Pseudocatalytic Antiaggregation Activity of Antibodies: Immunoglobulins can Influence α-Synuclein Aggregation at Substoichiometric Concentrations

Mol Neurobiol. 2016 Apr;53(3):1949-1958. doi: 10.1007/s12035-015-9148-8. Epub 2015 Apr 2.

Abstract

Protein aggregation is involved in a variety of diseases. Alteration of the aggregation pathway, either to produce less toxic structures or to increase aggregate clearance, is a promising therapeutic route. Both active and passive immunization has been used for this purpose. However, the mechanism of action of antibodies on protein aggregates is not completely clear especially given poor ability of antibodies to cross blood-brain barrier. Here, we have shown that antibodies can interfere with protein aggregation at substoichiometric concentrations (as low as 1:1000 antibody to protein ratio). This is an indication that antibodies interact with aggregation intermediates in chaperone-like manner altering the aggregation pathways at very low antibody levels. This observation supports earlier suggestions that antibodies can inhibit aggregation by interaction with low abundance aggregation intermediates.

Keywords: Antibodies; Parkinson’s disease; Protein aggregation; α-Synuclein.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies / metabolism*
  • Antibodies / pharmacology
  • Benzothiazoles
  • Biocatalysis
  • Biological Assay
  • Circular Dichroism
  • Fluorescence
  • Kinetics
  • Protein Aggregates* / drug effects
  • Protein Aggregation, Pathological
  • Thiazoles / metabolism
  • alpha-Synuclein / chemistry*
  • alpha-Synuclein / metabolism*
  • alpha-Synuclein / ultrastructure

Substances

  • Antibodies
  • Benzothiazoles
  • Protein Aggregates
  • Thiazoles
  • alpha-Synuclein
  • thioflavin T