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排序方式: 共有485条查询结果,搜索用时 15 毫秒
41.
以四(3,5-二叔丁基-4-羟基苯基丙酸)季戊四醇酯(抗氧剂1010)、Na2SO3作为乙醇胺(MEA)的氧化降解的改性剂,考察改性MEA富集模拟烟道气中CO2的效果,利用气相色谱、红外光谱分析抗氧剂1010与Na2SO3的适宜用量、比较两种抗氧剂的抗氧化性能.结果表明,抗氧剂1010和亚硫酸钠的添加量在0.15%时效... 相似文献
42.
利用能量色散X射线荧光光谱法(energy disperse X-ray fluorescence,EDXRF)对浙江嵊州小黄山与河南舞阳贾湖两处新石器时代前期遗址出土陶器的主量元素化学组成进行了分析测定.结果显示,这两处遗址出土陶器的化学组成地域特征明显,与贾湖遗址相比,小黄山遗址陶器具有我国南方陶瓷器普遍存在的“高... 相似文献
43.
Min JZ Suzuki Y Tomiyasu Y Jin D Higashi T Lee YI Toyo'oka T 《Rapid communications in mass spectrometry : RCM》2011,25(19):2911-2922
With Boc-Asn-GlcNAc as a basic structure, four permanently positively charged kinds of new acceptors (GP-Boc-Asn-GlcNAc, GT-Boc-Asn-GlcNAc, HMP-Boc-Asn-GlcNAc, MPDPZ-Boc-Asn-GlcNAc) and five kinds of similar structure acceptors (2-PA-Boc-Asn-GlcNAc, 3-PA-Boc-Asn-GlcNAc, 4-PA-Boc-Asn-GlcNAc, HP-Boc-Asn-GlcNAc, PDPZ-Boc-Asn-GlcNAc) were synthesized as acceptors for the resolution of oligosaccharides in glycopeptides. The synthesized acceptors enzymatically reacted with Disialo-Asn (donor) in the presence of Endo-M. The reaction yields of each transglycosylation product were not obvious, because we do not have all the authentic Disialo-Asn-Boc-acceptors. Therefore, we used the peak area of the transglycosylation product detected by mass spectrometry and evaluated the utility of each acceptor. Among the Boc-Asn-GlcNAc acceptors, the positively charged MPDPZ derivative peak area was the highest, MPDPZ-Boc-Asn-GlcNAc with a positively charged structure showed about a 2.2 times greater sensitivity of the transglycosylation product compared to the conventional fluorescence acceptor DBD-PZ-Boc-Asn-GlcNAc. As a result, the MPDPZ-Boc-Asn-GlcNAc acceptor was suitable for the transglycosylation reaction with Endo-M. The development of a qualitative determination method for the N-linked oligosaccharides in glycoproteins was attempted by combination of the transglycosylation reaction and semi-micro high-performance liquid chromatography/electrospray ionization quadrupole time-of-flight tandem mass spectrometry (HPLC/ESI-QTOF-MS/MS). The asparaginyl-oligosaccharides in glycoproteins, liberated by treatment with Pronase E, were separated, purified and labeled with positively charged MPDPZ. The resulting derivatives were separated by a semi-micro HPLC system. The eluted N-linked oligosaccharide derivatives were then introduced into a QTOF-MS instrument and sensitively detected in the ESI(+) mode. Various fragment ions based on the carbohydrate units appeared in the MS/MS spectra. Among the peaks, m/z 782.37 corresponding to MPDPZ-Boc-Asn-GlcNAc is the most important one for identifying the asparaginyl-oligosaccharides. Disialo-Asn-Boc-MPDPZ was easily identified by the selected-ion chromatogram at m/z 782.37 by MS/MS detection. Therefore, the identification of N-linked oligosaccharides in glycoproteins seems to be possible by the proposed semi-micro HPLC separations followed by the QTOF-MS/MS detection. Furthermore, several oligosaccharides in ovalbumin and ribonuclease B were successfully identified by the proposed procedure. 相似文献
44.
45.
