The influence of aminonucleoside on polysome patterns of rat liver

1970 ◽  
Vol 48 (1) ◽  
pp. 39-43 ◽  
Author(s):  
E. S. Kovacs ◽  
S. D. Kung ◽  
M. A. Moscarello
Keyword(s):  
Size Distribution ◽  
Density Gradient ◽  
Intravenous Injection ◽  
Rat Liver ◽  
Analytical Ultracentrifugation ◽  
Membrane Bound

Intravenous injection of the aminonucleoside of puromycin has been shown to affect the size distribution of polysomes isolated from rat liver. A marked shift to higher aggregates has been observed in both free and membrane-bound polysomes, with a more pronounced shift in the free polysomes. The shift to higher aggregates was observed by both density gradient and analytical ultracentrifugation analyses.

Characterization and Partial Purification of Heterodisperse Polysomal RNAs in Normal and Neoplastic Cells

1972 ◽  
Vol 58 (2) ◽  
pp. 71-94
Author(s):  
Ada Sacchi ◽  
Gianni Chinali ◽  
Susetta Pons ◽  
Michela Galdieri ◽  
Piero Cammarano
Keyword(s):  
Size Distribution ◽  
Density Gradient ◽  
Rat Liver ◽  
Sucrose Density Gradient ◽  
Partial Purification ◽  
Messenger Rnas ◽  
Alkaline Ph ◽  
Sedimentation Profile ◽  
Molecular Weights ◽  
Phenol Extraction

The size distribution of cytoplasmic messenger RNAs (m-RNA) has been studied in rat liver and in monodifferentiated cells (mouse reticulocytes and myelomas). It has been found that the RNA which exhibits a « rapid turnover » and a polydisperse profile of radioactivity is refractory to phenol extraction. This property has been exploited to selectively isolate m–RNA from the phenol residue by means of an extraction at an alkaline pH. The sucrose density gradient profiles of m–RNA isolated from monodifferentiated cells show monodisperse peaks having the sedimentation coefficients expected on the basis of the molecular weights of monocistronic messages for α and β chains of hemoglobin (reticulocytes) and L and H chains of immunoglobulin (myelomas). The sedimentation profile of cytoplasmic m–RNA associated with rat liver polysomes shows a much broader distribution, with sedimentation coefficients ranging from 8 S to 28 S.

Isolation of the 67Gallium Accumulating Fraction in Normal Rat Liver

1974 ◽  
Vol 13 (01) ◽  
pp. 72-84
Author(s):  
K. Hierholzer ◽  
K. zum Winkel ◽  
U. Haubold ◽  
E. Aulbert
Keyword(s):  
Electron Microscopy ◽  
Density Gradient ◽  
Intravenous Injection ◽  
Rat Liver ◽  
Soluble Fraction ◽  
Density Gradient Centrifugation ◽  
Gradient Centrifugation ◽  
Differential Centrifugation ◽  
Normal Rat

SummarySubcellular 67Gallium distribution was investigated in normal rat liver after intravenous injection. By differential centrifugation and density gradient centrifugation 67Gallium accumulating bodies were isolated and identified as lysosomes by enzyme determination and electron microscopy. 67Gallium enrichment in this fraction was 23-fold. Using the isolated 67Gallium accumulating lysosomes the binding state of the isotope inside the lysosomes was studied. 67Gallium was found to be associated with the soluble fraction of lysosomes.

scholarly journals Free and membrane-bound polyribosomes in normal and Rauscher-virus-infected mouse spleen cells

1970 ◽  
Vol 119 (4) ◽  
pp. 749-756 ◽  
Author(s):  
J. Th. M. Burghouts ◽  
A. L. H. Stols ◽  
H. Bloemendal
Keyword(s):  
Density Gradient ◽  
Infected Mouse ◽  
Rat Liver ◽  
Sodium Deoxycholate ◽  
Sucrose Density Gradient ◽  
Spleen Cells ◽  
Ribonuclease Inhibitor ◽  
Rauscher Virus ◽  
Centrifugation Step ◽  
Membrane Bound

1. Free and membrane-bound polyribosomes and ribosomal monomers were isolated from normal and Rauscher-virus-infected mouse spleens by means of discontinuous sucrose density gradients. 2. The addition of ribonuclease inhibitor from rat liver was essential to protect these polyribosomes from degradation. To separate the smooth and rough membranes from ribosomal monomers an additional centrifugation step through a continuous sucrose density gradient was necessary. 3. After infection a marked increase in rRNA from both membrane-bound and free polyribosomes was observed. Treatment of the membrane-bound polyribosomes with sodium deoxycholate yielded only 80S particles even when ribonuclease inhibitor was added. 4. A striking feature of the infected spleen was the occurrence of large polyribosomes. Up to 40 monomers per polyribosome could be counted on electron micrographs.

A Cross-Method Comparison of Sub-10 nm Nanoparticle Size Distribution

2019 ◽  
Author(s):  
Ye Yang ◽  
Suiyang Liao ◽  
Zhi Luo ◽  
Runzhang Qi ◽  
Niamh Mac Fhionnlaoich ◽  
...  
Keyword(s):  
Size Distribution ◽  
Analytical Ultracentrifugation ◽  
Statistical Significance ◽  
Method Comparison ◽  
Size Determination ◽  
Size Dependent ◽  
X Ray Scattering ◽  
Transmission Electron ◽  
Gold Nps ◽  
Reliable Representation

Accurate nanoparticle (NP) size determination is essential across research domains, with many functions in nanoscience and biomedical research being size-dependent. Although transmission electron microscopy (TEM) is capable of resolving a single NP down to the sub-nm scale, the reliable representation of entire populations is plagued by challenges in providing statistical significance, predominantly due to limited sample counts, suboptimal preparation procedures and operator bias during image acquisition and analysis. Meanwhile alternative techniques exist, but reliable implementation requires a detailed understanding of appendant limitations. Herein, conventional TEM is compared to the size determination of sub-10 nm gold NPs in solution by small-angle X-ray scattering and analytical ultracentrifugation. Form-free Monte Carlo fitting of scattering profiles offers access to a direct representation of the core size distribution while ultracentrifugation sedimentation velocity analysis provides information of the hydrodynamic size distribution. We report a comparison of these three methods in determining the size of quasi-monodisperse, polydisperse and bimodal gold nanoparticles of 2 – 7 nm and discuss advantages and limitations of each technique.

scholarly journals Contamination of free-ribosome fractions by detached previously membrane-bound ribosomes (Short Communication)

1974 ◽  
Vol 138 (2) ◽  
pp. 305-307 ◽  
Author(s):  
K. O'Toole
Keyword(s):  
Rat Liver ◽  
Membrane Fraction ◽  
Short Communication ◽  
Free Ribosome ◽  
Membrane Bound ◽  
Free Polyribosome

A rough-membrane fraction isolated from rat liver by a procedure designed to prevent membrane denaturation was subjected to the gradient treatment normally used to isolate free ribosomes. Under these conditions, at most 20% of the ribosomes were detached from membrane with less than 5% sedimenting into the free-polyribosome pellet.

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