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In vitro interaction of fenretinide with plasma retinol‐binding protein and its functional consequences
Author(s) -
Berni Rodolfo,
Formelli Franca
Publication year - 1992
Publication title -
febs letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.593
H-Index - 257
eISSN - 1873-3468
pISSN - 0014-5793
DOI - 10.1016/0014-5793(92)81046-o
Subject(s) - fenretinide , retinol binding protein , retinoid , transthyretin , retinol , chemistry , plasma protein binding , in vitro , binding protein , blood proteins , retinol binding protein 4 , biochemistry , endocrinology , vitamin , retinoic acid , biology , insulin , adipokine , gene , insulin resistance
The synthetic retinoid fenretinide (4‐HPR; N ‐[4‐hydroxyphenyl] all‐ trans ‐retinamide) interacts with plasma apo‐retinol‐binding protein (RBP)to form a tight complex (λ H J = 0.2 μM) which does not exhibit binding affinity to transthyretin (TTR). Therefore, a substantial modification of the retinol hydroxyl group does not appear to affect the interaction with RBP but does drastically interfere with the protein—protein recognition. The remarkable early reduction in plasma retinol level induced by fenretinide administration may be associated with the high binding affinity of this retinoid to RBP and to its interference with the RBP—TTR complex formation.

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