Enzyme-Responsive Surfactants for Carbon Nanotubes

Fmoc-peptides are able to disperse otherwise insoluble carbon nanotubes in water

This is a collaboration with Dr Ian Kinloch and Professor Ian Hillier, University of Manchester. We have demonstrated the use of 9-fluorenylmethoxycarbonyl (Fmoc) protected amino acids as cost-effective and versatile surfactants for carbon nanotubes. Quantum mechanical computations were used to model these interactions. These surfactants were then converted into enzymatically activated CNT surfactants which create homogeneous aqueous nanotube dispersions on-demand under constant and physiological conditions.

[1] B.G. Cousins, A.K. Das, R. Sharma, Y. Li, J.P. McNamara, I.H. Hillier, I.A. Kinloch, R.V. Ulijn, Enzymatically Activated Peptide-based Surfactants for Dispersing Carbon Nanotubes, Small, 2009, 5, 587-590.


Liquid Crystal Arrays for Detecting Protease Activity

LCD detection system where enzymes are detected by a amphiphilic Fmoc-peptide cleaved from the N-terminus of a substrate sequence realigns liquid crystals trapped in a TEM grid giving a visible change.

Methods for the parallel screening of protease activity are of great importance, both for activity profiling and in the development of inhibitors. A novel approach to this problem is under development in collaboration with Dr Simon Webb. Our approach involves enzymatic cleavage of peptide surfactants from hydrogel surfaces, whereby the surfactant re-aligns the liquid crystal, resulting to a light to dark transition that is readily observed. Funded by: EPSRC/RSC analytical chemistry.

[1] L.S. Birchall, R.V. Ulijn, S.J. Webb, A Combined SPS-LCD Sensor for Screening Protease Activity, Chem. Commun., 2008, 2861-2863.


Enzyme Triggered Nanoparticle Assembly

Micrographs of gold nanoparticles being dispersed when the adhesive peptide ligans coating their surfaces are hydrolysed by thermolysin.

Nanoparticles are increasingly utilized as core components of biosensors, due to their size- and environment-dependent optical properties. Indeed, colorimetric sensors of high sensitivity have been described for detection of DNA, proteins, enzyme activity, etc. We have, in collaboration with Dr Molly Stevens (Imperial College London) developed a highly sensitive system that makes use of peptide actuators designed to switch from self-assembling to self-repelling upon enzyme action.

[1] A. Laromaine, L. Koh, M. Murugesan, R.V. Ulijn, M.M. Stevens, Enzyme-Triggered Dispersion of Nanoparticle Assemblies, J. Am. Chem. Soc., 2007, 129, 4156-4157.