High efficiency acetylcholinesterase immobilization on DNA aptamer modified surfaces
Author(s)
Chumphukam, Orada
Le, Thao T
Cass, Anthony EG
Type
Journal Article
Abstract
We report here the in vitro selection of DNA aptamers for electric eel acetylcholinesterase (AChE). One selected aptamer sequence (R15/19) has a high affinity towards the enzyme (Kd = 157 ± 42 pM). Characterization of the aptamer showed its binding is not affected by low ionic strength (~20 mM), however significant reduction in affinity occurred at high ionic strength (~1.2 M). In addition, this aptamer does not inhibit the catalytic activity of AChE that we exploit through immobilization of the DNA on a streptavidin-coated surface. Subsequent immobilization of AChE by the aptamer results in a 4-fold higher catalytic activity when compared to adsorption directly on to plastic.
Date Issued
2014-04-21
Date Acceptance
2014-04-11
Citation
Molecules, 2014, 19 (4), pp.4986-4996
ISSN
1420-3049
Publisher
MDPI AG
Start Page
4986
End Page
4996
Journal / Book Title
Molecules
Volume
19
Issue
4
Copyright Statement
© 2014 The Author(s). This is an open access article distributed under the Creative Commons Attribution License (CC BY 3.0 - https://creativecommons.org/licenses/by/3.0/).
Sponsor
Biotechnology and Biological Sciences Research Council (BBSRC)
Engineering & Physical Science Research Council (EPSRC)
Identifier
http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000336087800074&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=1ba7043ffcc86c417c072aa74d649202
Grant Number
BB/I001824/1
EP/K039946/1
Subjects
Science & Technology
Life Sciences & Biomedicine
Physical Sciences
Biochemistry & Molecular Biology
Chemistry, Multidisciplinary
Chemistry
aptamers
acetylcholinesterase
immobilization
SINGLE-STRANDED-DNA
PROTEIN-PURIFICATION
MONOVALENT CATIONS
HUMAN THROMBIN
AFFINITY TAGS
MICROARRAYS
RNA
PERFORMANCE
ANTIBODIES
LIGANDS
Publication Status
Published
Date Publish Online
2014-04-21