Enveloped viruses enter cells using fusion proteins to merge the virus envelope and the cell membrane. Determining the atomic-level structures and structural changes of viral fusion proteins along the fusion pathway is important both for fundamental understanding of how proteins mediate membrane-curvature generation and for potentially developing antiviral drugs to inhibit virus entry. High-resolution structural information of the membrane-bound fusion peptide (FP) and transmembrane (TM) domains in viral fusion proteins is so far limited. We propose to investigate the FP and TM domains of the HIV and parainfluenza virus 5 (PIV5) fusion proteins, using high-resolution solid-state NMR spectroscopy.
Aim 1 will examine the oligomeric structure of the PIV5 FP and TM peptides in lipid membranes of different compositions to understand early-fusion structures.
In Aim 2, we will investigate the structure of a fusion protein chimera that links the FP and TM segments, in order to understand late-fusion structures. By measuring inter-domain FP-TM contacts and homo-oligomeric association, we will determine whether the FP and TM form a six-helix bundle in the lipid membrane, similar to the ectodomain six-helix bundle outside the membrane.
In Aim 3, we will investigate the MPER- TM structure of the HIV fusion protein, gp41. We will conduct 19F-19F and 13C-19F distance experiments to measure the three-dimensional fold and oligomeric structure of this antibody- targeted region of the protein. These experiments should provide fundamental insights into the protein structural transitions that underlie virus-cell fusion.

Public Health Relevance

Enveloped viruses use their fusion proteins to merge the virus lipid envelope and the cell membrane to enter cells. Knowledge of the three-dimensional structures of these fusion proteins in lipid membranes is important for designing vaccines and antiviral drugs to inhibit viral entry. We will use solid-state NMR spectroscopy to determine the structures of two crucial membrane-bound domains in the fusion proteins of two viruses: the human immunodeficiency virus, which infects ~37 million people worldwide, and the parainfluenza virus responsible for many infant respiratory diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
3R01GM066976-14A1S1
Application #
9702953
Study Section
Program Officer
Preusch, Peter
Project Start
2003-02-01
Project End
2022-01-31
Budget Start
2018-02-01
Budget End
2019-01-31
Support Year
14
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Massachusetts Institute of Technology
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
001425594
City
Cambridge
State
MA
Country
United States
Zip Code
Kwon, Byungsu; Lee, Myungwoon; Waring, Alan J et al. (2018) Oligomeric Structure and Three-Dimensional Fold of the HIV gp41 Membrane-Proximal External Region and Transmembrane Domain in Phospholipid Bilayers. J Am Chem Soc 140:8246-8259
Roos, Matthias; Wang, Tuo; Shcherbakov, Alexander A et al. (2018) Fast Magic-Angle-Spinning 19F Spin Exchange NMR for Determining Nanometer 19F-19F Distances in Proteins and Pharmaceutical Compounds. J Phys Chem B 122:2900-2911
Gelenter, Martin D; Hong, Mei (2018) Efficient 15N-13C Polarization Transfer by Third-Spin-Assisted Pulsed Cross-Polarization Magic-Angle-Spinning NMR for Protein Structure Determination. J Phys Chem B 122:8367-8379
Lee, Myungwoon; Yao, Hongwei; Kwon, Byungsu et al. (2018) Conformation and Trimer Association of the Transmembrane Domain of the Parainfluenza Virus Fusion Protein in Lipid Bilayers from Solid-State NMR: Insights into the Sequence Determinants of Trimer Structure and Fusion Activity. J Mol Biol 430:695-709
Shcherbakov, Alexander A; Hong, Mei (2018) Rapid measurement of long-range distances in proteins by multidimensional 13C-19F REDOR NMR under fast magic-angle spinning. J Biomol NMR 71:31-43
Mandala, Venkata S; Williams, Jonathan K; Hong, Mei (2018) Structure and Dynamics of Membrane Proteins from Solid-State NMR. Annu Rev Biophys 47:201-222
Liao, Shu Y; Lee, Myungwoon; Hong, Mei (2018) Interplay between membrane curvature and protein conformational equilibrium investigated by solid-state NMR. J Struct Biol :
Wang, Tuo; Jo, Hyunil; DeGrado, William F et al. (2017) Water Distribution, Dynamics, and Interactions with Alzheimer's ?-Amyloid Fibrils Investigated by Solid-State NMR. J Am Chem Soc 139:6242-6252
Lee, Myungwoon; Wang, Tuo; Makhlynets, Olga V et al. (2017) Zinc-binding structure of a catalytic amyloid from solid-state NMR. Proc Natl Acad Sci U S A 114:6191-6196
Fritzsching, Keith J; Hong, Mei; Schmidt-Rohr, Klaus (2016) Conformationally selective multidimensional chemical shift ranges in proteins from a PACSY database purged using intrinsic quality criteria. J Biomol NMR 64:115-30

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