Identification of syntaxin 1A as a novel binding protein for presenilin-1

Brain Res Mol Brain Res. 2000 May 31;78(1-2):100-7. doi: 10.1016/s0169-328x(00)00079-6.

Abstract

Mutations in the presenilin 1 gene have been shown to result in Alzheimer's disease. Presenilin 1 is a multi-transmembrane protein with a large hydrophilic loop near the C-terminus. This region is required for known functions of presenilin 1. We have constrained this loop within the active site of the bacterial protein, thioredoxin, to mimic its native conformational state. This hybrid protein was used as bait in a yeast two hybrid screen in an attempt to identify presenilin binding proteins. By this method syntaxin 1A, a synaptic plasma membrane protein, was identified as a novel binding protein for presenilin 1. In vitro experiments confirm the two-hybrid results suggesting that PS1 binds syntaxin under physiological conditions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alzheimer Disease / metabolism
  • Antigens, Surface / chemistry*
  • Antigens, Surface / genetics
  • Antigens, Surface / metabolism*
  • Cell Membrane / metabolism
  • Cloning, Molecular
  • Gene Expression / physiology
  • Glycerol
  • Humans
  • Membrane Proteins / chemistry*
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Molecular Weight
  • Nerve Tissue Proteins / chemistry*
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism*
  • Neurons / metabolism
  • Precipitin Tests
  • Presenilin-1
  • Protein Binding / physiology
  • Protein Structure, Tertiary
  • Subcellular Fractions / chemistry
  • Synaptic Vesicles / metabolism
  • Syntaxin 1
  • Thioredoxins / chemistry
  • Thioredoxins / genetics
  • Two-Hybrid System Techniques

Substances

  • Antigens, Surface
  • Membrane Proteins
  • Nerve Tissue Proteins
  • PSEN1 protein, human
  • Presenilin-1
  • STX1A protein, human
  • Syntaxin 1
  • Thioredoxins
  • Glycerol