Picture of neon light reading 'Open'

Discover open research at Strathprints as part of International Open Access Week!

23-29 October 2017 is International Open Access Week. The Strathprints institutional repository is a digital archive of Open Access research outputs, all produced by University of Strathclyde researchers.

Explore recent world leading Open Access research content this Open Access Week from across Strathclyde's many research active faculties: Engineering, Science, Humanities, Arts & Social Sciences and Strathclyde Business School.

Explore all Strathclyde Open Access research outputs...

The past and future of enzyme measurements using surface enhanced Raman spectroscopy

Larmour, Iain A. and Faulds, Karen and Graham, Duncan (2010) The past and future of enzyme measurements using surface enhanced Raman spectroscopy. Chemical Science, 1 (2). pp. 151-160. ISSN 2041-6520

[img]
Preview
Text (Larmour-etal-CS-2010-The-past-and-future-of-enzyme-measurements-using-surface)
Larmour_etal_CS_2010_The_past_and_future_of_enzyme_measurements_using_surface.pdf - Accepted Author Manuscript

Download (1MB) | Preview

Abstract

The ability to accurately and sensitively measure the activity of specific enzymes is central to many aspects of modern chemistry and when combined with new nanoscience based approaches, offers significant opportunities for advancing other scientific disciplines. We review the development of surface enhanced resonance Raman scattering (SERRS) for the detection of enzymes, from the initial direct spectroscopy of enzymes, substrate/product and inhibitors adsorbed onto metallic colloids, to the current approach of measuring enzymatic activity by recording the SERRS spectra of a product which is only 'switched on' after enzyme activity. Developments focussed on improvements to modular masked SERRS substrates, which are unmasked by specific enzymes, are also reviewed. Finally, we set out the remaining grand challenges within the area of enzymatic analysis by SERRS which include single molecule detection, in vivo studies and increased multiplexing for screening of evolved enzyme libraries.