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81.
Maeda E Kataoka M Yatsushiro S Kajimoto K Hino M Kaji N Tokeshi M Bando M Kido J Ishikawa M Shinohara Y Baba Y 《Electrophoresis》2008,29(9):1902-1909
A high-performance determination system for alpha-amylase isoenzyme activities in human plasma involving microchip electrophoresis with a plastic chip was developed. The combination of microchip electrophoresis for substrate and hydrolysate separation and an immunoinhibition method for the differentiation of isoenzyme activities using antihuman salivary amylase (S-AMY) mAb allowed the highly selective determination of amylase isoenzyme (S-AMY and pancreatic amylase (P-AMY)) activities even in a complex matrix such as a crude plasma sample. We used 8-aminopyrene-1,3,6-trisulfonic acid (APTS)-labeled maltohexaose (G6) as a substrate. Amylase in a human plasma sample hydrolyzed APTS-G6 into APTS-maltotriose (G3) and G3, which was measured as the fluorescence intensity of APTS-G3 on microchip electrophoresis. A double logarithm plot revealed a linear relationship between amylase activity and fluorescence intensity in the range of 5-500 U/L of amylase activity (r2=0.9995, p<0.01), and the LOD was 4.38 U/L. Amylase activities in 13 subjects determined by the present method were compared with the results obtained by conventional methods with nitrophenylated oligosaccharides as substrates, respectively. Good correlations were observed for each method on simple linear regression analysis (both p<0.01). The reproducibilities of within-days for total amylase and P-AMY were 2.98-6.27 and 3.83-6.39%, respectively, and these between-days were 2.88-5.66 and 3.64-5.63%, respectively. This system enables us to determine amylase isoenzyme activities in human plasma with high sensitivity and accuracy, and thus will be applicable to clinical diagnosis. 相似文献
82.
Fouad M Jabasini M Kaji N Terasaka K Tokeshi M Mizukami H Baba Y 《Electrophoresis》2008,29(11):2280-2287
We describe a new and selective analytical method for the separation and quantitation of plant glucosinolates. The new method, which utilizes microchip CE (micro-CE) with fluorescence detection, circumvents the multistep procedures characteristic of conventional methods. Glucosinolates form charge transfer complexes with the xanthene dyes phloxine-B and eosin-B. The glucosinolates-phloxine-B complex cannot be excited at 470 nm. Thus, the decrease in peak intensity of phloxine-B after complex formation is used to quantitatively measure total glucosinolates in Arabidopsis thaliana seeds. For qualitative analysis, complex formation with eosin-B is used. The sensitivity of eosin-B detection at excitation/emission 470 nm/540 nm was low. However, sensitivity increased following complex formation with sinigrin (> or =3 microg/mL). A batch-learning, self-organizing map was applied to visualize and organize analytical data into 2-D matrix with similar and related data clustered together or near each other. This organized matrix was used to optimize electrophoretic conditions for the analysis. This study suggests potential applications of micro-CE in plant metabolomics analyses without use of labeling fluorophores. 相似文献
83.
An ordinary atomic force microscopy (AFM) was functionalized and applied to electrochemically draw micropatterns of biomolecules.
To fabricate an electrochemical AFM probe having an electrode at the tip, a metal-coated AFM probe was first insulated with
Parylene C, and then the apex of the tip was ground mechanically to expose the electrode. The effective electrode diameter
was estimated to be ca. 500 nm. The electrode probe was positioned close to a heparin-coated antibiofouling substrate and
used to locally generate hypobromous acid from a dilute Br− solution to render the substrate surface protein-adhesive. In situ topographical imaging after the electrochemical treatment
suggested the heparin layer became detached to allow the adsorption of proteins, in this case fibronectin. The diameter of
the drawn fibronectin pattern was 2 μm, which is one order of magnitude smaller than we achieved previously using a microdisk
electrode (tip diameter 10 μm).
