Structure of a eukaryotic SWEET transporter in a homotrimeric complex

Tao, Yuyong; Cheung, Lily S.; Li, Shuo; Eom, Joon-Seob; Chen, Li-Qing; Xu, Yan; Perry, Kay; Frommer, Wolf B.; Feng, Liang

doi:10.1038/nature15391

Title: Structure of a eukaryotic SWEET transporter in a homotrimeric complex

Journal Article · Mon Oct 19 00:00:00 EDT 2015 · Nature (London)

DOI:https://doi.org/10.1038/nature15391· OSTI ID:1226370

Tao, Yuyong ^[1]; Cheung, Lily S. ^[2]; Li, Shuo ^[3]; Eom, Joon-Seob ^[2]; Chen, Li-Qing ^[2]; Xu, Yan ^[1]; Perry, Kay ^[4]; Frommer, Wolf B. ^[2]; Feng, Liang ^[1]

Stanford Univ., CA (United States). School of Medicine. Dept. of Molecular and Cellular Physiology
Carnegie Inst. of Science, Stanford, CA (United States). Dept. of Plant Biology
Stanford Univ., CA (United States). School of Medicine. Dept. of Molecular and Cellular Physiology; Sichuan Univ., Chengdu (China). College of Life Sciences. Key Lab. of Bio-Resource and Eco-Environment of Ministry of Education. Center of Growth, Metabolism and Aging
Argonne National Lab. (ANL), Argonne, IL (United States). NE-CAT. Dept. of Chemistry and Chemical Biology

Eukaryotes rely on efficient distribution of energy and carbon skeletons between organs in the form of sugars. Glucose in animals and sucrose in plants serve as the dominant distribution forms. Cellular sugar uptake and release require vesicular and/or plasma membrane transport proteins. Humans and plants use proteins from three superfamilies for sugar translocation: the major facilitator superfamily (MFS), the sodium solute symporter family (SSF; only in the animal kingdom), and SWEETs. SWEETs carry mono- and disaccharides across vacuolar or plasma membranes. Plant SWEETs play key roles in sugar translocation between compartments, cells, and organs, notably in nectar secretion, phloem loading for long distance translocation, pollen nutrition, and seed filling. Plant SWEETs cause pathogen susceptibility possibly by sugar leakage from infected cells. The vacuolar Arabidopsis thaliana AtSWEET2 sequesters sugars in root vacuoles; loss-of-function mutants show increased susceptibility to Pythium infection. In this paper, we show that its orthologue, the vacuolar glucose transporter OsSWEET2b from rice (Oryza sativa), consists of an asymmetrical pair of triple-helix bundles, connected by an inversion linker transmembrane helix (TM4) to create the translocation pathway. Structural and biochemical analyses show OsSWEET2b in an apparent inward (cytosolic) open state forming homomeric trimers. TM4 tightly interacts with the first triple-helix bundle within a protomer and mediates key contacts among protomers. Structure-guided mutagenesis of the close paralogue SWEET1 from Arabidopsis identified key residues in substrate translocation and protomer crosstalk. Finally, insights into the structure–function relationship of SWEETs are valuable for understanding the transport mechanism of eukaryotic SWEETs and may be useful for engineering sugar flux.

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Research Organization:: Stanford Univ., CA (United States); Carnegie Inst. of Science, Stanford, CA (United States)

Sponsoring Organization:: USDOE Office of Science (SC), Basic Energy Sciences (BES); National Science Foundation (NSF); National Inst. of Health (NIH) (United States); Stanford Univ. (United States); Harold and Leila Y. Mathers Charitable Foundation (United States); Alfred P. Sloan Foundation (United States); National Natural Science Foundation of China (NSFC)

Contributing Organization:: Sichuan Univ., Chengdu (China); Argonne National Lab. (ANL), Argonne, IL (United States)

Grant/Contract Number:: FG02-04ER15542; AC02-06CH11357; IOS-1258018; 1401855; P41 GM103403; 31300618

OSTI ID:: 1226370

Journal Information:: Nature (London), Vol. 527, Issue 7577; ISSN 0028-0836

Publisher:: Nature Publishing GroupCopyright Statement

Country of Publication:: United States

Language:: ENGLISH

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Cited by: 119 works

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