My laboratory is fascinated by four questions: How do membrane-binding domains interact with membranes to target signal transduction proteins to various subcellular compartments? How can pH-induced refolding on membranes of diphtheria toxin T-domain and colicins cause highly charged helices to cross lipid bilayers? How can short, highly basic """"""""Trojan"""""""" peptides - such as penetratin and HIV-TAT peptide - cross pure lipid vesicles unaided, as some claim? How do simple toxins and antimicrobial peptides permeabilize membranes? The shared theme of these challenging questions is mediation of biological function through direct physicochemical interactions of proteins with lipid bilayers, especially the bilayer interface: Subcellular specificity of signal transduction domains is expressed directly through interfacial interactions. Breaching of the lipid bilayer by diphtheria toxin, Trojan peptides, and antimicrobial peptides begins with interfacial interactions, which 'set up' the peptide-bilayer complex for protein insertion/translocation. The physical principles underlying these interactions also underlie membrane protein (MP) stability, and are the key to predicting 3D structure from sequence. Our unique capabilities for combined structural and thermodynamic studies of peptide-bilayer interactions have brought us to the threshold of significant new advances, not only in fundamental principles, but also in their application to challenging biological problems.
Our specific aims embrace the broad objectives of enlarging our understanding of basic physicochemical principles, developing new structural methods for thermally disordered membranes, and applying these principles and methods to important biological problems: (1) Clarify how hydrophobic and electrostatic interactions work together at membrane interfaces to mediate protein-lipid interactions. (2) Advance the development of a novel diffraction method - Molecular Dynamics/Absolute Scale (MoDAS) refinement- in order to gain dynamic structural images of peptides interacting at the atomic level with thermally disordered lipid bilayers. (3) Elucidate the mechanism of pH-induced refolding of diphtheria toxin T-domain on membranes in order to understand how the protein translocates its catalytic domain across endosomal membranes. (4) Determine if so-called """"""""Trojan"""""""" peptides - such as penetratin and TAT - can cross pure lipid bilayers unaided, and if so, under what conditions. (5) Expand and improve physicochemical rules for predicting the binding and folding of peptides at membrane interfaces, and establish a structural context for them.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM046823-11
Application #
6636042
Study Section
Biophysical Chemistry Study Section (BBCB)
Program Officer
Chin, Jean
Project Start
1992-09-30
Project End
2005-03-31
Budget Start
2003-04-01
Budget End
2004-03-31
Support Year
11
Fiscal Year
2003
Total Cost
$234,240
Indirect Cost
Name
University of California Irvine
Department
Physiology
Type
Schools of Medicine
DUNS #
046705849
City
Irvine
State
CA
Country
United States
Zip Code
92697
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Jaud, Simon; Fernández-Vidal, Mónica; Nilsson, Ingmarie et al. (2009) Insertion of short transmembrane helices by the Sec61 translocon. Proc Natl Acad Sci U S A 106:11588-93
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Fernandez-Vidal, Monica; Jayasinghe, Sajith; Ladokhin, Alexey S et al. (2007) Folding amphipathic helices into membranes: amphiphilicity trumps hydrophobicity. J Mol Biol 370:459-70
Benz, Ryan W; Nanda, Hirsh; Castro-Roman, Francisco et al. (2006) Diffraction-based density restraints for membrane and membrane-peptide molecular dynamics simulations. Biophys J 91:3617-29
Castro-Roman, Francisco; Benz, Ryan W; White, Stephen H et al. (2006) Investigation of finite system-size effects in molecular dynamics simulations of lipid bilayers. J Phys Chem B 110:24157-64
Hristova, Kalina; White, Stephen H (2005) An experiment-based algorithm for predicting the partitioning of unfolded peptides into phosphatidylcholine bilayer interfaces. Biochemistry 44:12614-9
Hessa, Tara; White, Stephen H; von Heijne, Gunnar (2005) Membrane insertion of a potassium-channel voltage sensor. Science 307:1427
Benz, Ryan W; Castro-Roman, Francisco; Tobias, Douglas J et al. (2005) Experimental validation of molecular dynamics simulations of lipid bilayers: a new approach. Biophys J 88:805-17

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