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51.
J. Orbán Sz. Halasi G. Papp Szilvia Barkó Beáta Bugyi 《Journal of Thermal Analysis and Calorimetry》2005,82(1):287-290
Summary The thermodynamic properties of the cardiac and skeletal a-actin isoforms were studied to characterize the molecular bases
of the functional differences between them with the method of differential scanning calorimetry (DSC). The thermal properties
of the actin filaments were described in the presence of calcium and magnesium ions as well. Based on the calculated free
energy changes the α-cardiac actin filaments appeared to be more stable in its physiologically more relevant, magnesium saturated
form. The magnesium saturated form of the α-cardiac actin filaments seemed to be more stable compared to the calcium saturated
form of it. The enthalpy and entropy changes could differentiate between the α-cardiac and α-skeletal actin isoforms and between
the calcium and magnesium saturated cardiac actin isoforms as well. Our results can demonstrate that the few differences between
the amino acid sequences of the α-actin isoforms have an influence on the thermal properties and maybe on the function of
these proteins as well. 相似文献
52.
口腔癌系头颈部癌,癌组织均位于口腔内,其非侵入性早期诊断是减少该病死亡的有效手段.唾液系口腔癌变相关物质首先释放进入的体液,取材方便,安全无创,是口腔癌普查筛选、早期诊断的首选指标.本文对唾液肿瘤生物标志物的种类、目前国内外常用的检测方法进行概述,重点阐述新型电化学生物传感方法在口腔癌相关唾液肿瘤生物标志物检测方面的相关应用及其最新研究进展.并对口腔癌相关唾液肿瘤生物标志物电化学传感技术的未来发展方向提出展望,拟为其深入研究与应用提供参考. 相似文献
53.
The extraction and transesterification of soil lipids into fatty acid methyl esters (FAMEs) is a useful technique for studying soil microbial communities. The objective of this study was to find the best solvent mixture to extract soil lipids with a pressurized solvent extractor system. Four solvent mixtures were selected for testing: chloroform:methanol:phosphate buffer (1:2:0.8, v/v/v), chloroform:methanol (1:2, v/v), hexane:2-propanol (3:2, v/v) and acetone. Soils were from agricultural fields and had a wide range of clay, organic matter and microbial biomass contents. Total lipid fatty acid methyl esters (TL-FAMEs) were the extractable soil lipids identified and quantified with gas chromatography and flame ionization detection. Concentrations of TL-FAMEs ranged from 57.3 to 542.2 n mole g−1 soil (dry weight basis). The highest concentrations of TL-FAMEs were extracted with chloroform:methanol:buffer or chloroform:methanol mixtures than with the hexane:2-propanol or acetone solvents. The concentrations of TL-FAMEs in chemical groups, including saturated, branched, mono- and poly-unsaturated and hydroxy fatty acids were assessed, and biological groups (soil bacteria, mycorrhizal fungi, saprophytic fungi and higher plants) was distinguished. The extraction efficiency for the chemical and biological groups followed the general trend of: chloroform:methanol:buffer ≥ chloroform:methanol > hexane:2-propanol = acetone. Discriminant analysis revealed differences in TL-FAME profiles based on the solvent mixture and the soil type. Although solvent mixtures containing chloroform and methanol were the most efficient for extracting lipids from the agricultural soils in this study, soil properties and the lipid groups to be studied should be considered when selecting a solvent mixture. According to our knowledge, this is the first report of soil lipid extraction with hexane:2-propanol or acetone in a pressurized solvent extraction system. 相似文献
54.
W. Russ Algar 《Analytica chimica acta》2010,673(1):1-25
A comprehensive review of the development of assays, bioprobes, and biosensors using quantum dots (QDs) as integrated components is presented. In contrast to a QD that is selectively introduced as a label, an integrated QD is one that is present in a system throughout a bioanalysis, and simultaneously has a role in transduction and as a scaffold for biorecognition. Through a diverse array of coatings and bioconjugation strategies, it is possible to use QDs as a scaffold for biorecognition events. The modulation of QD luminescence provides the opportunity for the transduction of these events via fluorescence resonance energy transfer (FRET), bioluminescence resonance energy transfer (BRET), charge transfer quenching, and electrochemiluminescence (ECL). An overview of the basic concepts and principles underlying the use of QDs with each of these transduction methods is provided, along with many examples of their application in biological sensing. The latter include: the detection of small molecules using enzyme-linked methods, or using aptamers as affinity probes; the detection of proteins via immunoassays or aptamers; nucleic acid hybridization assays; and assays for protease or nuclease activity. Strategies for multiplexed detection are highlighted among these examples. Although the majority of developments to date have been in vitro, QD-based methods for ex vivo biological sensing are emerging. Some special attention is given to the development of solid-phase assays, which offer certain advantages over their solution-phase counterparts. 相似文献
55.
