A solution NMR investigation into the impaired self-assembly properties of two murine amelogenins containing the point mutations T21→I or P41→T
Journal Article
·
· Archives of Biochemistry and Biophysics, 537(2):217-224
Amelogenesis imperfecta describes a group of inherited disorders that results in defective tooth enamel. Two disorders associated with human amelogenesis imperfecta are the point mutations T21?I or P40?T in amelogenin, the dominant protein present during the early stages of enamel biomineralization. The biophysical properties of wildtype murine amelogenin (M180) and two proteins containing the equivalent mutations in murine amelogenin, T21?I (M180-I) and P41?T (M180-T), were probed by NMR spectroscopy. At low protein concentration (0.1 mM), M180, M180-I, and M180-T are predomi- nately monomeric at pH 3.0 in 2% acetic acid and neither mutation produces a major structural change. Chemical shift perturbation studies as a function of protein (0.1–1.8 mM) or NaCl (0–400 mM) concentra- tions show that the mutations affect the self-association properties by causing self-assembly at lower protein or salt concentrations, relative to wildtype amelogenin, with the largest effect observed for M180-I. Under both conditions, the premature self-assembly is initiated near the N-terminus, providing further evidence for the importance of this region in the self-assembly process. The self-association of M180-I and M180-T at lower protein concentrations and lower ionic strengths than wildtype M180 may account for the clinical phenotypes of these mutations, defective enamel formation.
- Research Organization:
- Pacific Northwest National Laboratory (PNNL), Richland, WA (US), Environmental Molecular Sciences Laboratory (EMSL)
- Sponsoring Organization:
- USDOE
- DOE Contract Number:
- AC05-76RL01830
- OSTI ID:
- 1091431
- Report Number(s):
- PNNL-SA-94926; 44691; 47735; 41891; 40112; 400412000
- Journal Information:
- Archives of Biochemistry and Biophysics, 537(2):217-224, Journal Name: Archives of Biochemistry and Biophysics, 537(2):217-224
- Country of Publication:
- United States
- Language:
- English
Similar Records
Improved protocol to purify untagged amelogenin – Application to murine amelogenin containing the equivalent P70→T point mutation observed in human amelogenesis imperfecta
Amelogenin signal peptide mutation: Correlation between mutations in the amelogenin gene (AMGX) and manifestations of X-linked amelogenesis imperfecta
The energetic basis for hydroxyapatite mineralization by amelogenin variants provides insights into the origin ofamelogenesis imperfecta
Journal Article
·
Sun Oct 12 20:00:00 EDT 2014
· Protein Expression and Purification
·
OSTI ID:1167286
Amelogenin signal peptide mutation: Correlation between mutations in the amelogenin gene (AMGX) and manifestations of X-linked amelogenesis imperfecta
Journal Article
·
Tue Feb 28 23:00:00 EST 1995
· Genomics
·
OSTI ID:249977
The energetic basis for hydroxyapatite mineralization by amelogenin variants provides insights into the origin ofamelogenesis imperfecta
Journal Article
·
Mon Jun 24 20:00:00 EDT 2019
· Proceedings of the National Academy of Sciences of the United States of America
·
OSTI ID:1776573