scholarly journals MOLECULAR WEIGHT AND ELECTROPHORESIS OF CRYSTALLINE RIBONUCLEASE

1940 ◽  
Vol 24 (2) ◽  
pp. 203-211 ◽  
Author(s):  
Alexandre Rothen

Electrophoretic studies on purified crystalline ribonuclease showed the absence of any impurities differing in mobility from the bulk of material. The isoelectric point of ribonuclease was found by electrophoresis to be at about pH 7.8. Ultracentrifuge studies indicated fair homogeneity of ribonuclease in solution. Only one moving component has been observed. The molecular weight of ribonuclease was found to be 12,700 from rate of sedimentation (S25 = 1.85 x 10–13 in 0.5 M (NH4)2SO4) and diffusion measurement (D = 1.36 x 10–6 in 0.5 M (NH4)2SO4), in good agreement with the average value of 13,000 found from equilibrium measurements. This low value for the molecular weight of a protein would seem to discredit the value 17,600 as representing a universal unit weight for proteins in general.

1935 ◽  
Vol 19 (1) ◽  
pp. 95-108 ◽  
Author(s):  
Michael Heidelberger ◽  
Kai O. Pedersen

1. The sedimentation constant of hog thyroglobulin is 19.2ċ10–13. That of human thyroglobulin is essentially the same. 2. The specific volume of hog thyroglobulin is 0.72. 3. The isoelectric point of native hog thyroglobulin is at pH 4.58, that of denatured thyroglobulin at pH 5.0. 4. The molecular weight of hog thyroglobulin is, in round numbers, 700,000, as calculated from the sedimentation and diffusion constants, or 650,000, as calculated from the sedimentation equilibrium data. 5. The thyroglobulin molecule deviates markedly from the spherical.


1993 ◽  
Vol 70 (03) ◽  
pp. 438-442 ◽  
Author(s):  
B Grøn ◽  
C Filion-Myklebust ◽  
S Bjørnsen ◽  
P Haidaris ◽  
F Brosstad

SummaryFibrinogen and fibrin related chains in reduced human plasma as well as the bonds interlinking partially cross-linked fibrin from plasma clots have been studied by means of 1D- and 2D electrophoresis and Western blotting. Immunovisualization of reduced plasma or partially cross-linked fibrin with monoclonal antibodies specific for the α-chains or the γ-chains have shown that several bands represent material belonging to both chains. In order to decide whether these bands constitute αγ-chain hybrids or superimposed α- and γ-chain dimers, the cross-linked material was separated according to both isoelectric point (pI) and molecular weight (MW) using Pharmacia’s Multiphor II system. Western blotting of the second dimension gels revealed that partially cross-linked fibrin contains αsγt-chain hybrids and γ- polymers, in addition to the well-known γ-dimers and α-polymers. The main αsγt-chain hybrid has a pI between that of the α- and the γ-chains, a MW of about 200 kDa and contains Aα-chains with intact fibrinopeptide A (FPA). It was also observed that soluble fibrinogen/fibrin complexes as well as partially cross-linked fibrin contain degraded α-dimers with MWs close to the γ-dimers. These findings demonstrate that factor XIII-catalyzed cross-linking of fibrin is a more complex phenomenon than earlier recognized.


1982 ◽  
Vol 14 (4-5) ◽  
pp. 253-256
Author(s):  
N Sriramula ◽  
M Chaudhuri

An investigation was undertaken on the removal of a model virus, bacterial virus MS2 against Escherichia coli, by sand filtration using untreated, and alum or cationic polyelectrolyte treated media, and uncoagulated as well as alum coagulated influent. Data on discrete virus removal were satisfactorily accounted for by electrokinetic phenomena and diffusion. For virus in association with turbidity, filter coefficients computed from experimental data were in good agreement with those predicted by mechanical straining and gravity settling which were the dominant mechanisms for removal of the turbidity particles to which the viruses attached.