Figure AFM configuration integrated with the electrochemical-based surface modification and resultant micropatterns of fluorescence-labeled
fibronectin
Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users. 相似文献
84.
Kuroda D Zhang Y Wang J Kaji N Tokeshi M Baba Y 《Analytical and bioanalytical chemistry》2008,391(7):2543-2549
A thermo-responsive separation matrix, consisting of Pluronic F127 tri-block copolymers of poly(ethylene oxide) and poly(propylene
oxide), was used to separate DNA fragments by microchip electrophoresis. At low temperature, the polymer matrix was low in
viscosity and allowed rapid loading into a microchannel under low pressure. With increasing temperatures above 25°C, the Pluronic
F127 solution forms a liquid crystalline phase consisting of spherical micelles with diameters of 17–19 nm. The solution can
be used to separate DNA fragments from 100 bp to 1500 bp on poly(methyl methacrylate) (PMMA) chips. This temperature-sensitive
and viscosity-tunable polymer provided excellent resolution over a wide range of DNA sizes. Separation is based on a different
mechanism compared with conventional matrices such as methylcellulose. To illustrate the separation mechanism of DNA in a
Pluronic F127 solution, DNA molecular imaging was performed by fluorescence microscopy with F127 polymer as the separation
matrix in microchip electrophoresis.
Figure Temperature dependence of the viscosity of 20% w/w Pluronic F127 solution in 1xTBE buffer. Dotted approximates resultant curve. 相似文献
85.
Quantitative determination of amino acids in functional foods by microchip electrophoresis 总被引:1,自引:0,他引:1
Microchip electrophoresis (MCE), a first-generation micrototal analysis system, has emerged during the miniaturization phase of food analysis. Based on the micellar electrokinetic chromatography mode, a simple and fast MCE method with light emitting diode-induced fluorescence detection was developed for quantitative analysis of amino acids in three different kinds of functional foods, viz. sports beverages, jelly-form beverages, and tablet-form functional foods. In contrast to the glass microchip, we improved the separation of amino acids on a poly(methyl methacrylate) (PMMA) chip by addition of cationic starch derivatives. 4-fluoro-7-nitro-2,1,3-benzoxadiazole, which has a short labeling time for amino acids, was used as the fluorescently labeled dye. This MCE method takes less than 10 min of total analysis time including sample preparation and analysis of amino acids in functional foods on a PMMA chip. The results show that this approach has the potential to be a fast and simple method for amino acid analysis in functional foods. 相似文献
86.
We developed a novel channel wall coating on a poly(methyl methacrylate) (PMMA) microchip using methylcellulose (MC) as a coating reagent to suppress electroosmotic flow (EOF) following the strong analytes adsorption via hydrophobic interaction with channel walls of PMMA. Our coating was obtained by first rinsing channel walls with MC-containing aqueous solution followed by evaporation. The coating made the hydrophilic channel wall lowering EOF by two orders of magnitude (1.2 x 10(-5)cm(2)V(-1)s(-1)) as well as reducing the hydrophobic adsorption. On the coated channel walls, we successfully separated sodium dodecyl sulfate-protein complexes with high reproducibility and efficiency using dextran as a lower viscosity protein separation medium. 相似文献
87.
We demonstrate channel wall coating using a cellulose derivative on a poly-(methyl methacrylate) (PMMA) CE microchip to eliminate EOF disturbing protein separation. The channel walls were modified by preconditioning with a solution containing the cellulose derivative and then thermally evaporating the solution to produce hydrophilic channel walls which prevent adsorption of analytes via a hydrophobic interaction. When the PMMA substrate was coated with the cellulose derivative hydroxypropylmethylcellulose (HPMC) 90SH, the water contact angle on the coated substrate was decreased (up to 15 degrees ) and EOF was significantly suppressed (up to 4.0 x 10(-6) cm2.V(-1)s(-1)). Three proteins (20.5, 68.0, and 114.6 kDa) were successfully separated on the 0.15% HPMC 90SH-coated channel walls with good reproducibility of migration time (RSD <1.75%) and high efficiency (theoretical plate number per meter: 2.62 x 10(5)). 相似文献
88.
