UCL Discovery
UCL home » Library Services » Electronic resources » UCL Discovery

Nanopore-Based Electrical and Label-Free Sensing of Enzyme Activity in Blood Serum

Kukwikila, M; Howorka, S; (2015) Nanopore-Based Electrical and Label-Free Sensing of Enzyme Activity in Blood Serum. Anal Chem , 87 (18) pp. 9149-9154. 10.1021/acs.analchem.5b01764. Green open access

[thumbnail of acs.analchem.5b01764.pdf]
Preview
Text
acs.analchem.5b01764.pdf

Download (1MB) | Preview

Abstract

A generic strategy to expand the analytical scope of electrical nanopore sensing is presented. We specifically and electrically detect the activity of a diagnostically relevant hydrolytic enzyme and remove the analytically harmful interference from the biochemically complex sample matrix of blood serum. Our strategy is demonstrated at the example of the renin protease which is involved in regulation of blood pressure. The analysis scheme exploits a new approach to reduce sample complexity while generating a specific read-out signal. Within a single spin-column (i), the protease cleaves a resin-tethered peptide substrate (ii) which is affinity-purified using the same multifunctional resin to remove interfering blood serum components, followed by (iii) detecting the peptide via electrical nanopore recordings. Our approach is beneficial in several ways. First, by eliminating serum components, we overcome limitations of nanopore sensing when challenging samples lead to membrane instability and a poor signal-to-noise ratio. Second, the label-free sensing avoids drawbacks of currently used radiolabel-immunoassays for renin. Finally, the strategy of simultaneous generation and purification of a signal peptide within a multifunctional resin can very likely be expanded to other hydrolytic enzymes dissolved in any analyte matrix and exploited for analytical read-out methods other than nanopore sensing.

Type: Article
Title: Nanopore-Based Electrical and Label-Free Sensing of Enzyme Activity in Blood Serum
Location: United States
Open access status: An open access version is available from UCL Discovery
DOI: 10.1021/acs.analchem.5b01764
Publisher version: http://dx.doi.org/10.1021/acs.analchem.5b01764
Language: English
Additional information: © 2015 American Chemical Society. This is an open access article published under a Creative Commons Attribution (CC-BY) License, which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.
UCL classification: UCL
UCL > Provost and Vice Provost Offices > UCL BEAMS
UCL > Provost and Vice Provost Offices > UCL BEAMS > Faculty of Maths and Physical Sciences
UCL > Provost and Vice Provost Offices > UCL BEAMS > Faculty of Maths and Physical Sciences > Dept of Chemistry
URI: https://discovery.ucl.ac.uk/id/eprint/1472255
Downloads since deposit
113Downloads
Download activity - last month
Download activity - last 12 months
Downloads by country - last 12 months

Archive Staff Only

View Item View Item