Fluorescence approaches to the study of the actin-nucleating and bundling activities of synapsin I

J Physiol Paris. 1993;87(2):117-22. doi: 10.1016/0928-4257(93)90005-e.

Abstract

Synapsin I is a neuron-specific phosphoprotein which binds to small synaptic vesicles and actin in a phosphorylation-dependent fashion. We have analyzed the ability of synapsin I to interact with actin monomers and filaments using purified proteins derivatized with fluorescent probes. Synapsin I accelerates the initial rate of actin polymerization and increases the final steady-state levels of polymerized actin. The fraction of total actin polymerized by synapsin I strongly depends on the synapsin I-actin ratio. We have visualized the actin-bundling activity of synapsin I using a non-perturbing method, video-enhanced microscopy of fluoresceinated synapsin I and actin filaments. Our findings suggest that synapsin I exerts a control on the physical characteristics of the cytoskeletal network of the nerve terminal and are consistent with the proposed role of synapsin I in mediating the interaction of synaptic vesicles with actin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / physiology*
  • Animals
  • Cattle
  • Fluorescein
  • Fluoresceins
  • Fluorometry
  • Microscopy / methods
  • Polymers / metabolism
  • Synapsins / physiology*
  • Television

Substances

  • Actins
  • Fluoresceins
  • Polymers
  • Synapsins
  • Fluorescein

Grants and funding