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排序方式: 共有806条查询结果,搜索用时 15 毫秒
1.
Andreas Barth 《BBA》2007,1767(9):1073-1101
This review discusses the application of infrared spectroscopy to the study of proteins. The focus is on the mid-infrared spectral region and the study of protein reactions by reaction-induced infrared difference spectroscopy. 相似文献
2.
The objectives of this study were to evaluate the physical structure and the release mechanisms of theophylline microspheres
made of Eudragit S 100 polymer as an enteric polymer, combined with a nonerodible polymer, Eudragit RL 100. In the preparation
process, polymer combinations (1:1) were dissolved in an organic solvent mixture composed of acetone and methanol at a specific
ratio containing a theoretical drug loading of approximately 15%. Two microsphere formulations (LS1 and LS2) were prepared
at two different total polymer concentrations (10% in LS1 and 12.7% in LS2). Dissolution studies were carried out using US
Pharmacopeia Dissolution Apparatus II in an acidic medium for 8 h and in an acidic medium (2 h) followed by a slightly basic-buffered
medium for 10 h. Both LS1 and LS2 microsphere formulations produced particles that were spherical in shape and had very narrow
size distributions with one size fraction comprising 70–80% of the yield. Scanning electron microscopy and quantitative Fourier
transform infrared were used for microsphere physical structure evaluation. Except for the absence of drug crystals, photomicrographs
of both LS microspheres after dissolution in pH 1.2 and 7.2 buffer solutions were similar to those before dissolution. Dissolution
results indicated the ability of LS microspheres to minimize drug release during the acid stage. However, in the slightly
basic medium that followed the acidic stage, the drug release was sustained and controlled in its kinetics and data fitted
to Peppas equation indicated a case II transport suggesting that the drug release is mainly through swelling/erosion mechanism. 相似文献
3.
Fourier transform infrared (FTIR) spectroscopic imaging is an emerging microscopy modality for clinical histopathologic diagnoses as well as for biomedical research. Spectral data recorded in this modality are indicative of the underlying, spatially resolved biochemical composition but need computerized algorithms to digitally recognize and transform this information to a diagnostic tool to identify cancer or other physiologic conditions. Statistical pattern recognition forms the backbone of these recognition protocols and can be used for highly accurate results. Aided by biochemical correlations with normal and diseased states and the power of modern computer-aided pattern recognition, this approach is capable of combating many standing questions of traditional histology-based diagnosis models. For example, a simple diagnostic test can be developed to determine cell types in tissue. As a more advanced application, IR spectral data can be integrated with patient information to predict risk of cancer, providing a potential road to precision medicine and personalized care in cancer treatment. The IR imaging approach can be implemented to complement conventional diagnoses, as the samples remain unperturbed and are not destroyed. Despite high potential and utility of this approach, clinical implementation has not yet been achieved due to practical hurdles like speed of data acquisition and lack of optimized computational procedures for extracting clinically actionable information rapidly. The latter problem has been addressed by developing highly efficient ways to process IR imaging data but remains one that has considerable scope for progress. Here, we summarize the major issues and provide practical considerations in implementing a modified Bayesian classification protocol for digital molecular pathology. We hope to familiarize readers with analysis methods in IR imaging data and enable researchers to develop methods that can lead to the use of this promising technique for digital diagnosis of cancer. 相似文献
4.
5.
Li-Xin Zhang Hou-Guo Liang Jun Wang Wen-Rui Li Tian-Zhi Yu 《Photosynthesis research》1996,48(3):379-384
The 33 kDa protein of Photosystem II has one intrachain disulfide bond. Fluorescence spectroscopy shows that the major groups in the protein that bind to Ca2+ should be the carboxylic side groups of glutamic acid and/or aspartic acid. Fluorescence and Fourier-transform infrared (FTIR) spectroscopic studies indicate that the conformation of the 33 kDa protein is altered upon reduction, while the reduced protein still retains the secondary structure. FTIR spectroscopy also shows that the metal ions induce a relative decrease of unordered structure and -sheet, and a substantial increase of -helix in both the intact and the reduced 33 kDa protein. This indicates that the addition of cations results in a much more compact structure and that both the intact and the reduced 33 kDa proteins have the ability to bind calcium. The above results may suggest that the disulfide bridge is not essential for calcium binding.Abbreviations CD
circular dichroism
- FTIR
Fourier transform infrared
- La
lanthanum
- PS
photosystem
- Tb
terbium 相似文献
6.
7.
