Literature DB >> 6988266

Radioimmunoassay of chemically modified insulins.

D I Dron, R H Jones, P H Sönksen, J H Thomas, D Brandenburg.   

Abstract

The reactions between four insulin antisera and eighteen insulin derivatives with modifications at the A1, B1 and B29 positions have been studied using a standard double-antibody radioimmunoassay procedure. The derivatives studied had: a) single modifications at A1, B1 or B29,; b) modifications at two sites with or without a crosslink between them; c) modifications at all three sites with or without a crosslink. Analysis of the results showed a clear difference in the reactivity of the antisera. One antiserum (GP5) was highly sensitive to modifications of the B1 residue and another (Ab1) was sensitive to A1 and B29 modifications. Thus, immunological potencies of insulin analogues derived on the basis of these reactions with the antisera give widely varying results. These antisera were used in discriminatory radioimmunoassays of chemically modified insulins in biological fluids for estimation of in vivo hypoglycaemic potencies by an infusion technique, where the knowledge of the specificity of the antisera was useful in assessing the immunological identity of immunoreactive material in plasma with the analogue infused.

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Year:  1980        PMID: 6988266     DOI: 10.1007/BF01228304

Source DB:  PubMed          Journal:  Diabetologia        ISSN: 0012-186X            Impact factor:   10.122


  18 in total

1.  Synthesis and properties of carbonylbis(methionyl)insulin, a proinsulin analogue which is convertible to insulin by cyanogen bromide cleavage.

Authors:  W D Busse; F H Carpenter
Journal:  Biochemistry       Date:  1976-04-20       Impact factor: 3.162

Review 2.  Crosslinked insulins: preparation, properties, and application.

Authors:  D Brandenburg; H G Gattner; W Schermutzki; A Schüttler; J Uschkoreit; J Weimann; A Wollmer
Journal:  Adv Exp Med Biol       Date:  1977       Impact factor: 2.622

3.  Receptor-binding assay of chemically modified insulins. Comparison with in vitro and in vivo bioassays.

Authors:  P Freychet; D Brandenburg; A Wollmer
Journal:  Diabetologia       Date:  1974-02       Impact factor: 10.122

4.  [Preparation and properties of acetyl derivatives of beef insulin. I].

Authors:  D Brandenburg; H G Gattner; A Wollmer
Journal:  Hoppe Seylers Z Physiol Chem       Date:  1972-04

5.  Monosubstituted 2,2-dimethyl-3-formyl-L-thiazolidine-4-carbonyl-insulins.

Authors:  D G Lindsay; S Shall
Journal:  Eur J Biochem       Date:  1970-09

6.  In vitro bioactivity of insulin analogues: lipogenic and anti-lipolytic potency and their interaction with the effect of native insulin.

Authors:  M J Ellis; S C Darby; R H Jones; P H Sönksen
Journal:  Diabetologia       Date:  1978-11       Impact factor: 10.122

7.  Receptor-binding region of insulin.

Authors:  R A Pullen; D G Lindsay; S P Wood; I J Tickle; T L Blundell; A Wollmer; G Krail; D Brandenburg; H Zahn; J Gliemann; S Gammeltoft
Journal:  Nature       Date:  1976-02-05       Impact factor: 49.962

8.  Synthesis of human [9-leucine-B] Insulin.

Authors:  G Schwartz; P G Katsoyannis
Journal:  Biochemistry       Date:  1976-09-07       Impact factor: 3.162

9.  Studies on the relationship between the molecular structure and the catabolism of insulin.

Authors:  D Papachristodoulou; D Brandenburg; D I Dron; R H Jones; P H Sönksen; J H Thomas
Journal:  Acta Biol Med Ger       Date:  1977

10.  Acetoacetylation of insulin.

Authors:  D G Lindsay; S Shall
Journal:  Biochem J       Date:  1969-11       Impact factor: 3.857

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  1 in total

1.  An examination of the role of insulin dimerisation and negative cooperativity using the biological properties of the despentapeptide and deshexapeptide insulins.

Authors:  C S Cockram; R H Jones; P H Sonksen; M A Tatnell; S Q Zhu; G Dodson
Journal:  Diabetologia       Date:  1987-09       Impact factor: 10.122

  1 in total

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