Direct biomolecule binding on nonfouling surfaces via newly discovered supramolecular self-assembly of lysozyme under physiological conditions

Macromol Biosci. 2012 Aug;12(8):1053-9. doi: 10.1002/mabi.201200092. Epub 2012 Jun 18.

Abstract

When lysozyme is dissolved in a neutral HEPES buffer solution (pH = 7.4) with 0.001-0.050 M TCEP added, a fast phase transition process occurs and the resulting novel fiber-like hierarchical supramolecular assemblies made by primary spherical-particle aggregation can function as a "superglue" that binds strongly and quickly onto non-fouling coatings. This binding is highly selective towards lysozyme, and excludes synthetic, chemical/physical activation/deactivation (blocking) steps. By using biotinylated lysozyme, such a phase transition quickly creates a perfect biotinylated surface on non-fouling surfaces for avidin binding, showing great potential for the development of low-cost and practical biochips.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Avidin / chemistry*
  • Biotin / chemistry*
  • Biotinylation
  • Buffers
  • HEPES
  • Hydrogen-Ion Concentration
  • Immobilized Proteins / chemistry*
  • Muramidase / chemistry*
  • Phase Transition
  • Protein Array Analysis / methods*
  • Solutions
  • Surface Properties

Substances

  • Buffers
  • Immobilized Proteins
  • Solutions
  • Avidin
  • Biotin
  • Muramidase
  • HEPES