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Micro-heterogeneity and aggregation in beta2-microglobulin solutions: effects of temperature, pH, and conformational variant addition.
- Source :
-
European biophysics journal : EBJ [Eur Biophys J] 2006 May; Vol. 35 (5), pp. 439-45. Date of Electronic Publication: 2006 Mar 07. - Publication Year :
- 2006
-
Abstract
- We show that beta(2)-microglobulin solutions in physiological conditions contain a tiny fraction of aggregates, which can hardly be filtered out and tend to re-form spontaneously. At physiological pH the fractional amount and size distribution of the latter aggregates do not depend on temperature. Conversely, in the pH range typical of the peri-articular tissue acidosis that often occurs in hemodialysis, temperature increase leads to fast and irreversible growth of the aggregates. Quite similar, but strongly enhanced aggregation effects can be induced even in physiological conditions by adding a very small amount of DeltaN6, a naturally occurring truncated isoform of beta(2)-m known to promote fibrillogenesis.
- Subjects :
- Computer Simulation
Hydrogen-Ion Concentration
Microchemistry methods
Multiprotein Complexes chemistry
Multiprotein Complexes ultrastructure
Particle Size
Protein Conformation
Solutions
Temperature
Models, Chemical
Models, Molecular
beta 2-Microglobulin chemistry
beta 2-Microglobulin ultrastructure
Subjects
Details
- Language :
- English
- ISSN :
- 0175-7571
- Volume :
- 35
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- European biophysics journal : EBJ
- Publication Type :
- Academic Journal
- Accession number :
- 16520957
- Full Text :
- https://doi.org/10.1007/s00249-006-0051-0