Our goal is to understand the mechanisms of intestinal ion, nutrient and water transport. Our approach is to express the brush border Na+/glucose contransporter (SGLT1) and fructose transporter (GLUT5) in Xenopus laevis oocytes, and to use a combination of molecular, biochemical and biophysical techniques to study glucose, fructose and water transport. We have demonstrated that SGLT1 transports Na+, glucose and water in a fixed stoichiometry, 2Na+/1 glucose/250 water, and we have proposed that cotransport is due to ligand and voltage- induced conformation changes. A major specific aim is to determine the structural basis of these conformational changes. SGLT1 will be expressed at high levels in oocytes, > 10/11 copies per cell, extrinsic fluorescent probes will be attached to sugar and ion binding sites, and optical methods will be used to probe the structure, and distance between , the sites. These measurements will be made on SGLT1 in different conformations, and during fast (us) changes from one conformation to another. The current model for contransport will be tested by measuring the kinetics and ligand specificity of the transporter working backwards, and comparing the results with novel predictions. A critical thermodynamic test of water cotransport will be to measure the effect of osmotic gradients of the energetics of Na+/ sugar co transport. These experiments will provide novel kinetic and structural information about Na+/sugar/water cotransport. We will examine the oligomeric structure and kinetic mechanism of fructose transport by GLUT5 and determine the role of GLUT5 in water transport. Experiments will be carried out GLUT5 expressed in oocytes, where we will measure fructose transport kinetics using radioactive tracer uptakes, the density and structure of GLUT5 in the plasma membrane using freeze fracture electron microscopy, and partial reactions using voltage-jump experiments. This data will be used to construct a kinetic model for fructose transport. Water transport by GLUT5 in the presence and absence of fructose will be measured by an optical method, and the result will be normalized to the number GLUT5 molecules expressed in the plasma membrane this will allow us to determine the role of GLUT5 in water transport across the brush border membrane.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK019567-23
Application #
6177122
Study Section
General Medicine A Subcommittee 2 (GMA)
Program Officer
May, Michael K
Project Start
1976-12-01
Project End
2003-03-31
Budget Start
2000-04-01
Budget End
2001-03-31
Support Year
23
Fiscal Year
2000
Total Cost
$271,134
Indirect Cost
Name
University of California Los Angeles
Department
Physiology
Type
Schools of Medicine
DUNS #
119132785
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
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
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
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