Selective adenosine-5′-monophosphate uptake by water-compatible molecularly imprinted polymer

被引:33
作者
Breton, Florent [1 ]
Delepee, Raphael [1 ]
Jegourel, Damien [1 ]
Deville-Bonne, Dominique [2 ]
Agrofoglio, Luigi A. [1 ]
机构
[1] Univ Orleans, CNRS, Inst Chim Organ & Analyt, UMR 6005, F-45067 Orleans, France
[2] Univ Paris 06, CNRS, Lab Enzymol Mol & Fonctionnelle, FRE 2852, F-75005 Paris, France
关键词
molecularly imprinted polymer; adenosine monophosphate; boronic acid; water-compatible polymer;
D O I
10.1016/j.aca.2008.04.025
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Molecularly imprinted polymers (MIPs) were prepared for adenosine-5'-monophosphate (AMP), a substrate of AMP-activated protein kinase. The template molecule was formed by the vinylphenylboronate diester of adenosine on which 5'-free hydroxide was protected by tert-butyldimethylsilyl group in order to mimic the steric hindrance of the phosphate moiety of AMP. Molecular imprinting was performed by complexing acrylamide and the template in a highly cross-linked polymer. MIPs were tested in batch experiments with aqueous samples of nucleotides and a number of parameters were investigated. The use of tetrabutylammonium hydroxide (TBAH) was necessary to obtain a rebinding of nucleotides on MIP. The adsorption of AMP was optimal in 5 mM ammonium acetate buffer solution pH 9.5 for 30 min, with 30 mM of TBAH. The imprinted polymer was selective for AMP towards others nucleotides or deoxi analogues. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:222 / 229
页数:8
相关论文
共 34 条
[1]   Molecular imprinting science and technology: a survey of the literature for the years up to and including 2003 [J].
Alexander, C ;
Andersson, HS ;
Andersson, LI ;
Ansell, RJ ;
Kirsch, N ;
Nicholls, IA ;
O'Mahony, J ;
Whitcombe, MJ .
JOURNAL OF MOLECULAR RECOGNITION, 2006, 19 (02) :106-180
[2]  
ARSHADY R, 1981, MACROMOL CHEM PHYS, V182, P687
[3]   Fluorescence sensors for monosaccharides based on the 6-methylquinolinium nucleus and boronic acid moiety: potential application to ophthalmic diagnostics [J].
Badugu, R ;
Lakowicz, JR ;
Geddes, CD .
TALANTA, 2005, 65 (03) :762-768
[4]   A wavelength-ratiometric fluoride-sensitive probe based on the quinolinium nucleus and boronic acid moiety [J].
Badugu, R ;
Lakowicz, JR ;
Geddes, CD .
SENSORS AND ACTUATORS B-CHEMICAL, 2005, 104 (01) :103-110
[5]   INTRACELLULAR METABOLISM AND MECHANISM OF ANTIRETROVIRUS ACTION OF 9-(2-PHOSPHONYLMETHOXYETHYL)ADENINE, A POTENT ANTI-HUMAN-IMMUNODEFICIENCY-VIRUS COMPOUND [J].
BALZARINI, J ;
ZHANG, H ;
HERDEWIJN, P ;
JOHNS, DG ;
DECLERCQ, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (04) :1499-1503
[6]   Binary and ternary phenylboronic acid complexes with saccharides and Lewis bases [J].
Bosch, LI ;
Fyles, TM ;
James, TD .
TETRAHEDRON, 2004, 60 (49) :11175-11190
[7]   The dissociation constants of the chlorophenyl and phenetyl boric acid [J].
Branch, GEK ;
Yabroff, DL ;
Bettman, B .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1934, 56 :937-941
[8]   GENERAL SYNTHESES OF 2',3'-DIDEOXYNUCLEOSIDES AND 2',3'-DIDEHYDRO-2',3'-DIDEOXYNUCLEOSIDES [J].
CHU, CK ;
BHADTI, VS ;
DOBOSZEWSKI, B ;
GU, ZP ;
KOSUGI, Y ;
PULLAIAH, KC ;
VANROEY, P .
JOURNAL OF ORGANIC CHEMISTRY, 1989, 54 (09) :2217-2225
[9]   Molecularly imprinted polymers: synthesis and characterisation [J].
Cormack, PAG ;
Elorza, AZ .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2004, 804 (01) :173-182
[10]   Urea host monomers for stoichiometric molecular imprinting of oxyanions [J].
Hall, AJ ;
Manesiotis, P ;
Emgenbroich, M ;
Quaglia, M ;
De Lorenzi, E ;
Sellergren, B .
JOURNAL OF ORGANIC CHEMISTRY, 2005, 70 (05) :1732-1736