An OsII-bisbipyridine-4-picolinic acid complex mediates the biocatalytic growth of Au nanoparticles:: Optical detection of glucose and acetylcholine esterase inhibition

被引:46
作者
Xiao, Y [1 ]
Pavlov, V [1 ]
Shlyahovsky, B [1 ]
Willner, I [1 ]
机构
[1] Hebrew Univ Jerusalem, Inst Chem, IL-91904 Jerusalem, Israel
关键词
enzymes; gold; inhibitors; nanotechnology; sensors;
D O I
10.1002/chem.200400988
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The complex Os-II-bisbipyridine-4-picolinic acid, [Os(bpy)(2)PyCO2H](2+) (1), mediates the biocatalyzed growth of Au nanoparticles, An NPs, and enables the spectroscopic assay of biocatalyzed transformations and enzyme inhibition by following the An NP plasmon absorbance. In one system, [Os(bpy)(2)PyCO2H](2+) mediates the biocatalyzed oxidation of glucose and the growth of Au NPs in the presence of glucose oxidase, GOx, AuCl4-, citrate and An NP seeds. The mechanism of the Au NPs growth involves the oxidation of the [Os(bpy)(2)PYCO2H](2+) complex by AuCl4- to form [Os(bpy)(2)PyCO2H](3+) and Au-1. The [Os(bpy)(2)PYCO2H](3+) complex mediates the GOx biocatalyzed oxidation of glucose and the regeneration of the mediator 1. Citrate reduces Au-1 and enlarges the An seeds by the catalytic deposition of gold on the Au NP seeds. In the second system, the enzyme acetylcholine esterase, AChE, is assayed by the catalytic growth of the Au NPs. The hydrolysis of acetylcholine (2) by AChE to choline is followed by the [Os(bpy)(2)PYCO2H](3+) mediated oxidation of choline to betaine and the concomitant growth of the Au NPs. The mediated growth of the Au NPs is inhibited by 1,5-bis(4-allyldimethylammonium-phenyl)pentane-3-one dibromide (3). A competitive inhibition process was demonstrated (K-M = 0.13 mm, K-1 = 2.6 mu m) by following the growth of the Au NPs.
引用
收藏
页码:2698 / 2704
页数:7
相关论文
共 51 条
[1]   Sensing of acetylcholine by a tricomponent-enzyme layered electrode using faradaic impedance spectroscopy, cyclic voltammetry, and microgravimetric quartz crystal microbalance transduction methods [J].
Alfonta, L ;
Katz, E ;
Willner, I .
ANALYTICAL CHEMISTRY, 2000, 72 (05) :927-935
[2]  
BARON R, IN PRESS ANAL CHEM
[3]   CHARGE-TRANSFER AND INTRALIGAND ELECTRONIC SPECTRA OF BIPYRIDYL COMPLEXES OF IRON, RUTHENIUM, AND OSMIUM .2. TERVALENT COMPLEXES [J].
BRYANT, GM ;
FERGUSSO.JE .
AUSTRALIAN JOURNAL OF CHEMISTRY, 1971, 24 (02) :275-&
[4]   Raman dye-labeled nanoparticle probes for proteins [J].
Cao, YC ;
Jin, RC ;
Nam, JM ;
Thaxton, CS ;
Mirkin, CA .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (48) :14676-14677
[5]   EFFICACY OF MONO-PYRIDINIUM AND BIS-PYRIDINIUM OXIMES VERSUS SOMAN, SARIN AND TABUN POISONING IN MICE [J].
CLEMENT, JG .
FUNDAMENTAL AND APPLIED TOXICOLOGY, 1983, 3 (06) :533-535
[6]   Inhibition of cholinesterase associated aryl acylamidase activity by anticholinesterase agents: Focus on drugs potentially effective in Alzheimer's disease [J].
Costagli, C ;
Galli, A .
BIOCHEMICAL PHARMACOLOGY, 1998, 55 (10) :1733-1737
[7]   Osmium complexes bearing functional groups: building blocks for integrated chemical systems [J].
Danilowicz, C ;
Corton, E ;
Battaglini, F .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1998, 445 (1-2) :89-94
[8]   DIFFERENTIAL VISUALIZATION OF CHOLINESTERASIC NEURONAL SOMATA AND FIBERS BY USE OF MODIFICATIONS OF ACETYLCHOLINESTERASE PHARMACOHISTOCHEMISTRY [J].
DIPATRE, PL ;
MATHES, CW ;
BUTCHER, LL .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1993, 41 (01) :129-135
[9]   RETARDATION OF NEURITIC OUTGROWTH AND CYTOSKELETAL CHANGES ACCOMPANY ACETYLCHOLINESTERASE INHIBITOR TREATMENT IN CULTURED RAT DORSAL-ROOT GANGLION NEURONS [J].
DUPREE, JL ;
BIGBEE, JW .
JOURNAL OF NEUROSCIENCE RESEARCH, 1994, 39 (05) :567-575
[10]   Evaluation of surface-enhanced resonance Raman scattering for quantitative DNA analysis [J].
Faulds, K ;
Smith, WE ;
Graham, D .
ANALYTICAL CHEMISTRY, 2004, 76 (02) :412-417