Hojjatollah Nazari Shohreh Azadi Shadie Hatamie Mahsa Soufi Zomorrod Khadijeh Ashtari Masoud Soleimani Simzar Hosseinzadeh 《先进技术聚合物》2019,30(8):2086-2099
The graphene‐based nanocomposites are considered as great candidates for enhancing electrical and mechanical properties of nonconductive scaffolds in cardiac tissue engineering. In this study, reduced graphene oxide‐silver (rGO‐Ag) nanocomposites (1 and 2 wt%) were synthesized and incorporated into polyurethane (PU) nanofibers via electrospinning technique. Next, the human cardiac progenitor cells (hCPCs) were seed on these scaffolds for in vitro studies. The rGO‐Ag nanocomposites were studied by X‐ray diffraction (XRD), Raman spectroscopy, and transmission electron microscope (TEM). After incorporation of rGO‐Ag into PU nanofibers, the related characterizations were carried out including scanning electron microscope (SEM), TEM, water contact angle, and mechanical properties. Furthermore, PU and PU/nanocomposites scaffolds were used for in vitro studies, wherein hCPCs showed good cytocompatibility via 3‐(4, 5‐dimethylthiazol‐2‐yl)‐2,5‐diphenyl tetrazolium bromide (MTT) assay and considerable attachment on the scaffold using SEM studies. Real‐time polymerase chain reaction (PCR) and immunostaining studies confirmed the upregulation of cardiac specific genes including GATA‐4, T‐box 18 (TBX 18), cardiac troponin T (cTnT), and alpha‐myosin heavy chain (α‐MHC) in the PU/rGO‐Ag scaffolds in comparison with neat PU ones. Therefore, these nanofibrous rGO‐Ag–reinforced PU scaffolds can be considered as suitable candidates in cardiac tissue engineering. 相似文献
56.
57.
从长链非编码RNA(long non-coding RNA, lncRNA)与癌细胞生长和代谢的关系角度, 系统地分析和综述了lncRNA如何通过促进或抑制细胞周期进程调节癌细胞生长, lncRNA如何通过调节上皮间质转化影响癌细胞迁移, 以及lncRNA在肿瘤细胞糖类和脂类代谢中如何发挥其作用. 相似文献
58.
O. Pelz C. Hesse M. Tesar R. B. Coffin W.-R. Abraham 《Isotopes in environmental and health studies》2013,49(1-2):131-144
Abstract The δ13C value of bacterial carbon is an important parameter in microbial ecology for studying the carbon flow within a microbial community and for the identification of ecological important strains involved in the mineralization of certain carbon pools in the environment. In our study, biomarkers were isolated from bacteria from a microbial consortium derived from two chemostats and δ13C values were measured. Similar isotope ratios between biomarkers such as fatty acids and outer membrane protein, biomass and substrate were observed. The δ13C analyses of outer membrane protein F of Pseudomonas and biomarker fatty acids were combined to follow bacterial assimilation of 13C labelled 4-chlorocatechol. This new approach was also used in the environment where soil samples were cultivated with different 13C traced substrates. The isotopic analyses of bacterial biomarkers indicated that carbons of histidine were widely incorporated into bacterial biomarkers, in contrast to 4-chlorocatechol which was less often used as a substrate. Results indicate that by isolating bacterial biomarkers and measuring their δ13C values, activities of microbial communities in a complex environmental sample can be determined. This new method has the potential to elucidate individual carbon sources for individual bacterial taxa in microbial ecology. 相似文献
59.
WilliamJ. Griffiths Therese Koal Yuqin Wang Matthias Kohl DavidP. Enot Hans‐Peter Deigner 《Angewandte Chemie (International ed. in English)》2010,49(32):5426-5445
Metabolomics is a truly interdisciplinary field of science, which combines analytical chemistry, platform technology, mass spectrometry, and NMR spectroscopy with sophisticated data analysis. Applied to biomarker discovery, it includes aspects of pathobiochemistry, systems biology/medicine, and molecular diagnostics and requires bioinformatics and multivariate statistics. While successfully established in the screening of inborn errors in neonates, metabolomics is now widely used in the characterization and diagnostic research of an ever increasing number of diseases. In this Review we highlight important technical prerequisites as well as recent developments in metabolomics and metabolomics data analysis with special emphasis on their utility in biomarker identification and qualification, as well as targeted metabolomics by employing high‐throughput mass spectrometry. 相似文献
60.
Chris Petucci Tom Lloyd Heather A. Harris Xiaochun Zhang Vargheese M. Chennathukuzhi Belew Mekonnen Yanxuan Cai 《Journal of mass spectrometry : JMS》2010,45(1):65-71
A sensitive LC/MS/MS method has been developed by derivatization of 17β‐estradiol (E2) with dansyl chloride to quantitate 17β‐E2 in female rat serum. The use of E2‐d5 minimized interferences from endogenous 17β‐E2 in order to achieve a limit of quantitation (LOQ) of 2.5 pg/ml using 150 µl of female rat serum. The recovery of the dansyl derivative was 95% or greater in quality control samples. The intra and interday assay precision was better than 8.2 and 6.2%, respectively, with accuracies ranging from 97 to 101% in the quality control samples. The assay was used for the quantitation of serum E2 as a biomarker for the estrogen receptor (ER) antagonist activity of small molecule SERMs (selective estrogen receptor modulators) in the female rat brain. The study revealed that a statistically significant upregulation of serum 17β‐E2 occurred for rats dosed with SERMs that are known to penetrate the brain and disrupt the hypothalamic‐pituitary‐ovarian (HPO) axis. Variations in 17β‐E2 in ascending dose studies also correlated with the corresponding trends in CYP17a1 levels, an mRNA biomarker for ovarian hyperstimulation. This biomarker assay has provided a useful screen for medicinal chemistry optimization to produce SERMs that do not interfere with negative feedback of estrogens on the brain and for biological hypothesis testing. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献