures of two bacterial ASBT homologs (ASBTNM from Neisseria meningitides and ASBTYf from Yersinia frederiksenii ) in different conformations. However, one important issue is that the only outward‐facing structure (PDB entry 4n7x ) was obtained with an Na + ‐binding site mutant of ASBTYf, which severely cripples its transport function, and therefore the physiological relevance of the conformation in PDB entry 4n7x requires further careful evaluation. Here, another crystal structure is reported of ASBTYf that was captured in a state closely resembling the conformation in PDB entry 4n7x using an engineered disulfide bridge. The introduced cysteine mutations avoided any proposed Na + ‐ or substrate‐binding residues, and the resulting mutant retained both structural and functional integrity and behaved similarly to wild‐type ASBTYf . These data support the hypothesis that the PDB entry 4n7x ‐like structure represents a functional outward‐facing conformation of ASBTYf in its transport cycle.