The structure-function paradigm is a powerful guiding principle that underlies much of our understanding of biological processes. What is often neglected in this picture, however, is the flexibility of protein structures. This flexibility is necessary for a protein to fold to its native, active structure. Furthermore, protein function requires evolution of this native structure with time. Therefore, the dynamics of the protein structure and associated solvent water provide the critical connection between structure and function. The overall goal of this proposal is to elucidate the functional dynamics of hemagglutinin and M2 proton channel that enable influenza virus infection, a problem with significant public health implications. The mechanisms explored in this work are also relevant to other enveloped viruses, in particular HIV. More generally, membrane fusion and proton transport through proteins are of high fundamental interest and we expect the insight gained in these specific studies will contribute to the understanding of a broad range of related systems. We plan to pursue three specific aims: 1) Determine the mechanism of hemagglutinin mediated membrane fusion. We will test a new model for protein mediated membrane fusion that is based on molecular dynamics simulations of this process. We have developed unique methodology base on a laser induced pH jump to initiate the fusion process, and structure specific spectroscopic methods to characterize the hemagglutinin refolding dynamics that drive membrane fusion. This viral protein serves as an archetype for understanding the general mechanism of membrane fusion as a ubiquitous membrane transport process. 2) Determine the mechanism of fusion pore formation. We will test the hypothesis that the hemagglutinin trans-membrane domain (TMD) and fusion peptide (FP) form an oligomeric complex that opens and stabilizes the fusion pore. 3) Determine the molecular mechanism of actively gated proton transport. This work will on a focus on the influenza M2 proton channel, an important model ion channel. Understanding transport of protons through protein channels is critical to many essential biological processes as well as replication of the influenza virus.
These aims are linked intellectually by energy landscape concepts and operationally by the methodology developed in our lab for studying both protein and membrane dynamics. Our unique approach will allow us to identify specific protein motions involved in protein mediated membrane fusion and proton channel activation. We expect this work to provide important new insight into the factors that shape the energy landscape of membrane proteins and the coupled membrane dynamics.
(relevance to public health) Proteins are dynamic molecular machines that carry out essential cellular functions as well as pathological processes related to disease states, including infection by enveloped viruses such as influenza and HIV. A better understanding of the mechanisms of these dynamic protein structures is of critical importance to immunological strategies aimed at preventing and treating these diseases. The results from the proposed research will elucidate protein structural dynamics involved in viral infection, including membrane fusion mediated by the influenza protein hemagglutinin and viral replication triggered by the pH activated M2 proton channel.
| Dyer, R Brian; Eller, Micah W (2018) Dynamics of hemagglutinin-mediated membrane fusion. Proc Natl Acad Sci U S A 115:8655-8657 |
| Nagarajan, Sureshbabu; Xiao, Shifeng; Raleigh, Daniel P et al. (2018) Heterogeneity in the Folding of Villin Headpiece Subdomain HP36. J Phys Chem B : |
| Zhao, Jing; Su, Hanquan; Vansuch, Gregory E et al. (2018) Localized Nanoscale Heating Leads to Ultrafast Hydrogel Volume-Phase Transition. ACS Nano : |
| Siaw, Hew Ming Helen; Raghunath, Gokul; Dyer, R Brian (2018) Peripheral Protein Unfolding Drives Membrane Bending. Langmuir 34:8400-8407 |
| Su, Hanquan; Liu, Zheng; Liu, Yang et al. (2018) Light-Responsive Polymer Particles as Force Clamps for the Mechanical Unfolding of Target Molecules. Nano Lett 18:2630-2636 |
| Reid, Keon A; Davis, Caitlin M; Dyer, R Brian et al. (2018) Binding, folding and insertion of a ?-hairpin peptide at a lipid bilayer surface: Influence of electrostatics and lipid tail packing. Biochim Biophys Acta Biomembr 1860:792-800 |
| Davis, Caitlin M; Reddish, Michael J; Dyer, R Brian (2017) Dual time-resolved temperature-jump fluorescence and infrared spectroscopy for the study of fast protein dynamics. Spectrochim Acta A Mol Biomol Spectrosc 178:185-191 |
| Zanetti-Polzi, Laura; Davis, Caitlin M; Gruebele, Martin et al. (2017) Parallel folding pathways of Fip35 WW domain explained by infrared spectra and their computer simulation. FEBS Lett 591:3265-3275 |
| Jeong, Ban-Seok; Dyer, R Brian (2017) Proton Transport Mechanism of M2 Proton Channel Studied by Laser-Induced pH Jump. J Am Chem Soc 139:6621-6628 |
| Schuler, Erin E; Nagarajan, Sureshbabu; Dyer, R Brian (2016) Submillisecond Dynamics of Mastoparan X Insertion into Lipid Membranes. J Phys Chem Lett 7:3365-70 |
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