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Antibody mimetic receptor proteins for label-free biosensors

Raina, M, Sharma, R, Deacon, Sarah E., Tiede, C, Tomlinson, D, Davies, AG, McPherson, MJ and Walti, C (2014) Antibody mimetic receptor proteins for label-free biosensors. Analyst, 140. pp. 803-810. ISSN 0003-2654

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Abstract

The development of high sensitivity biosensors, for example for clinical diagnostics, requires the
identification of suitable receptor molecules which offer high stability, specificity and affinity, even when
embedded into solid-state biosensor transducers. Here, we present an electrochemical biosensor
employing small synthetic receptor proteins (Mw < 15 kDa) which emulate antibodies but with improved
stability, sensitivity and molecular recognition properties, in particular when immobilized on a solid
sensor surface. The synthetic receptor protein is a non-antibody-based protein scaffold with variable
peptide regions inserted to provide the specific binding, and was designed to bind anti-myc tag antibody
(Mw � 150 kDa), as a proof-of-principle exemplar. Both the scaffold and the selected receptor protein
were found to have high thermostability with melting temperatures of 101 �C and 85 �C, respectively.
Furthermore, the secondary structures of the receptor protein were found to be very similar to that of
the original native scaffold, despite the insertion of variable peptide loops that create the binding sites. A
label-free electrochemical sensor was fabricated by functionalising a microfabricated gold electrode
with the receptor protein. A change in the phase of the electrochemical impedance was observed when
the biosensor was subjected to anti-myc tag antibodies at concentrations between 6.7 pM and 6.7 nM.
These findings demonstrate that these non-antibody receptor proteins are excellent candidates for
recognition molecules in label-free biosensors.

Item Type: Article
Subjects: Q Science > Q Science (General)
R Medicine > R Medicine (General)
Schools: Huddersfield Business School
Depositing User: Sarah Deacon
Date Deposited: 20 Oct 2016 13:54
Last Modified: 04 Dec 2016 03:20
URI: http://eprints.hud.ac.uk/id/eprint/29680

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