Enzyme reactions in nanoporous, picoliter volume containers

Anal Chem. 2012 Jan 17;84(2):1092-7. doi: 10.1021/ac202726n. Epub 2011 Dec 27.

Abstract

Advancements in nanoscale fabrication allow creation of small-volume reaction containers that can facilitate the screening and characterization of enzymes. A porous, ∼19 pL volume vessel has been used in this work to carry out enzyme reactions under varying substrate concentrations. Assessment of small-molecule and green fluorescent protein diffusion from the vessels indicates that pore sizes on the order of 10 nm can be obtained, allowing capture of proteins and diffusive exchange of small molecules. Glucose oxidase and horseradish peroxidase can be contained in these structures and diffusively fed with a solution containing glucose and the fluorogenic substrate amplex red through the engineered nanoscale pore structure. Fluorescent microscopy was used to monitor the reaction, which was carried out under microfluidic control. Kinetic characteristics of the enzyme (K(m) and V(max)) were evaluated and compared with results from conventional scale reactions. These picoliter, nanoporous containers can facilitate quick determination of enzyme kinetics in microfluidic systems without the requirement of surface tethering and can be used for applications in drug discovery, clinical diagnostics, and high-throughput screening.

Publication types

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

MeSH terms

  • Catalysis
  • Cell Physiological Phenomena
  • Enzymes, Immobilized
  • Glucose / metabolism*
  • Glucose Oxidase / chemistry
  • Glucose Oxidase / metabolism*
  • Horseradish Peroxidase / chemistry
  • Horseradish Peroxidase / metabolism*
  • Humans
  • Hydrogen Peroxide / metabolism*
  • Hydrogen-Ion Concentration
  • Kinetics
  • Microscopy, Fluorescence
  • Nanostructures
  • Nanotechnology*
  • Porosity

Substances

  • Enzymes, Immobilized
  • Hydrogen Peroxide
  • Glucose Oxidase
  • Horseradish Peroxidase
  • Glucose