SYNTHESIS OF 25-HYDROXYVITAMIN-D3 3-BETA-3'-[N-(4-AZIDO-2-NITROPHENYL)AMINO]PROPYL ETHER, A 2ND-GENERATION PHOTOAFFINITY ANALOG OF 25-HYDROXYVITAMIN-D3 - PHOTOAFFINITY-LABELING OF RAT SERUM VITAMIN-D BINDING-PROTEIN

Vulnerability of 25-hydroxy-[26,27-H-3]vitamin D3 3-beta-N-(4-azido-2-nitrophenyl)glycinate, a photoaffinity analogue of 25-hydroxyvitamin D3 (25-OH-D3) (Ray et al., 1986) toward standard conditions of carboxymethylatioin promoted us to synthesize 25-hydroxyvitamin D3 3-beta-3'-[N-(4-azido-2-nitrophenyl)amino]propyl ether (25-ANE), a hydrolytically stable photoaffinity analogue of 25-OH-D3, and 25-hydroxyvitamin D3 3-beta-3'-[N-(4-azido-2-nitro-[3,5-H-3]phenyl)amino]propyl ether (H-3-25-ANE), the radiolabeled counterpart of 25-ANE. Competitive binding assays of 25-OH-D3 and 25-ANE with rat serum demonstrated that 25-ANE competes for the 25-OH-D3 binding site in rat serum vitamin D binding protein (rDBP). On the other hand, UV exposure of a sample of purified rat DBP (rDBP), preincubated in the dark with H-3-25-ANE, covalently labeled the protein. However, very little covalent labeling was observed in the absence of UV light or in the presence of a large excess of 25-OH-D3. These results provide strong evidence for the covalent labeling of the 25-OH-D3 binding site in rDBP by H-3-25-ANE.