Polymers ◽  
2021 ◽  
Vol 13 (14) ◽  
pp. 2243
Author(s):  
Jiali Qu ◽  
Yi Gao ◽  
Wantai Yang

In this paper, we developed a reactive molecular dynamics (RMD) scheme to simulate the Self-Stable Precipitation (SP) polymerization of 1-pentene and cyclopentene (C5) with maleic anhydride (MAn) in an all-atom resolution. We studied the chain propagation mechanism by tracking the changes in molecular conformation and analyzing end-to-end distance and radius of gyration. The results show that the main reason of chain termination in the reaction process was due to intramolecular cyclic entanglement, which made the active center wrapped in the center of the globular chain. After conducting the experiment in the same condition with the simulation, we found that the distribution trend and peak value of the molecular-weight-distribution curve in the simulation were consistent with experimental results. The simulated number average molecular weight (Mn) and weight average molecular weight (Mw) were in good agreement with the experiment. Moreover, the simulated molecular polydispersity index (PDI) for cyclopentene reaction with maleic anhydride was accurate, differing by 0.04 from the experimental value. These show that this model is suitable for C5–maleic anhydride self-stable precipitation polymerization and is expected to be used as a molecular weight prediction tool for other maleic anhydride self-stable precipitation polymerization system.


1938 ◽  
Vol 21 (3) ◽  
pp. 335-366 ◽  
Author(s):  
John H. Northrop

1. A method for isolating a nucleoprotein from lysed staphylococci culture is described. 2. It is homogeneous in the ultracentrifuge and has a sedimentation constant of 650 x 10–13 cm. dyne–1 sec.–1, corresponding to a molecular weight of about 300,000,000. 3. The diffusion coefficient varies from about 0.001 cm.2/day in solutions containing more than 0.1 mg. protein/ml. to 0.02 in solutions containing less than 0.001 mg. protein/ml. The rate of sedimentation also decreases as the concentration decreases. It is suggested, therefore, that this protein exists in various sized molecules of from 500,000–300,000,000 molecular weight, the proportion of small molecules increasing as the concentration decreases. 4. This protein is very unstable and is denatured by acidity greater than pH 5.0, by temperature over 50°C. for 5 minutes. It is digested by chymo-trypsin but not by trypsin. 5. The loss in activity by heat, acid, and chymo-trypsin digestion is roughly proportional to the amount of denatured protein formed under these conditions. 6. The rate of diffusion of the protein is the same as that of the active agent. 7. The rate of sedimentation of the protein is the same as that of the active agent. 8. The loss in activity when susceptible living or dead bacteria are added to a solution of the protein is proportional to the loss in protein from the solution. Non-susceptible bacteria remove neither protein nor activity. 9. The relative ultraviolet light absorption, as determined directly, agrees with that calculated from Gates' inactivation experiments in the range of 2500–3000 Å. u. but is somewhat greater in the range of 2000–2500 Å. u. 10. Solubility determinations showed that most of the preparations contained at least two proteins, one being probably the denatured form of the other. Two preparations were obtained, however, which had about twice the specific activity of the earlier ones and which gave a solubility curve approximating that of a pure substance. 11. It is suggested that the formation of phage may be more simply explained by analogy with the autocatalytic formation of pepsin and trypsin than by analogy with the far more complicated system of living organisms.


1998 ◽  
Vol 76 (7) ◽  
pp. 559-566 ◽  
Author(s):  
P Singh ◽  
M S Khan ◽  
H Khushnood

Total disintegration events produced in 4.5 A GeV/c 12C--AgBr reactions are analysed to investigate the characteristics of secondary charged particles produced in such collisions. The results reveal that multiplicity distributions of grey, black, and relativistic charged particles agree with the Poisson distribution. The average multiplicity of grey particles is found to increase with the increasing mass of projectile, while the average value of black particles is found to decrease with the increasing mass of projectile. This result is in good agreement with the prediction of fireball model. Finally, the linear dependence of grey and compound multiplicities on black, heavy, and relativistic charged particles is also observed. PACS No.: 25.70


