Horm Metab Res 1986; 18(10): 680-685
DOI: 10.1055/s-2007-1012406
ORIGINALS
Basic
© Georg Thieme Verlag, Stuttgart · New York

Radioreceptor Assay for Lactogenic Hormones Based on Membranes from Rat Mammary Tumour

V. G. Pahnke, F. Hoelzel, D. Graesslin, G. Bettendorf
  • Abteilung für klinische und experimentelle Endokrinologie, Universitáts-Frauenklinik Hamburg, Hamburg, Germany
Weitere Informationen

Publikationsverlauf

1984

1985

Publikationsdatum:
14. März 2008 (online)

Summary

A highly sensitive radioreceptor assay (RRA) for human prolactin (hPRL) based on membrane preparations obtained from chemically induced rat mammary tumour is described. The binding of 125I-labelled, highly purified pituitary human prolactin was specific for lactogenic hormones and depending on time, temperature, and concentration of receptor protein. Optimal specific receptor binding (18-20%) was obtained by incubation at 21°C for 18h. The prolactin receptor was shown to have a single “class” of binding sites with an affinity constant (Ka) of 6.0 × 1010 mol-1. The binding capacity was 8-33 fmol/mg membrane protein. The sensitivity of the radioreceptor assay was 0.5 ng/ml ovine prolactin (NIH-PS-10) or 0.84 ng/ml human prolactin (NIH-VLS-4). The receptor binding activity of various purified prolactin preparations from different species was comparable to the biological hormone activities, indicating that this in vitro assay system measures values which are biologically relevant.

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