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xiao猪铁杆木虫 (知名作家)
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一篇最新的综述（nanoparticle–biomolecule systems）
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Biosensors and Bioelectronics Volume 22, Issues 9-10 , 15 April 2007, Pages 1841-1852 Review Integrated nanoparticle–biomolecule systems for biosensing and bioelectronics Itamar Willner，Ronan Baron and Bilha Willner Institute of Chemistry, The Hebrew University of Jerusalem, Jerusalem 91904, Israel Abstract The similar dimensions of biomolecules such as enzymes, antibodies or DNA, and metallic or semiconductor nanoparticles (NPs) enable the synthesis of biomolecule–NP hybrid systems where the unique electronic, photonic and catalytic properties of NPs are combined with the specific recognition and biocatalytic properties of biomolecules. The unique functions of biomolecule–NP hybrid systems are discussed with several examples: (i) the electrical contacting of redox enzymes with electrodes is the basis for the development of enzymatic electrodes for amperometric biosensors or biofuel cell elements. The reconstitution of the apo-glucose oxidase or apo-glucose dehydrogenase on flavin adenine dinucleotide (FAD)-functionalized Au NPs (1.4 nm) associated with electrodes, or on pyrroloquinoline quinone (PQQ)-functionalized Au NPs (1.4 nm) associated with electrodes, respectively, yields electrically contacted enzyme electrodes. The aligned, reconstituted enzymes on the electrode surfaces reveal effective electrical contacting, and the glucose oxidase and glucose dehydrogenase reveal turnover rates of 5000 and 11,800 s−1, respectively. (ii) The photoexcitation of semiconductor nanoparticles yields fluorescence with a wavelength controlled by the size of the NPs. The fluorescence functions of semiconductor NPs are used to develop a fluorescence resonance energy transfer (FRET) assay for nucleic acids, and specifically, for analyzing telomerase activity in cancer cells. CdSe–ZnS NPs are functionalized by a primer recognized by telomerase, and this is elongated by telomerase extracted from HeLa cancer cells in the presence of dNTPs and Texas-red-functionalized dUTP. The dye integrated into the telomers allows the FRET process that is intensified as telomerization proceeds. Also, the photoexcited electron–hole pair generated in semiconductor NPs is used to generate photocurrents in a CdS–DNA hybrid system associated with an electrode. A redox-active intercalator, methylene blue, was incorporated into a CdS–duplex DNA monolayer associated with a Au electrode, and this facilitated the electron transfer between the electrode and the CdS NPs. The direction of the photocurrent was controlled by the oxidation state of the intercalator. (iii) Biocatalysts grow metallic NPs, and the absorbance of the NPs provides a means to assay the biocatalytic transformations. This is exemplified with the glucose oxidase-induced growth of Au NPs and with the tyrosinase-stimulated growth of Au NPs, in the presence of glucose or tyrosine, respectively. The biocatalytic growth of the metallic NPs is used to grow nanowires on surfaces. Glucose oxidase or alkaline phosphatase functionalized with Au NPs (1.4 nm) acted as ‘biocatalytic inks’ for the synthesis of metallic nanowires. The deposition of the Au NP-modified glucose oxidase, or the Au NP-modified alkaline phosphatase on Si surfaces by dip-pen nanolithography led to biocatalytic templates, that after interaction with glucose/AuCl4− or p-aminophenolphosphate/Ag+, allowed the synthesis of Au nanowires or Ag nanowires, respectively. Keywords: Nanoparticles; Enzymes; DNA; Quantum dots; Nanowires; Electrochemistry; Biosensors Article Outline 1. Introduction 2. Electrical wiring of redox enzymes by metal NPs 3. Biomolecule-semiconductor quantum dots for photonic and optoelectronic sensors and devices 4. DNA analysis by metallic NP catalytic labels 5. Biocatalytic growth of metal NPs as enzyme assays 6. The synthesis of nanowires by “biocatalytic inks” and dip-pen nanolithography 7. Conclusions and perspectives [ Last edited by 604gq on 2007-4-10 at 13:38 ] |
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xiao猪
铁杆木虫 (知名作家)
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