Chemoselective immobilization of proteins by microcontact printing and bio-orthogonal click reactions

Chembiochem. 2013 Dec 16;14(18):2464-71. doi: 10.1002/cbic.201300478. Epub 2013 Oct 25.

Abstract

Herein, a combination of microcontact printing of functionalized alkanethiols and site-specific modification of proteins is utilized to chemoselectively immobilize proteins onto gold surfaces, either by oxime- or copper-catalyzed alkyne-azide click chemistry. Two molecules capable of click reactions were synthesized, an aminooxy-functionalized alkanethiol and an azide-functionalized alkanethiol, and self-assembled monolayer (SAM) formation on gold was confirmed by IR spectroscopy. The alkanethiols were then individually patterned onto gold surfaces by microcontact printing. Site-specifically modified proteins-horse heart myoglobin (HHMb) containing an N-terminal α-oxoamide and a red fluorescent protein (mCherry-CVIA) with a C-terminal alkyne-were immobilized by incubation onto respective stamped functionalized alkanethiol patterns. Pattern formation was confirmed by fluorescence microscopy.

Keywords: chemoselectivity; click chemistry; microcontact printing; protein immobilization; self-assembly.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkanes / chemistry
  • Alkynes / chemistry*
  • Animals
  • Azides / chemistry*
  • Catalysis
  • Click Chemistry / methods*
  • Copper / chemistry
  • Gold / chemistry
  • Horses
  • Immobilized Proteins / chemistry*
  • Luminescent Proteins / chemistry*
  • Myoglobin / chemistry*
  • Oximes / chemistry
  • Red Fluorescent Protein
  • Sulfhydryl Compounds / chemistry*
  • Surface Properties

Substances

  • Alkanes
  • Alkynes
  • Azides
  • Immobilized Proteins
  • Luminescent Proteins
  • Myoglobin
  • Oximes
  • Sulfhydryl Compounds
  • Gold
  • Copper