Membrane proteins play an essential role in controlling the movement of material and information in and out of the cell, in determining the flow and use of energy, as well as in triggering the initiation of numerous signaling pathways. To fulfill these roles, conformational and interaction dynamics exert a dominant influence on their functional behavior, for it is the interplay between structure and dynamics what ultimately defines their function. The Membrane Protein Structural Dynamics Consortium (MPSDC) is proposed as a highly interactive, tightly integrated and multidisciplinary effort focused on elucidating the relationship between structure, dynamics and function in a variety of membrane proteins. The MMPSD will be organized around multidisciplinary project teams formed by investigators from 14 institutions in five different countries. These teams will study major mechanistic questions associated with membrane protein function as it relates to two major areas: energy transduction in signaling (ion channels and receptors) and energy inter-conversion (transporters and pumps). Ultimately, our goal is to decode the general mechanistic principles that govern protein movement and its associated fluctuation dynamics by dissecting and analyzing the molecular and dynamical bases of these functions at an unprecedented and quantitative level, as well as exploiting this information to engineer altered and novel activities into membrane protein frameworks to rationally evolve new functions. To accomplish its goals, the MPSDC will develop in parallel a set of tools, concepts and reagents to: 1) Apply state of the art spectroscopic methods (Magnetic Resonance, Fluorescence, 2D-IR) to follow conformational changes and dynamics of the determined structures;2) Correlate dynamic measurements with high-resolution ensemble and single molecule functional measurements;and 3) Design and implement novel computational approaches to link static and dynamic data with function. Six core facilities will feed and interconnect with the individual projects in a highly interactive way. The cores will act as both, """"""""innovation incubators"""""""" and research support centers by providing service and expertise In these critical areas: Membrane protein expression, the establishment of chemical synthesis capabilities for probes and detergents, the generation of a variety of binders and other crystallization chaperones and other target binders, the development of common computational tools to interpret and integrate the wealth of experimental data, the generation of novel, highly specific synthetic toxins and the continuous discovery of novel targets through the use of metagenomics tools.

Public Health Relevance

The interplay between structure and dynamics what ultimately defines a biological system's functional mechanism. Knowledge of how these fundamental phenomena influence the way membrane proteins function will be required to understand both the complex web of signaling and energy transduction mechanisms required for normal cellular function and their pathologies.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Specialized Center--Cooperative Agreements (U54)
Project #
1U54GM087519-01A1
Application #
7900160
Study Section
Special Emphasis Panel (ZGM1-CBB-3 (GL))
Program Officer
Chin, Jean
Project Start
2010-08-10
Project End
2015-06-30
Budget Start
2010-08-10
Budget End
2011-06-30
Support Year
1
Fiscal Year
2010
Total Cost
$4,793,068
Indirect Cost
Name
University of Chicago
Department
Biochemistry
Type
Schools of Medicine
DUNS #
005421136
City
Chicago
State
IL
Country
United States
Zip Code
60637
Infield, Daniel T; Matulef, Kimberly; Galpin, Jason D et al. (2018) Main-chain mutagenesis reveals intrahelical coupling in an ion channel voltage-sensor. Nat Commun 9:5055
Martens, Chloe; Shekhar, Mrinal; Borysik, Antoni J et al. (2018) Direct protein-lipid interactions shape the conformational landscape of secondary transporters. Nat Commun 9:4151
Vermaas, Josh V; Rempe, Susan B; Tajkhorshid, Emad (2018) Electrostatic lock in the transport cycle of the multidrug resistance transporter EmrE. Proc Natl Acad Sci U S A 115:E7502-E7511
Bailey, Lucas J; Sheehy, Kimberly M; Dominik, Pawel K et al. (2018) Locking the Elbow: Improved Antibody Fab Fragments as Chaperones for Structure Determination. J Mol Biol 430:337-347
Huang, Shengdian; Zhang, Hui; Paletta, Joseph T et al. (2018) Reduction kinetics and electrochemistry of tetracarboxylate nitroxides. Free Radic Res 52:327-334
Abramyan, Ara M; Quick, Matthias; Xue, Catherine et al. (2018) Exploring Substrate Binding in the Extracellular Vestibule of MhsT by Atomistic Simulations and Markov Models. J Chem Inf Model 58:1244-1252
Mahinthichaichan, Paween; Gennis, Robert B; Tajkhorshid, Emad (2018) Bacterial denitrifying nitric oxide reductases and aerobic respiratory terminal oxidases use similar delivery pathways for their molecular substrates. Biochim Biophys Acta Bioenerg 1859:712-724
Nanazashvili, Mikheil; Sánchez-Rodríguez, Jorge E; Fosque, Ben et al. (2018) LRET Determination of Molecular Distances during pH Gating of the Mammalian Inward Rectifier Kir1.1b. Biophys J 114:88-97
Min, Duyoung; Jefferson, Robert E; Qi, Yifei et al. (2018) Unfolding of a ClC chloride transporter retains memory of its evolutionary history. Nat Chem Biol 14:489-496
Infield, Daniel T; Lueck, John D; Galpin, Jason D et al. (2018) Orthogonality of Pyrrolysine tRNA in the Xenopus oocyte. Sci Rep 8:5166

Showing the most recent 10 out of 282 publications