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Analytical errors in measuring radioactivity in cell proteins and their effect on estimates of protein turnover in L cells. 总被引:1,自引:1,他引:0 下载免费PDF全文
Previous studies from this laboratory on protein turnover in 3H-labelled L-cell cultures have shown recovery of total 3H at the end of a 3-day experiment to be always significantly in excess of the 3H recovered at the beginning of the experiment. In this study we have critically reviewed a number of possible sources for this error in measuring radioactivity in cell proteins. 3H-labelled proteins, when dissolved in 0.3 M-NaOH and counted for radioactivity in a liquid-scintillation spectrometer, showed losses of 30-40% of the radioactivity; neither external or internal standardization compensated for this loss. Hydrolysis of these proteins with either Pronase or concentrated HCl significantly increased the measured radioactivity. In addition, approx. 5-10% of the cell protein is left on the plastic culture dish when cells are recovered in phosphate-buffered saline. To aggravate this latter loss further, this surface-adherent protein, after pulse labelling, contains proteins of high radioactivity that turn over rapidly and make a major contribution to the accumulating radioactivity in the medium. These combined errors can account for up to 60% of the total radioactivity in the cell culture. Similar analytical errors have been found in studies of other cell cultures. The effect of these analytical errors on estimates of protein turnover in cell cultures is discussed. 相似文献
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Macrophage cooperation has been shown to be necessary for the thymus-derived lymphocyte to express many of its differentiated functions. The importance of macrophage-lymphocyte interaction has been extended to the study of nonimmunogenic mitogenesis. Utilizing human macrophages and T-cells prepared separately to greater than 98% purity, we have demonstrated a marked degree of dependence of the T-cell upon the macrophage for mitogenesis in response to phytohemagglutinin. The degree of dependence observed is greater than that seen with other human systems and on the order of that seen in the highly purified nonhuman systems. The nature of the physical interaction between the macrophage and the T-cell was visualized using conventional light microscopy and scanning electron microscopy. Lymphocytes were observed to form a semirosetting pattern around the macrophage very early following mitogenic stimulation. The lymphocytes were observed to proceed through early blastogenesis while in direct contact with the macrophage. 相似文献
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Background
Radial chromosome positioning in interphase nuclei is nonrandom and can alter according to developmental, differentiation, proliferation, or disease status. However, it is not yet clear when and how chromosome repositioning is elicited. 相似文献6.
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The biodegradation of an aluminum-bearing (basalt) rock by Penicillium simplicissimum has been investigated. This organism grows on a sugar substrate and releases organic acid compounds. These acids interact with the mineral matter and cause their partial decomposition. The dissolved metals are then complexed by the excess organic acids. The activity of the fungi was found to be optimum at an initial pH 7 and in the presence of 5% (w/v) substrate concentration. In 30 days of leaching almost 20% of the aluminum in the rock was solubilized and the pH was decreased from 7 to less than 3.5 in the inoculated flasks. The controls showed less than 1% of the aluminum solubilized and the final pH dropped to only 6.8. A surface characterization study performed by scanning electron microscopy indicated that the specific mineralogical phases containing aluminum and iron within this host rock were preferentially corroded. The mineral phases containing olivine and plagioclase were found to be least resistant, while phases containing titanium were most resistant to the acids released by the fungi. 相似文献
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Removal of a Single α-Tubulin Gene Intron Suppresses Cell Cycle Arrest Phenotypes of Splicing Factor Mutations in Saccharomyces cerevisiae 下载免费PDF全文