Capturing protein interactions in the secretory pathway of living cells

Proc Natl Acad Sci U S A. 2005 May 3;102(18):6350-5. doi: 10.1073/pnas.0501976102. Epub 2005 Apr 22.

Abstract

The secretory pathway is composed of membrane compartments specialized in protein folding, modification, transport, and sorting. Numerous transient protein-protein interactions guide the transport-competent proteins through the secretory pathway. Here we have adapted the yellow fluorescent protein (YFP)-based protein fragment complementation assay (PCA) to detect protein-protein interactions in the secretory pathway of living cells. Fragments of YFP were fused to the homooligomeric cargo-receptor lectin endoplasmic reticulum Golgi intermediate compartment (ERGIC)-53, to the ERGIC-53-interacting multi-coagulation factor deficiency protein MCFD2, and to ERGIC-53's cargo glycoprotein cathepsin Z. YFP PCA analysis revealed the oligomerization of ERGIC-53 and its interaction with MCFD2, as well as its lectin-mediated interaction with cathepsin Z. Mutation of the lectin domain of ERGIC-53 selectively decreased YFP complementation with cathepsin Z. Using YFP PCA, we discovered a carbohydrate-mediated interaction between ERGIC-53 and cathepsin C. We conclude that YFP PCA can detect weak and transient protein interactions in the secretory pathway and hence is a powerful approach to study luminal processes involved in protein secretion. The study extends the application of PCA to carbohydrate-mediated protein-protein interactions of low affinity.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Proteins
  • Carrier Proteins / metabolism
  • Cathepsin K
  • Cathepsin Z
  • Cathepsins / metabolism
  • Fluorescent Antibody Technique
  • Fluorometry
  • Genetic Complementation Test / methods
  • Genetic Vectors
  • HeLa Cells
  • Humans
  • Immunoblotting
  • Luminescent Proteins
  • Mannose-Binding Lectins / metabolism
  • Membrane Proteins / metabolism
  • Protein Engineering
  • Protein Transport / physiology
  • Proteins / metabolism*
  • Transfection
  • Vesicular Transport Proteins

Substances

  • Bacterial Proteins
  • Carrier Proteins
  • LMAN1 protein, human
  • Luminescent Proteins
  • MCFD2 protein, human
  • Mannose-Binding Lectins
  • Membrane Proteins
  • Proteins
  • Vesicular Transport Proteins
  • yellow fluorescent protein, Bacteria
  • Cathepsins
  • CTSZ protein, human
  • Cathepsin Z
  • CTSK protein, human
  • Cathepsin K