Fourier transform infrared spectroscopic study of ion binding and intramolecular interactions in the polar head of digalactosyldiacylglycerol 总被引:2,自引:0,他引:2
Lipid bilayers composed of digalactosyldiacyl-glycerol (DGDG), that is, Galp1-6Galp1-3DAG, a non-ionic lipid of the thylakoid membrane of chloroplasts, aggregate in aqueous media containing mono- and divalent cations in amounts above a threshold concentration (Ct) of about 1.0, 4.7 and 10.0 mM for Ca2+, Mg2+ and Na+, respectively. In this work, we found that above Ct the DGDG membranes do not undergo fusion and that the aggregation can be reversed, or disrupted. This means that the perturbation induced by the salts results from adsorption, or complexation of the ions in the polar head of DGDG. To investigate this question, we used Fourier transform infrared (FTIR) spectroscopy to identify the molecular sites in DGDG which are modified by interaction, or adduct formation with CaCl2, MgCl2 and NaCl. We also determined whether the ions affect the intramolecular hydrogen bonding between the sn2 ester C = O and the carbon-6 of the -anomer of galactose (Gal). The major conclusions are: (i) the salts do not affect, at least directly, the, ester carbonyl region of DGDG, (ii) the most probable sites of binding, or adsorption, for the ions are the ring oxygen, and (iii) the ring hydroxyls are the sites of either ion complexation or intra- and intermolecular H-bonding in interacting DGDG membranes. Within this framework, the complexation of the ions with Gal might induce total or partial dehydration of the galactolipid headgroup and thus provides the means to overcome the repulsive hydration forces that hinder aggregation of the DGDG membranes.Abbreviations DGDG
digalactosyldiacylglycerol
- EDTA
ethylenediaminetetracetic acid
- FTIR
Fourier transform infrared
- Gal
galactose
- GIDG
D-glucosyldiacylglycerol
- Glyc
glycerol
- LHCII
chloroplast light harvesting complex II
- MGDG
monogalactosyldiacylglycerol
- PC
phosphatidylcholine
- PG
phosphatidylglycerol
- PS
phosphatidylserine
- SQDG
sulfoquinovosyl-diacylglycerol
Correspondence to: M. Fragata 相似文献
8.
Establishing isostructural metal substitution in metalloproteins using 1H NMR, circular dichroism, and Fourier transform infrared spectroscopy. 下载免费PDF全文
D. L. Pountney C. J. Henehan M. Vask 《Protein science : a publication of the Protein Society》1995,4(8):1571-1576
Far-UV CD, 1H-NMR, and Fourier transform infrared (FTIR) spectroscopy are three of the most commonly used methods for the determination of protein secondary structure composition. These methods are compared and evaluated as a means of establishing isostructural metal substitution in metalloproteins, using the crystallographically defined rubredoxin from Desulfovibrio gigas and its well-characterized cadmium derivative as a model system. It is concluded that analysis of the FTIR spectrum of the protein amide I resonance represents the most facile and generally applicable method of determining whether the overall structure of a metalloprotein has been altered upon metal reconstitution. This technique requires relatively little biological material (ca. 300 micrograms total protein) and, unlike either CD or 1H-NMR spectroscopy, is unaffected by the presence of different metal ions, thus allowing the direct comparison of FTIR spectra before and after metal substitution. 相似文献
9.
10.
Sadeq K. Alhag Fahd A. Al-Mekhlafi Nael Abutaha Fahd Mohammed Abd Al Galil Muhammad A. Wadaan 《Journal of Asia》2021,24(1):184-189
Plant secondary metabolites have been recently used for the synthesis of different nanoparticles. The present investigation aimed at evaluating the effect of gold (AuNPs) and silver (AgNPs) nanoparticles synthesized using Acalypha fruticosa leaf extracts to control the mosquito Culex pipiens. The A. fruticosa AuNPs and AgNPs spectra displayed their maximum absorption at 550 nm and 440 nm, respectively. The infrared spectra revealed different functional groups related to different chemical compounds. The larval mortality of aqueous leaf extract of A. fruticosa was 499.54 ppm (LC50) and 1734.06 ppm (LC90) after 24 h of treatment. This study revealed that AuNP (LC50, 30.2 and LC90, 104.83 ppm) and AgNP (LC50, 52.86 and LC90, 157.227 ppm) preparations were highly effective compared to the A. fruticosa extract alone and also more affordable, as a smaller amount was required. The present findings show the potential larvicidal effect of the synthesized AuNPs and AgNPs for the control of mosquito-mediated disease transmission. 相似文献