Khatibisepehr S Huang B Ibrahim F Xing JZ Roa W 《Computational Biology and Chemistry》2011,35(2):69-80
This paper is concerned with dynamic modeling, prediction and analysis of cell cytotoxicity induced by water contaminants. A real-time cell electronic sensing (RT-CES) system has been used for continuously monitoring dynamic cytotoxicity responses of living cells. Cells are grown onto the surfaces of the microelectronic sensors. Changes in cell number expressed as cell index (CI) have been recorded on-line as time series. The CI data are used to develop dynamic prediction models for cell cytotoxicity process. We consider support vector regression (SVR) algorithm to implement data-based system identification for dynamic modeling and prediction of cytotoxicity. Through several validation studies, multi-step-ahead predictions are calculated and compared with the actual CI obtained from experiments. It is shown that SVR-based dynamic modeling has great potential in predicting the cytotoxicity response of the cells in the presence of toxicant. 相似文献
46.
Shen H Wang H Zhou C Niu JZ Yuan H Ma L Li LS 《Dalton transactions (Cambridge, England : 2003)》2011,40(36):9180-9188
Here we report a new "green" method to synthesize Zn(1-x)Cd(x)Se (x = 0-1) and stable red-green-blue tricolor Zn(1-x)Cd(x)Se core/shell nanocrystals using only low cost, phosphine-free and environmentally friendly reagents. The first excitonic absorption peak and photoluminescence (PL) position of the Zn(1-x)Cd(x)Se nanocrystals (the value of x is in the range 0.005-0.2) can be fixed to any position in the range 456-540 nm. There is no red or blue shift in the entire reaction process. Three similar sizes of alloyed Zn(1-x)Cd(x)Se nanocrystals with blue, green, and yellow emissions were successfully selected as cores to synthesize high quality blue, green, and red core/shell nanocrystal emitters. For the synthesis of core/shell nanocrystals with a high quantum yield (QY) and stability, the selection of shell materials has been proven to be very important. Therefore, alternative protocols have been used to optimize thick shell growth. ZnSe/ZnSe(x)S(1-x) and CdS/Zn(1-x)Cd(x)S have been found as an excellent middle multishell to overcoat between the alloyed Zn(1-x)Cd(x)Se core and ZnS outshell. The QYs of the as-synthesized core/shell alloyed Zn(1-x)Cd(x)Se nanocrystals can reach 40-75%. The Cd content is reduced to less than 0.1% for Zn(1 -x)Cd(x)Se core/shell nanocrystals with emissions in the range 456-540 nm. More than 15 g of high quality Zn(1-x)Cd(x)Se core/shell nanocrystals were prepared successfully in a large scale, one-pot reaction. Importantly, the emissions of such thick multishell nanocrystals are not susceptible to ligand loss and stability in various physiological conditions. 相似文献
47.
Efficient delivery of therapeutics into tumor cells to increase the intracellular drug concentration is a major challenge for cancer therapy due to drug resistance and inefficient cellular uptake. Herein, we have designed a tailor-made dual pH-sensitive polymer-drug conjugate nanoparticulate system to overcome the challenges. The nanoparticle is capable of reversing its surface charge from negative to positive at tumor extracellular pH (~6.8) to facilitate cell internalization. Subsequently, the significantly increased acidity in subcellular compartments such as the endosome (~5.0) further promotes doxorubicin release from the endocytosed drug carriers. This dual pH-sensitive nanoparticle has showed enhanced cytotoxicity in drug-resistant cancer stem cells, indicating its great potential for cancer therapy. 相似文献
48.
Ab initio quantum mechanical/molecular mechanical method is combined with the polarized protein-specific charge to study the chemical reactions catalyzed by protein enzymes. Significant improvement in the accuracy and efficiency of free-energy simulation is demonstrated by calculating the free-energy profile of the primary proton transfer reaction in triosephosphate isomerase. Quantitative agreement with experimental results is achieved. Our simulation results indicate that electronic polarization makes important contribution to enzyme catalysis by lowering the energy barrier by as much as 3 kcal/mol. 相似文献
49.
Zhang JZ 《Chemical communications (Cambridge, England)》2011,47(24):6861-6863
This communication demonstrates that improperly formulated data analyses can inflate the strength of statistical correlations and result in drawing incorrect conclusions. The widespread misuse of a second-order kinetic model in the recent literature reveals that many chemists are not aware of the dangers of spurious correlation. 相似文献
50.
Cheng G Zhang JL Liu YL Sun DH Ni JZ 《Chemical communications (Cambridge, England)》2011,47(20):5732-5734
Fe(3)O(4)@SiO(2)@CeO(2) microspheres with magnetic core and mesoporous shell were synthesized, and the multifunctional materials were utilized to capture phosphopeptides and catalyze the dephosphorylation simultaneously, thereby labeling the phosphopeptides for rapid identification. 相似文献