Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/8284
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Type: Journal article
Title: Measurement of an analog of insulin-like growth factor-I in blood plasma using a novel enzyme-linked immunosorbent assay
Author: Gajanandana, O.
Irvine, K.
Grant, P.
Francis, G.
Knowles, S.
Wrin, J.
Wallace, J.
Owens, P.
Citation: Journal of Endocrinology, 1998; 156(3):407-414
Publisher: J ENDOCRINOLOGY LTD
Issue Date: 1998
ISSN: 0022-0795
1479-6805
Statement of
Responsibility: 
O Gajanandana, K Irvine, PA Grant, GL Francis, SE Knowles, J Wrin, JC Wallace, and PC Owens
Abstract: Long-Arg³-IGF-I (LR³IGF-I) is a synthetic analog of IGF-I that has much lower affinity for IGF-binding proteins than do native IGFs-I and -II. Comparisons of the effects of LR³IGF-I with those of IGFs-I and -II in in vitro and in vivo studies have proved useful in defining the functions of IGF-binding proteins. We have developed a sensitive noncompetitive nonisotopic assay of LR³IGF-I. Mouse IgG 1A7–F5–E5 binds an epitope that contains the substituted arginine³ in LR³IGF-I and was used as the solid phase antibody. The solution phase antibody was a rabbit immunoglobulin Nelson which binds to an epitope that is common to IGF-I and LR³IGF-I. The ELISA system was able to detect as little as 50 pg LR³IGF-I in 100 μl and the native peptides IGFs-I and -II have less than 0•01% activity. Blood plasma from animals treated with pharmacologically active doses of this growth factor analog could be diluted 33•3-fold before assay, at which concentrations plasma had no significant effect on the assay. The ELISA response to LR³IGF-I was unaffected by the presence of IGF-binding proteins. The intra-assay and interassay coefficients of variation are 2•8 and 7•3% respectively. Recovery of LR³IGF-I added to blood plasma was 90%. The ELISA was used to measure LR³IGF-I concentrations in plasma of cows treated with a pharmacologically active dose of this peptide and the results were compared with those obtained by a previously established LR3IGF-I RIA that requires size exclusion chromatography of plasma under acidic conditions to eliminate IGF-binding protein artefacts from the RIA. There was a positive correlation between results obtained by the two assays. The LR³IGF-I ELISA permits discrimination between the exogenous synthetic IGF-I analog and the endogenous native IGFs-I and -II in animals treated with this growth factor without the need for radioiodination of LR³IGF-I and elimination of the requirement for extraction of plasma before assay.
Keywords: Animals
Mice, Inbred BALB C
Cattle
Rabbits
Mice
Hormones
Insulin-Like Growth Factor I
Insulin-Like Growth Factor Binding Proteins
Radioimmunoassay
Enzyme-Linked Immunosorbent Assay
Sensitivity and Specificity
Rights: Copyright © 1998 Journal of Endocrinology Ltd
DOI: 10.1677/joe.0.1560407
Appears in Collections:Aurora harvest
Obstetrics and Gynaecology publications

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