Literature DB >> 9774536

Temperature and pH-dependent supramolecular self-assembly of amelogenin molecules: a dynamic light-scattering analysis.

J Moradian-Oldak1, W Leung, A G Fincham.   

Abstract

Evidence for the molecular self-assembly of amelogenin proteins to form quasi-spherical particles ("nanospheres") in solution, both in vitro and in vivo, has recently been documented. A particle-size distribution analysis of dynamic light-scattering data was undertaken to investigate the influence of temperature on this molecular self-assembly process at three different pH's. The long-term objective was to correlate these observations to the unusual physiochemical characteristics of the protein, to improve understanding of the molecular mechanisms involved in the generation of amelogenin "nanospheres" and understanding of their putative relation to amelogenin function in vivo. We analyzed data using two different algorithms: Dynamics and DynaLS. It was found that at pH 8, in a temperature range between 5 and 25 degrees C, the size of the recombinant amelogenin nanospheres is monodisperse, giving rise to particles of 15-18 nm in hydrodynamic radius. However, heterogeneous distribution of particle size was observed at temperature ranges between 27 and 35 degrees C, becoming monodisperse again with larger particles (60-70 nm) after the temperature was elevated to 37-40 degrees C. We interpret these results to suggest that amelogenin molecular self-association possesses a second stage assembly process at temperatures of 30-35 degrees C, creating larger entities which apparently are structured and stable at 37-40 degreesC. The effect of pH on the size of amelogenin "aggregates" was much more noticeable at 37 degrees C compared to that at 25 degrees C. This observation suggests that at physiological temperature (i.e., 37 degrees C) amelogenin molecular self-assembly is extremely sensitive to pH changes. This finding supports the notion that local pH changes in the microenvironment of the enamel extracellular matrix may play critical roles in controlling the structural organization of the organic matrix framework. Copyright 1998 Academic Press.

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Year:  1998        PMID: 9774536     DOI: 10.1006/jsbi.1998.4008

Source DB:  PubMed          Journal:  J Struct Biol        ISSN: 1047-8477            Impact factor:   2.867


  36 in total

1.  Amelogenin Promotes the Formation of Elongated Apatite Microstructures in a Controlled Crystallization System.

Authors:  Lijun Wang; Xiangying Guan; Chang Du; Janet Moradian-Oldak; George H Nancollas
Journal:  J Phys Chem C Nanomater Interfaces       Date:  2007-05-03       Impact factor: 4.126

2.  Effects of phosphorylation on the self-assembly of native full-length porcine amelogenin and its regulation of calcium phosphate formation in vitro.

Authors:  Felicitas B Wiedemann-Bidlack; Seo-Young Kwak; Elia Beniash; Yasuo Yamakoshi; James P Simmer; Henry C Margolis
Journal:  J Struct Biol       Date:  2010-11-11       Impact factor: 2.867

3.  Enamel inspired nanocomposite fabrication through amelogenin supramolecular assembly.

Authors:  Yuwei Fan; Zhi Sun; Rizhi Wang; Christopher Abbott; Janet Moradian-Oldak
Journal:  Biomaterials       Date:  2007-02-22       Impact factor: 12.479

4.  Purification, crystallization and preliminary X-ray analysis of Enterococcus faecium aminoglycoside-2''-phosphotransferase-Ib [APH(2'')-Ib].

Authors:  Rupa Walanj; Paul Young; Heather M Baker; Edward N Baker; Peter Metcalf; Joseph W Chow; Stephen Lerner; Sergei Vakulenko; Clyde A Smith
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2005-04-01

5.  pH triggered self-assembly of native and recombinant amelogenins under physiological pH and temperature in vitro.

Authors:  Felicitas B Wiedemann-Bidlack; Elia Beniash; Yasuo Yamakoshi; James P Simmer; Henry C Margolis
Journal:  J Struct Biol       Date:  2007-07-04       Impact factor: 2.867

6.  Mimicking the Self-Organized Microstructure of Tooth Enamel.

Authors:  Lijun Wang; Xiangying Guan; Haoyong Yin; Janet Moradian-Oldak; George H Nancollas
Journal:  J Phys Chem C Nanomater Interfaces       Date:  2008-03-22       Impact factor: 4.126

7.  Intrinsically disordered proteins drive enamel formation via an evolutionarily conserved self-assembly motif.

Authors:  Tomas Wald; Frantisek Spoutil; Adriana Osickova; Michaela Prochazkova; Oldrich Benada; Petr Kasparek; Ladislav Bumba; Ophir D Klein; Radislav Sedlacek; Peter Sebo; Jan Prochazka; Radim Osicka
Journal:  Proc Natl Acad Sci U S A       Date:  2017-02-14       Impact factor: 11.205

8.  Zeta-potential and particle size analysis of human amelogenins.

Authors:  V Uskokovic; Z Castiglione; P Cubas; L Zhu; W Li; S Habelitz
Journal:  J Dent Res       Date:  2009-12-29       Impact factor: 6.116

9.  Sequence-Defined Energetic Shifts Control the Disassembly Kinetics and Microstructure of Amelogenin Adsorbed onto Hydroxyapatite (100).

Authors:  Jinhui Tao; Garry W Buchko; Wendy J Shaw; James J De Yoreo; Barbara J Tarasevich
Journal:  Langmuir       Date:  2015-09-18       Impact factor: 3.882

10.  Polyelectrolyte-mediated adsorption of amelogenin monomers and nanospheres forming mono- or multilayers.

Authors:  Csilla Gergely; Balazs Szalontai; Janet Moradian-Oldak; Frédéric J G Cuisinier
Journal:  Biomacromolecules       Date:  2007-06-19       Impact factor: 6.988

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