Genetically dominant mutations in the gene that encodes peripheral myelin protein 22 (PMP22) lead to single amino acid changes in its sequence that result in defective myelin, underlying the common human peripheral neuropathy, Charcot-Marie-Tooth Disease Type IA (CMTD). It is believed that CMTD mutations result in misassembly of PMP22 early in the secretory pathway, resulting in the loss of protein function and also in the formation of potentially cytotoxic aggregates. The overall goal of this project is to elucidate the molecular biophysical nature of the perturbations made by CMTD-associated mutations to the structure, stability and folding of this critical membrane protein. We also seek to test whether chemical chaperones can correct the folding defects normally observed for CMTD mutant forms of PMP22.
Aim 1. Characterize the structures of the wild type (WT) and CMTD mutant forms of human PMP22 using NMR spectroscopy.
Aim 1 will test the hypothesis that CMTD mutant forms of PMP22 differ from the WT protein in terms of conformation and/or oligomeric state. Structural information will also illuminate PMP22's structure/function relationships and its role in myelin production and maintenance, and will provide biophysical insight into how amino acid mutations result in CMTD. Determination of PMP22's structure will also add to the currently sparse gallery of human membrane protein structures.
Aim 2. Characterize the stability and folding kinetics of WT and CMTD mutant forms of PMP22.
Aim 2 will test the hypothesis that disease-related mutations of PMP22 destabilize the protein.
Aim 2 will also test the hypothesis that disease-related mutant forms of PMP22 fold more slowly and/or inefficiently than the wild type protein. We will also test whether CMTD mutant forms of PMP22 are aggregation-prone.
Aim 3. Determine whether chemical chaperones can increase the cell surface expression of CMTD mutant forms of PMP22.
Aim 3 will test the hypothesis that PMP22 is akin to other human membrane proteins that are linked to diseases involving protein misassembly and for which it has already been established that proper folding and trafficking can be restored using chemical chaperones.

Public Health Relevance

Studies of the structure, folding, and stability of the human peripheral myelin protein 22 (PMP22) will be undertaken to unravel the molecular basis for Charcot-Marie Tooth Disease, a peripheral neuropathy. Results from this work are expected to contribute to novel therapeutic strategies for this human disease.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
1R01NS058815-01A2
Application #
7882031
Study Section
Macromolecular Structure and Function C Study Section (MSFC)
Program Officer
Gwinn, Katrina
Project Start
2010-04-01
Project End
2013-03-31
Budget Start
2010-04-01
Budget End
2011-03-31
Support Year
1
Fiscal Year
2010
Total Cost
$310,000
Indirect Cost
Name
Vanderbilt University Medical Center
Department
Biochemistry
Type
Schools of Medicine
DUNS #
004413456
City
Nashville
State
TN
Country
United States
Zip Code
37212
Mittendorf, Kathleen F; Marinko, Justin T; Hampton, Cheri M et al. (2017) Peripheral myelin protein 22 alters membrane architecture. Sci Adv 3:e1700220
Schlebach, Jonathan P; Narayan, Malathi; Alford, Catherine et al. (2015) Conformational Stability and Pathogenic Misfolding of the Integral Membrane Protein PMP22. J Am Chem Soc 137:8758-68
Song, Yuanli; Mittendorf, Kathleen F; Lu, Zhenwei et al. (2014) Impact of bilayer lipid composition on the structure and topology of the transmembrane amyloid precursor C99 protein. J Am Chem Soc 136:4093-6
Song, Yuanli; Kenworthy, Anne K; Sanders, Charles R (2014) Cholesterol as a co-solvent and a ligand for membrane proteins. Protein Sci 23:1-22
Wu, Jiawen; Peng, Dungeng; Voehler, Markus et al. (2013) Structure and expression of a novel compact myelin protein - small VCP-interacting protein (SVIP). Biochem Biophys Res Commun 440:173-8
Schlebach, Jonathan P; Peng, Dungeng; Kroncke, Brett M et al. (2013) Reversible folding of human peripheral myelin protein 22, a tetraspan membrane protein. Biochemistry 52:3229-41
Barrett, Paul J; Chen, Jiang; Cho, Min-Kyu et al. (2013) The quiet renaissance of protein nuclear magnetic resonance. Biochemistry 52:1303-20
Mittendorf, Kathleen F; Deatherage, Catherine L; Ohi, Melanie D et al. (2012) Tailoring of membrane proteins by alternative splicing of pre-mRNA. Biochemistry 51:5541-56
Van Horn, Wade D; Sanders, Charles R (2012) Prokaryotic diacylglycerol kinase and undecaprenol kinase. Annu Rev Biophys 41:81-101
Sakakura, Masayoshi; Hadziselimovic, Arina; Wang, Zhen et al. (2011) Structural basis for the Trembler-J phenotype of Charcot-Marie-Tooth disease. Structure 19:1160-9

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