SWEET Family Transporters Act as Water-Conducting Carrier Proteins in Plants

Dedicated water channels are involved in the facilitated diffusion of water molecules across cell membranes in plants. Transporter proteins are also known to transport water molecules along with substrates; however, the molecular mechanism of water permeation is not well understood in plant transporters. Here, we show that plant sugar transporters from the SWEET (<b>s</b>ugar <b>w</b>ill <b>e</b>ventually be <b>e</b>xported <b>t</b>ransporter) family act as water-conducting carrier proteins via a variety of passive and active mechanisms that allow the diffusion of water molecules from one side of the membrane to the other. This study provides a molecular perspective on how plant membrane transporters act as water carrier proteins, a topic that has not been extensively explored in the literature. Water permeation in membrane transporters could occur via four distinct mechanisms, which form our hypothesis for water transport in SWEETs. These hypotheses are tested using molecular dynamics simulations of the outward-facing, occluded, and inward-facing states of AtSWEET1 to identify the water permeation pathways and the flux associated with them. The hydrophobic gates at the center of the transport tunnel act as barriers that restrict water permeation. We have performed in silico single and double mutations of the hydrophobic gate residues to examine the changes in water conductivity. Surprisingly, the double mutant allows water permeation to the intracellular half of the membrane and forms a continuous water channel. These computational results are validated by experimentally examining the transport of hydrogen peroxide molecules by the AtSWEET family of transporters. We have also shown that the transport of hydrogen peroxide follows a mechanism similar to that of water transport in AtSWEET1. Finally, we conclude that similar water-conduction states are also present in other SWEETs due to the high degree of sequence and structural conservation exhibited by this transporter family.

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Publication Details

Journal
Journal of Chemical Information and Modeling
Published
2025-03-29
DOI
https://doi.org/10.1021/acs.jcim.5c00110
Citations
2
Primary Topic
Plant nutrient uptake and metabolism
Type
article
Field-Weighted Citation Impact
3.50
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article

SWEET Family Transporters Act as Water-Conducting Carrier Proteins in Plants

Balaji Selvam, Arnav Paul, Diwakar Shukla, Li‐Qing Chen et al.
2 citations
Journal of Chemical Information and Modeling
Plant nutrient uptake and metabolism
3.50
article

SWEET Family Transporters Act as Water-Conducting Carrier Proteins in Plants

Balaji Selvam, Arnav Paul, Diwakar Shukla, Li‐Qing Chen, Ya‐Chi Yu
article en
2 citations

Abstract

Dedicated water channels are involved in the facilitated diffusion of water molecules across cell membranes in plants. Transporter proteins are also known to transport water molecules along with substrates; however, the molecular mechanism of water permeation is not well understood in plant transporters. Here, we show that plant sugar transporters from the SWEET (<b>s</b>ugar <b>w</b>ill <b>e</b>ventually be <b>e</b>xported <b>t</b>ransporter) family act as water-conducting carrier proteins via a variety of passive and active mechanisms that allow the diffusion of water molecules from one side of the membrane to the other. This study provides a molecular perspective on how plant membrane transporters act as water carrier proteins, a topic that has not been extensively explored in the literature. Water permeation in membrane transporters could occur via four distinct mechanisms, which form our hypothesis for water transport in SWEETs. These hypotheses are tested using molecular dynamics simulations of the outward-facing, occluded, and inward-facing states of AtSWEET1 to identify the water permeation pathways and the flux associated with them. The hydrophobic gates at the center of the transport tunnel act as barriers that restrict water permeation. We have performed in silico single and double mutations of the hydrophobic gate residues to examine the changes in water conductivity. Surprisingly, the double mutant allows water permeation to the intracellular half of the membrane and forms a continuous water channel. These computational results are validated by experimentally examining the transport of hydrogen peroxide molecules by the AtSWEET family of transporters. We have also shown that the transport of hydrogen peroxide follows a mechanism similar to that of water transport in AtSWEET1. Finally, we conclude that similar water-conduction states are also present in other SWEETs due to the high degree of sequence and structural conservation exhibited by this transporter family.

Journal of Chemical Information and ModelingVol. 65(7)
University of Illinois Urbana-Champaign (US)
Clean water and sanitation
Openalex Percentile: Top 9%
Plant nutrient uptake and metabolism
3.50
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