Nishizawa M Kamiya T Nozaki H Kaji H 《Langmuir : the ACS journal of surfaces and colloids》2007,23(16):8304-8307
We have studied the possibility of making biocompatible, conductive patterns on a substrate by controlling the lateral growth rate of conducting polymers upon electropolymerization. Surface modification with heparin was found to enhance the lateral growth of polypyrrole, especially in the presence of dodecylbenzenesulfonate, and thus the micropatterning of heparin around electrodes leads to the formation of polypyrrole patterns. 相似文献
89.
Matyja A Rozanska M Adachi I Aihara H Aulchenko V Aushev T Bahinipati S Bakich AM Balagura V Barberio E Bedny I Bhardwaj V Bitenc U Bondar A Bozek A Bracko M Brodzicka J Browder TE Chang MC Chang P Chen A Chen KF Cheon BG Chistov R Cho IS Choi Y Choi YK Dalseno J Dash M Eidelman S Fratina S Gabyshev N Golob B Ha H Haba J Hara T Hayasaka K Hazumi M Heffernan D Hokuue T Hoshi Y Hou WS Hyun HJ Iijima T Ikado K Inami K Ishikawa A Ishino H Itoh R Iwasaki Y Kaji H Kajiwara S Kang JH Katayama N 《Physical review letters》2007,99(19):191807
We report an observation of the decay B{0}-->D{*-}tau{+}nu{tau} in a data sample containing 535x10{6} BB pairs collected with the Belle detector at the KEKB asymmetric-energy e{+}e{-} collider. We find a signal with a significance of 5.2sigma and measure the branching fraction B(B{0}-->D{*-}tau{+}nu{tau})=(2.02{-0.37}{+0.40}(stat)+/-0.37(syst))%. This is the first observation of an exclusive B decay with a b-->ctaunu{tau} transition. 相似文献
90.
Mizuk R Abe K Adachi I Aihara H Anipko D Aulchenko V Aushev T Bakich AM Balagura V Barberio E Bay A Bedny I Belous K Bitenc U Bizjak I Blyth S Bondar A Bozek A Bracko M Brodzicka J Browder TE Chang MC Chen A Chen KF Chen WT Cheon BG Chistov R Choi Y Choi YK Cole S Dalseno J Danilov M Drutskoy A Eidelman S Epifanov D Fratina S Gabyshev N Garmash A Gershon T Gokhroo G Golob B Ha H Haba J Hayasaka K Hayashii H Hazumi M Heffernan D Hokuue T Hoshi Y Hou S Hou WS Iijima T Ikado K Imoto A Inami K 《Physical review letters》2007,98(26):262001
We report the results of several studies of the Lambda(c)(+)pi(+)pi(-)X final state in continuum e(+)e(-) annihilation data collected by the Belle detector. An analysis of angular distributions in Lambda(c)(2880)(+)-->Sigma(c)(2455)(0,++)pi(+,-) decays strongly favors a Lambda(c)(2880)(+) spin assignment of 5/2 over 3/2 or 1/2. We find evidence for Lambda(c)(2880)(+)-->Sigma(c)(2520)(0,++)pi(+,-) decay and measure the ratio of Lambda(c)(2880)(+) partial widths Gamma(Sigma(c)(2520)pi)/Gamma(Sigma(c)(2455)pi)=0.225+/-0.062+/-0.025. This value favors the Lambda(c)(2880)(+) spin-parity assignment of 5/2(+) over 5/2(-). We also report the first observation of Lambda(c)(2940)(+)-->Sigma(c)(2455)(0,++)pi(+,-) decay and measure Lambda(c)(2880)(+) and Lambda(c)(2940)(+) mass and width parameters. These studies are based on a 553 fb(-1) data sample collected at or near the Upsilon(4S) resonance at the KEKB collider. 相似文献