scholarly journals 3D-QSAR predictions for bovine serum albumin–water partition coefficients of organic anions using quantum mechanically based descriptors

2017 ◽  
Vol 19 (3) ◽  
pp. 261-269 ◽  
Author(s):  
Lukas Linden ◽  
Kai-Uwe Goss ◽  
Satoshi Endo

The 3D-QSAR model predicts the bovine serum albumin–water partition coefficients for neutral and anionic chemicals influenced by steric effects.

Biochemistry ◽  
1966 ◽  
Vol 5 (8) ◽  
pp. 2606-2616 ◽  
Author(s):  
Ashoka Ray ◽  
Jacqueline A. Reynolds ◽  
Helga Polet ◽  
Jacinto Steinhardt

2019 ◽  
Vol 21 (11) ◽  
pp. 1852-1863 ◽  
Author(s):  
Flora Allendorf ◽  
Urs Berger ◽  
Kai-Uwe Goss ◽  
Nadin Ulrich

Alternatives to long-chain PFAAs sorb similarly strongly to serum albumin as the classical PFAAs.


1970 ◽  
Vol 116 (2) ◽  
pp. 171-175 ◽  
Author(s):  
A. G. Ogston ◽  
Panee Silpananta

1. We have measured the partition coefficients of bovine serum albumin with Sephadex grades G-100, G-150 and G-200, and of a dextran ([unk]n 19700) and a polyethylene glycol ([unk]n 8000) with Sephadex G-200. We have also measured the effects of these solutes on the inner volumes of the grades of Sephadex. 2. The results can be described with fair consistency by means of a simple thermodynamic treatment that makes use of the virial coefficients of Sephadex and of the solute, and of a coefficient that expresses their interaction. This coefficient is related to the ‘exclusion volume’ of Sephadex for the solutes. 3. The Sephadex G-200–polyethylene glycol system shows anomalies of behaviour that are ascribed to the occurrence of ‘incompatible’ phase separation within the Sephadex beads.


Author(s):  
G. D. Gagne ◽  
M. F. Miller

We recently described an artificial substrate system which could be used to optimize labeling parameters in EM immunocytochemistry (ICC). The system utilizes blocks of glutaraldehyde polymerized bovine serum albumin (BSA) into which an antigen is incorporated by a soaking procedure. The resulting antigen impregnated blocks can then be fixed and embedded as if they are pieces of tissue and the effects of fixation, embedding and other parameters on the ability of incorporated antigen to be immunocyto-chemically labeled can then be assessed. In developing this system further, we discovered that the BSA substrate can also be dried and then sectioned for immunolabeling with or without prior chemical fixation and without exposing the antigen to embedding reagents. The effects of fixation and embedding protocols can thus be evaluated separately.


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