Ionic and electrical gradients across cell and organelle membranes are created by pumps, whose correct functioning is essential to all biological and biomedical processes. Dysfunctional membrane proteins of this kind underlie many cardiac, neurological and digestive diseases, and they have been prominent targets of pharmaceutical intervention. We will study and describe proton transfer mechanisms in a newly discovered family of proton pumps that deviate from those in a model system employed earlier to generate general principles for active ion transport.
The aims of this proposal focus on the functional implications of our recently reported x-ray diffraction structure of xanthorhodopsin. We expect to uncover novel means of proton transfer in proteins, with insights into how energy input is used to move protons uphill, across the membrane. We hope that the findings will enrich the general field of membrane proteins, and that of transport proteins in particular. We will explore the consequences of three main differences from the x-ray structure of bacteriorhodopsin that we had reported earlier. a) The critical proton transfer, which in these proteins drives the transport, is from the retinal Schiff base to an aspartate connected via a water molecule at the active site. We now know that the proton acceptor can be also an aspartate-histidine complex with very likely shared protons. b) Release of protons to the bulk can be via an extended hydrogen-bonded network of polar residues and bound water, but now we know that an alternative exists that utilizes a deep cleft that extends into the proteins. c) Uptake of protons and reprotonation of the Schiff base by an internal acidic residue is via a transient chain of water molecules that spans an otherwise hydrophobic domain, during the transport cycle. We now know that this domain may contain water molecules that connect the proton donor to the Schiff base region. The experimental approaches to uncover the changed functions include the battery of methods we and our collaborators had developed over the past decades: construction of site-specific mutants expressed in E. coli, static and transient optical spectroscopy (absorption and fluorescence), site-specific spin labeling, Fourier Transform Infrared spectroscopy, crystallization and x-ray diffraction, and solution NMR.

Public Health Relevance

Life and health depend on maintaining the correct ionic balance between the interior of cells and their surroundings. The proposed work will contribute to the fundamental understanding of how pumps transport ions like protons across cell membranes. It will take advantage of novel features in a newly discovered family of pumps, and extend the range of possible mechanistic elements that add up to the translocation of the ion in these membrane devices.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM029498-32
Application #
8325065
Study Section
Biochemistry and Biophysics of Membranes Study Section (BBM)
Program Officer
Chin, Jean
Project Start
1981-07-01
Project End
2014-08-31
Budget Start
2012-09-01
Budget End
2013-08-31
Support Year
32
Fiscal Year
2012
Total Cost
$529,521
Indirect Cost
$183,429
Name
University of California Irvine
Department
Physiology
Type
Schools of Medicine
DUNS #
046705849
City
Irvine
State
CA
Country
United States
Zip Code
92697
McIsaac, R Scott; Engqvist, Martin K M; Wannier, Timothy et al. (2014) Directed evolution of a far-red fluorescent rhodopsin. Proc Natl Acad Sci U S A 111:13034-9
Dioumaev, Andrei K; Petrovskaya, Lada E; Wang, Jennifer M et al. (2013) Photocycle of Exiguobacterium sibiricum rhodopsin characterized by low-temperature trapping in the IR and time-resolved studies in the visible. J Phys Chem B 117:7235-53
Balashov, Sergei P; Petrovskaya, Lada E; Imasheva, Eleonora S et al. (2013) Breaking the carboxyl rule: lysine 96 facilitates reprotonation of the Schiff base in the photocycle of a retinal protein from Exiguobacterium sibiricum. J Biol Chem 288:21254-65
Slouf, Vaclav; Balashov, Sergei P; Lanyi, Janos K et al. (2011) Carotenoid response to retinal excitation and photoisomerization dynamics in xanthorhodopsin. Chem Phys Lett 516:96-101
Imasheva, Eleonora S; Balashov, Sergei P; Wang, Jennifer M et al. (2011) Removal and reconstitution of the carotenoid antenna of xanthorhodopsin. J Membr Biol 239:95-104
Balashov, Sergei P; Imasheva, Eleonora S; Choi, Ah Reum et al. (2010) Reconstitution of gloeobacter rhodopsin with echinenone: role of the 4-keto group. Biochemistry 49:9792-9
Polivka, Tomas; Balashov, Sergei P; Chabera, Pavel et al. (2009) Femtosecond carotenoid to retinal energy transfer in xanthorhodopsin. Biophys J 96:2268-77
Chen, Deliang; Lanyi, Janos K (2009) Structural changes in the N and N'states of the bacteriorhodopsin photocycle. Biophys J 96:2779-88
Imasheva, Eleonora S; Balashov, Sergei P; Wang, Jennifer M et al. (2008) Chromophore interaction in xanthorhodopsin--retinal dependence of salinixanthin binding. Photochem Photobiol 84:977-84
Balashov, Sergei P; Imasheva, Eleonora S; Wang, Jennifer M et al. (2008) Excitation energy-transfer and the relative orientation of retinal and carotenoid in xanthorhodopsin. Biophys J 95:2402-14

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