Rapid binding of synapsin I to F- and G-actin. A study using fluorescence resonance energy transfer

FEBS Lett. 1993 Aug 30;329(3):301-5. doi: 10.1016/0014-5793(93)80242-m.

Abstract

Synapsin I is a nerve terminal phosphoprotein which interacts with synaptic vesicles and actin in a phosphorylation-dependent manner. By using fluorescence resonance energy transfer between purified components labeled with fluorescent probes, we now show that the binding of synapsin I to actin is a rapid phenomenon. Binding of synapsin I to actin can also be demonstrated when synaptic vesicles are present in the medium and appears to be modulated by ionic strength and synapsin I phosphorylation.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Actins / metabolism*
  • Animals
  • Binding Sites
  • Cattle
  • Spectrometry, Fluorescence
  • Synapsins / metabolism*

Substances

  • Actins
  • Synapsins