Abstract Glucosinolates (GLSs) are sulfur-rich secondary metabolites characteristic of Brassicales and play central roles in plant defense. While the biosynthesis and long-distance allocation of GLSs have been extensively studied, the molecular principles underlying their membrane transport by Glucosinolate Transporters (GTRs) remain poorly understood. Here, we report cryogenic electron microscopy (cryo-EM) structures of Arabidopsis thaliana GTR1 (AtGTR1) in apo and substrate-bound states. Structures of AtGTR1 in complex with the glucobrassicin (3-indolylmethyl glucosinolate, I3M), were determined at two pH conditions, capturing the transporter in a conserved inward-open conformation. The structures reveal a central substrate-binding cavity formed at the interface of the N- and C-terminal domains. Structural analyses uncover a conserved recognition strategy in which AtGTR1 selectively engages the common glucosinolate scaffold while tolerating substantial variation in side chains, thereby explaining its polyspecificity. These findings establish a structural framework for GTRs and provide mechanistic insights that enable rational manipulation of GLSs allocation for crop improvement.
Nan et al. (Fri,) studied this question.