Chromatographic Fractionation and Characterization of Antibody Based on the Thermal Dissociation of the Specific Antigen–Antibody Complex

Nature ◽  
1962 ◽  
Vol 193 (4813) ◽  
pp. 350-353 ◽  
Author(s):  
HAROLD S. GOODMAN
1943 ◽  
Vol 78 (5) ◽  
pp. 327-332 ◽  
Author(s):  
Stuart Mudd ◽  
Ferdinand Heinmets ◽  
Thomas F. Anderson

Electron micrographs indicate, in harmony with previous findings, that the pneumococcal capsule is a gel of low density outside of and closely applied to the bacterial cell wall. Interaction with homologous immune rabbit serum greatly increases the thickness and density of this capsular gel; the increase in thickness of the specifically swollen pneumococcal capsule may exceed by 25-fold the thickness of the surface deposit caused by rabbit immune serum on the cell walls and flagella of homologous non-capsulated bacteria. Conclusions drawn from these and earlier data are that homologous immune serum permeates the pneumococcal capsular gel; the specific antibody combines with the capsular polysaccharide; non-specific serum components are secondarily adsorbed to or combined with the specific antigen-antibody complex. The relatively low antibacterial titers characteristic of pneumococcal antisera can be explained in part by the permeation of the capsule by antiserum, in part by the high combining capacity of pneumococcal carbohydrate for antibody (17).


1982 ◽  
Vol 37 (11-12) ◽  
pp. 1146-1156
Author(s):  
Eva Sepp ◽  
Gerhard Wanner ◽  
Jörg Eder ◽  
Hans-Peter Köst

Abstract Antibodies against phycobilisom es of Porphyridium cruentum immunoreact with B-phycoerythrin from the same organism. A strong antigen-antibody complex is not only formed with the native B-phycoerythrin but also when the chromophore is chemically reduced, split or even degraded with chromic acid. Characteristics of precipitations and dissolutions in the presence of the chaotropic reagents urea and potassium rhodanide are discussed for the immunocomplex with native B-phycoerythrin. A sandwich-type immunoadsorbent column appropriate for antigen-isolation is described; its binding properties are investigated biochem ically and by electron microscopy.


1958 ◽  
Vol 108 (6) ◽  
pp. 891-904 ◽  
Author(s):  
Jonathan W. Uhr ◽  
A. M. Pappenheimer ◽  

Guinea pigs rendered hypersensitive (delayed-type) to protein antigen can be completely and specifically desensitized by a single injection containing a sufficient amount of the corresponding antigen. Although 1 to 2 mg. of specific antigen are required for complete desensitization, as little as 20 µg. suffices to decrease the size of specific skin reactions in sensitized animals. The duration of non-reactivity lengthens as the amount of antigen in the desensitizing injection is increased, but skin reactivity eventually returns and is accompanied by the appearance of excess circulating antibody. Desensitization can be accomplished with the antigen-antibody complex as well as by "free" antigen. The appearance of delayed skin reactions can be prevented in fully sensitized animals by intravenous desensitization 2 or more hours after intradermal challenge or by simply skin testing with a desensitizing dose of specific antigen. Injection of a desensitizing dose of antigen into specifically sensitized animals also results in a transient anergic state, the implications of which are discussed.


Author(s):  
William P. Jollie

A technique has been developed for visualizing antibody against horseradish peroxidase (HRP) in rat visceral yolk sac, the placental membrane across which passive immunity previously has been shown to be transferred from mother to young just prior to birth. Female rats were immunized by injecting both hind foot pads with 1 mg HRP emulsified in complete Freund's adjuvant. They were given a booster of 0.5mg HRP in 0.1 ml normal saline i.v. after one week, then bred and autopsied at selected stages of pregnancy, viz., 12, 1 7 and 22 days post coitum, receiving a second booster, injected as above, five days before autopsy. Yolk sacs were removed surgically and fixed immediately in 2% paraformaldehye, 1% glutaraldehye in 0.1 M phosphate buffer with 0.01% CaCl2 at pH 7.4, room temperature, for 3 hr, rinsed 3X in 0.1 M phosphate buffer plus 5% sucrose, then exposed to 1 mg HRP in 1 ml 0.1 M phosphate buffer at pH 7.4 for 1 hr. They were refixed in aldehydes, as above, for 1 5 min (to assure binding of antigen-antibody complex). Following buffer washes, the tissues were incubated in 3 mg diaminobenzidine tetrahydrochloride and 0.01% H2O2 in 0.05 M Tris-HCl buffer for 30 min. After brief buffer washes, they were postfixed in 2% OsO4. in phosphate buffer at pH 7.4, 4°C for 2 hr, dehydrated through a graded series of ethanols, and embedded in Durcupan. Thin sections were observed and photographed without contrast-enhancement with heavy metals. Cytochemical reaction product marked the site of HRP (i.e., antigen) which, in turn, was present only where it was bound with anti-HRP antibody.


1966 ◽  
Vol 51 (1) ◽  
pp. 88-94 ◽  
Author(s):  
A. Villanueva ◽  
S. J. H. Ashcroft ◽  
J. P. Felber

ABSTRACT The synthetic ACTH peptides β1–39 and β1–24 stimulated lipolysis as determined by the rat epididymal fat pad in vitro. The stimulating effect of these peptides was diminished by prior incubation of the peptides with antibodies produced by the guinea-pig against ACTH. The stimulating effect of these hormones was also diminished by the double antibody system used in the radio-immunoassay of ACTH and other peptide hormones, in which incubation with antiserum is followed by precipitation of the antigen-antibody complex by rabbit anti-guinea-pig-γ-globulin.


1973 ◽  
Vol 71 (4_Suppl) ◽  
pp. S11
Author(s):  
K. Schemmel ◽  
L. Weisbecker ◽  
H. Norden ◽  
V. Mokmol ◽  
V. Becker ◽  
...  

1994 ◽  
Vol 269 (31) ◽  
pp. 20126-20133 ◽  
Author(s):  
G.J. Adema ◽  
A.J. de Boer ◽  
A.M. Vogel ◽  
W.A. Loenen ◽  
C.G. Figdor

Sign in / Sign up

Export Citation Format

Share Document