1953 ◽  
Vol 26 (3) ◽  
pp. 655-673 ◽  
Author(s):  
A. G. Veith

Abstract The nonrubber content of typical samples of all grades of technically classified rubber has been determined. It is found that the nonrubber content increases in the order: red, yellow, and blue. The chemical analyses performed to determine the nonrubber content were as follows: per cent ash, per cent nitrogen, per cent acetone extract, and per cent fatty acid. The pH of both a slurry of the ash and the aqueous digest indicates that blue rubber is more basic in these respects than are red and yellow rubbers. The measurement of the cure rate of these samples of technically classified rubber has been carried out by means of (1) conventional stress-strain testing, (2) the present ASTM method utilizing the Mooney viscometer, (3) the National Bureau of Standards strain test, (4) a new and more quantitative approach developed by Gee and coworkers, and (5) a utilization of the Mooney viscometer to determine two of the parameters of Gee's equation which gives the time dependence of modulus. All of these methods place the rubbers in the same relative order. The use of the viscometer to determine two of the parameters of Gee's equation was prompted by the degree of correlation between the rate parameter obtained with the present ASTM method and the rate constant k calculated by Gee's methods. As a result of a preliminary investigation as to the causes of viscosity increases at curing temperatures, it was found that, within limits of experimental error, all of the viscosity increase is due to the formation of a cross-linked network, with a linear relationship existing between viscosity increase ΔVc and modulus (at 100 per cent elongation) f. The results of a comparison of the rate constants obtained by the viscometer and by Gee's method indicate that for MBT mixes at 260° F there is good agreement between the methods. Statistical analysis shows that the samples employed for this study are significantly different in their rate of cure. The variance, range, and mean of some of the parameters obtained with the viscometer over a 10-week period are also given. It is suggested that the Mooney viscometer be employed to classify natural rubber according to its cure rate. If this is done, it will be necessary to define the degree of accuracy desired. To determine accurately the cure rate, it is necessary that the viscometer be used in conjunction with a press cure for the estimation of the parameter f∞. If it is not feasible to carry out press cures, an average value for f∞ can be assumed, and then only a short time test with the viscometer is required.


2015 ◽  
Vol 11 (8) ◽  
pp. 3866-3872
Author(s):  
E.A. Masimov ◽  
Etibar Hummat Ismailov ◽  
S.Y. Odzhaqverdiyeva

Dynamic light scattering (DLS) method in combination with the UV/VIS spectrophotometry is used to study the interaction of polyethylene- glycols with a molecular weight  6000 ( PEG6000 ) with sodium salts of citric and succinic acids in aqueous solutions. The values of density, viscosity, refractive and diffusion indexes, the values of the hydrodynamic diameter, wavelength electronic absorption bands for PEG6000 aqueous solutions, their mixtures with succinic and citric acids are determined. It was shown that depending on the composition of the solutions the values of hydrodynamic diameter for aqueous solutions containing 1-5 wt.% PEG6000 and their mixtures with succinic and citric acids (~ 1 wt%) ranges from 3.6 to 5.2 nm. It is assumed that the formation of complexes with the sizes  that are within the above range is due to the features of interaction  and the structure of the complexes formed in solution.


Author(s):  
V. P. Ustinov ◽  
E. L. Baranova ◽  
K. N. Visheratin ◽  
M. I. Grachev ◽  
A. V. Kalsin

The results of systematic (2003–2017) measurements of the total content and the volume mixing ratio of CO at Novolazarevskaya station with a spectrometer with a resolution of 0.2 cm– 1 are presented. The inverse problem of determining the total CO content, as well as interfering gases (H2O and N2O), was solved using the SFIT4 software package. Data analysis showed that over the measurement period the average total CO content at Novolazarevskaya amounted to (8 ± 2) 1017 molec/cm2, and the average volume mixing ratio amounted to (37 ± 8) ppb. The obtained data are compared with variations in the total content of CO in Arrival-Heights station, with MOPITT satellite data, as well as with surface values of CO concentration at Syova station. The maximum values of CO are observed in September, the minimum — in January–February. For all the considered series, the trends are insignificant, while there are periods of increased CO content (2010). In recent years (2014–2017) there is a tendency towards an increase in the minimum values of CO. For  Novolazarevskaya and  Arrival-Heights satellite data are characterized by the excess of over ground data, amounting to 19% and 14%, respectively, while there is a seasonal dependence of the deviation with the minimum in December–January. Surface measurements of the total CO content are in fairly good agreement at Novolazarevskaya and Arrival-Heights, and since 2010 the average deviation is 2.4%. The average value of the concentration of CO on Syova 51 ppb is higher than the average volume mixing ratio at Novolazarevskaya. According to the spectral, wavelet and composite analyzes, in all the considered series there are oscillations in the range of 6–45 months with closely coinciding periods and phases.


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