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Covalent linking of photoreactive gonadotropin-releasing hormone to gonadotropes produces a prolonged signal.
Author(s) -
Eli Hazum,
Dana Keinan
Publication year - 1983
Publication title -
proceedings of the national academy of sciences of the united states of america
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.80.7.1902
Subject(s) - covalent bond , gonadotropic cell , receptor , luteinizing hormone , gonadotropin releasing hormone , chemistry , hormone , hormone receptor , biochemistry , derivative (finance) , medicine , endocrinology , biophysics , stereochemistry , biology , organic chemistry , cancer , breast cancer , financial economics , economics
A bioactive, photoreactive derivative of gonadotropin-releasing hormone (GnRH; gonadoliberin), [azidobenzoyl-D-Lys6]GnRH, was shown to bind covalently to dispersed pituitary cells after irradiation. Approximately 7% of the total cell-associated radioactivity was covalently bound to the receptors. Photolysis of cultured pituitary cells in the presence of the photoreactive derivative resulted in persistent activation of luteinizing hormone (LH; lutropin) release. This persistent response was time dependent and concentration dependent. No increase in the basal rate of LH release was observed with cells incubated in the presence of photoreactive GnRH analog and maintained in the dark or with hormone derivatives that lack the photoreactive azido group. These results suggest that only the covalently bound cell surface receptors account for the persistent activation of LH release after photolysis.

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