Secondary structure analysis of tubulin and microtubules with Raman spectroscopy

Biochim Biophys Acta. 1989 Jun 13;996(1-2):110-5. doi: 10.1016/0167-4838(89)90102-7.

Abstract

Raman spectroscopy is used to study the secondary structure of tubulin in the assembled and the dissociated states from the analysis of the amide-I band. Essentially two states are recognized: the GTP- and the GDP-bound state, differing in alpha-helix and antiparallel beta-sheet content. Microtubules give a spectrum which is very similar to the GDP-bound state. MAPs and temperature have minor effects, while increasing the pH up to 8 causes a reduction in alpha-helix content and a increase in antiparallel beta-sheet. The binding of demecolcine also induces structural changes which are similar to the GDP-bound state.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amides
  • Animals
  • Demecolcine / pharmacology
  • Guanosine Diphosphate / metabolism
  • Hydrogen-Ion Concentration
  • Macromolecular Substances
  • Microtubule-Associated Proteins / pharmacology
  • Microtubules / ultrastructure*
  • Polymers
  • Protein Binding
  • Spectrum Analysis, Raman
  • Swine
  • Temperature
  • Tubulin / ultrastructure*

Substances

  • Amides
  • Macromolecular Substances
  • Microtubule-Associated Proteins
  • Polymers
  • Tubulin
  • Guanosine Diphosphate
  • Demecolcine