Abstract
ABSTRACTSugars are essential sources of energy and carbon, and also function as key signaling molecules in plants. Sugar Transport Proteins (STP) are proton-coupled symporters, solely responsible for uptake of glucose from the apoplastic compartment into cells in all plant tissues. They are integral to organ development in symplastically isolated tissues such as seeds, pollen and fruit. Additionally, STPs play a significant role in plant responses to both environmental stressors such as dehydration, and prevalent fungal infections like rust and mildew. Here, we present two high-resolution crystal structures of the outward-occluded and inward-open conformations of Arabidopsis thaliana STP10 with glucose and protons bound. The two structures describe key states in the STP transport cycle. Together with in vivo biochemical analysis and Molecular Dynamics simulations they pinpoint structural elements that explain how STPs exhibit high affinity for sugar binding on the extracellular side and how it is considerably lowered on the intracellular side to facilitate substrate release. These structural elements, conserved in all STPs across plant species, clarify the basis of proton-to-glucose coupling, essential for symport. The results advance our understanding of a key molecular mechanism behind plant organ development, and sets the stage for novel bioengineering strategies in crops that could target seeds, fruits and plant resistance to fungal infections.
Publisher
Cold Spring Harbor Laboratory
Cited by
2 articles.
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