Protein binding-induced surfactant aggregation variation: a new strategy of developing fluorescent aqueous sensor for proteins

ACS Appl Mater Interfaces. 2015 Mar 4;7(8):4728-36. doi: 10.1021/am508421n. Epub 2015 Feb 18.

Abstract

Novel strategies of developing fluorescent sensors for proteins are highly demanded. In this work, we particularly synthesized a cholesterol-derivatized pyrene probe. Its fluorescence emission is effectively tuned by the aggregation state of a cationic surfactant dodecyltrimethylammonium bromide (DTAB). The used probe/DTAB assemblies exhibit highly sensitive ratiometric responses to pepsin and ovalbumin egg (o-egg) with detection limits of 4.8 and 18.9 nM, respectively. The fluorescence changes indicate the protein-surfactant interaction leads to further aggregation of DTAB assemblies. The results from Tyndall effect and dynamic light scattering verify this assumption. The responses to pepsin and o-egg are due to their strong electrostatic or hydrophobic interaction with DTAB assemblies at pH 7.4. The present noncovalent supramolecular sensor represents a novel and simple strategy for sensing proteins, which is based on the encapsulated fluorophore probing the aggregation variation of the surfactant assemblies.

Keywords: DTAB; pepsin; pyrene; ratiometric sensor; supramolecular assembly.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cholesterol / chemistry
  • Fluorescent Dyes / chemistry
  • Micelles
  • Ovalbumin / analysis*
  • Pepsin A / analysis*
  • Protein Binding
  • Pyrenes / chemistry
  • Quaternary Ammonium Compounds / chemistry
  • Spectrometry, Fluorescence*
  • Surface-Active Agents / chemistry*
  • Water / chemistry

Substances

  • Fluorescent Dyes
  • Micelles
  • Pyrenes
  • Quaternary Ammonium Compounds
  • Surface-Active Agents
  • Water
  • Ovalbumin
  • Cholesterol
  • pyrene
  • Pepsin A
  • dodecyltrimethylammonium