Micropatterning proteins on polyhydroxyalkanoate substrates by using the substrate binding domain as a fusion partner

Biotechnol Bioeng. 2005 Oct 20;92(2):160-5. doi: 10.1002/bit.20581.

Abstract

A novel strategy for micropatterning proteins on the surface of polyhydroxyalkanoate (PHA) biopolymer by microcontact printing (microCP) is described. The substrate binding domain (SBD) of the Pseudomonas stutzeri PHA depolymerase was used as a fusion partner for specifically immobilizing proteins on PHA substrate. Enhanced green fluorescent protein (EGFP) and red fluorescent protein (RFP) fused to the SBD could be specifically immobilized on the micropatterns of poly(3-hydroxybutyrate) and poly(3-hydroxybutyrate-co-3-hydroxyhexanoate). Laser scanning confocal microscopic studies suggested that two fusion proteins were micropatterned in their functionally active forms. Also, antibody binding assay by surface plasmon resonance suggested that protein-protein interaction studies could be carried out using this system.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adsorption
  • Binding Sites
  • Carboxylic Ester Hydrolases / analysis
  • Carboxylic Ester Hydrolases / chemistry*
  • Carboxylic Ester Hydrolases / metabolism
  • Carboxylic Ester Hydrolases / ultrastructure*
  • Coated Materials, Biocompatible / analysis
  • Coated Materials, Biocompatible / chemistry*
  • Enzymes, Immobilized / analysis
  • Enzymes, Immobilized / chemistry
  • Enzymes, Immobilized / ultrastructure
  • Materials Testing
  • Polymers / analysis
  • Polymers / chemistry*
  • Polymers / metabolism
  • Protein Binding
  • Pseudomonas stutzeri / enzymology*
  • Pseudomonas stutzeri / genetics
  • Recombinant Fusion Proteins / chemistry*
  • Recombinant Fusion Proteins / metabolism
  • Surface Properties

Substances

  • Coated Materials, Biocompatible
  • Enzymes, Immobilized
  • Polymers
  • Recombinant Fusion Proteins
  • poly(hydroxyethanoate)
  • Carboxylic Ester Hydrolases
  • poly(3-hydroxyalkanoic acid) depolymerase