scholarly journals The Diamagnetic Susceptibility of the Tubulin Dimer

2014 ◽  
Vol 2014 ◽  
pp. 1-5 ◽  
Author(s):  
Wim Bras ◽  
James Torbet ◽  
Gregory P. Diakun ◽  
Geert L. J. A. Rikken ◽  
J. Fernando Diaz

An approximate value of the diamagnetic anisotropy of the tubulin dimer, Δχdimer, has been determined assuming axial symmetry and that only the α-helices and β-sheets contribute to the anisotropy. Two approaches have been utilized: (a) using the value for the Δχα for an α-helical peptide bond given by Pauling (1979) and (b) using the previously determined anisotropy of fibrinogen as a calibration standard. The Δχdimer≈4×10-27 JT−2 obtained from these measurements are similar to within 20%. Although Cotton-Mouton measurements alone cannot be used to estimate Δχ directly, the value we measured, CMdimer=1.41±0.03×10-8 T−2cm2mg−1, is consistent with the above estimate for Δχdimer. The method utilized for the determination of the tubulin dimer diamagnetic susceptibility is applicable to other proteins and macromolecular assemblies as well.

1976 ◽  
Vol 153 (1) ◽  
pp. 137-138 ◽  
Author(s):  
K W Bentley

Quantitative N-terminal peptide-bond hydrolysis with the cis-beta-hydroxyaquo(triethylenetetramine) cobal (III) ion, i.e. β-[Co(trien)(OH)(OH2)]2+, is reported. The method has been demonstrated with 20 small peptides, a hexapeptide, bradykinin, insulin A chain (oxidized), glucagon and insulin. The procedure involves no acidic hydrolysis step and thus no destruction of labile amino acids.


1983 ◽  
Vol 66 (5) ◽  
pp. 1152-1157
Author(s):  
Arthur Caputi ◽  
Dennis P Mooney ◽  
◽  
J Cherolis ◽  
M Clements ◽  
...  

Abstract After a survey of laboratories using gas chromatographic procedures for wine alcohol analysis, 3 sets of columns and operating parameters were chosen on the basis of comparative reproducibility evaluations run in this laboratory. Fourteen collaborators participated in the study and were given their choice of any one of the 3 columns: (1) 1.8 m × 2 mm id glass, packed with 80-100 mesh Poropak QS; (2) 1.8 m × 2 mm id glass, packed with 0.2% Carbowax 1500 on 80-100 mesh Carbopack C; (3) 1.8 m × 6.35 mm copper, packed with 3% Carbowax 600 on 40-60 mesh Chromosorb T. Standards and samples were diluted 1:100 with 0.1% v/v n-butanol in water before analysis. Eight samples containing from 7.3 to 23.6% ethanol (v/v) were submitted as randomly coded duplicates along with a calibration standard and a practice sample. Two injections each of the diluted duplicates were made. On the basis of the reported results, 2 laboratories were rejected as outliers. The results of the remaining 12 collaborators showed an average reproducibility of 0.142 and a repeatability of 0.036. The method has been adopted official first action.


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