The goal of this project is to understand how sodium, glucose and water are transported across the brush border membrane of the small intestine by the Na+/glucose cotransporter (hSGLT1). This membrane transport protein is responsible for the absorption of 180 g of glucose and galactose and more than 4 liters of fluid per day. Oral Rehydration Therapy, credited with saving thousands of infants a day from infectious diarrhea, is based on the coupling of glucose, salt and water transport by SGLT1. It is postulated that hSGLT1 couples Na+ transport to glucose and water transport by a series of ordered ligand induced conformational changes. Evidence suggests that sodium binding produces a reorganization of four transmemembranes helices near the C-terminus of the protein that permits sugar binding and transport. In order to accommodate the large glycosides that are transported (20 x 12 x 7 Angstroms) and the 300 water molecules that are also transported during one turnover of the transporter, we predict extensive changes in transmembrane helical packing during the transport cycle. To test this hypothesis we will use cysteine scanning mutagenesis along with thiol reactive fluorescent probes to identify which helices move, the order in which they move, and the distances they move during partial reactions of the transport cycle. This will be accomplished by expressing the cysteine mutant transporters in Xenopus laevis oocytes, and the cysteine residues will be labeled with fluorescent thiol reagents. The oocytes will be placed on the stage of an epifluorescence microscope and voltage clamped. Simultaneous recordings of charge movement and fluorescence will be obtained as a function of membrane voltage and the ligand concentrations. We will also use double cysteine mutants and fluorescence and luminescence energy transfer (FRET & LRET) to measure the distance between the probes on the two cysteines and how far they move as the transporter is moved from one conformation to another. This information will enable us to map the changes in helical packing, including the order, time course and magnitude of the helical motion during the transport cycle, and determine if they account for the transport of glucose and water. The impact of the work ranges from a molecular understanding of oral rehydration therapy to how large class of membrane transport proteins work.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK019567-30
Application #
7217920
Study Section
General Medicine A Subcommittee 2 (GMA)
Program Officer
May, Michael K
Project Start
1976-12-01
Project End
2009-03-31
Budget Start
2007-04-01
Budget End
2009-03-31
Support Year
30
Fiscal Year
2007
Total Cost
$289,195
Indirect Cost
Name
University of California Los Angeles
Department
Physiology
Type
Schools of Medicine
DUNS #
092530369
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
Kepe, Vladimir; Scafoglio, Claudio; Liu, Jie et al. (2018) Positron emission tomography of sodium glucose cotransport activity in high grade astrocytomas. J Neurooncol 138:557-569
Paz, Aviv; Claxton, Derek P; Kumar, Jay Prakash et al. (2018) Conformational transitions of the sodium-dependent sugar transporter, vSGLT. Proc Natl Acad Sci U S A 115:E2742-E2751
Gorraitz, Edurne; Hirayama, Bruce A; Paz, Aviv et al. (2017) Active site voltage clamp fluorometry of the sodium glucose cotransporter hSGLT1. Proc Natl Acad Sci U S A 114:E9980-E9988
Ghezzi, Chiara; Yu, Amy S; Hirayama, Bruce A et al. (2017) Dapagliflozin Binds Specifically to Sodium-Glucose Cotransporter 2 in the Proximal Renal Tubule. J Am Soc Nephrol 28:802-810
Adelman, Joshua L; Ghezzi, Chiara; Bisignano, Paola et al. (2016) Stochastic steps in secondary active sugar transport. Proc Natl Acad Sci U S A 113:E3960-6
Sala-Rabanal, Monica; Hirayama, Bruce A; Ghezzi, Chiara et al. (2016) Revisiting the physiological roles of SGLTs and GLUTs using positron emission tomography in mice. J Physiol 594:4425-38
Zeuthen, Thomas; Gorraitz, Edurne; Her, Ka et al. (2016) Structural and functional significance of water permeation through cotransporters. Proc Natl Acad Sci U S A 113:E6887-E6894
Gallo, Linda A; Wright, Ernest M; Vallon, Volker (2015) Probing SGLT2 as a therapeutic target for diabetes: basic physiology and consequences. Diab Vasc Dis Res 12:78-89
Scafoglio, Claudio; Hirayama, Bruce A; Kepe, Vladimir et al. (2015) Functional expression of sodium-glucose transporters in cancer. Proc Natl Acad Sci U S A 112:E4111-9
Adelman, Joshua L; Sheng, Ying; Choe, Seungho et al. (2014) Structural determinants of water permeation through the sodium-galactose transporter vSGLT. Biophys J 106:1280-9

Showing the most recent 10 out of 115 publications