ABSTRACT
A novel SiX-dipropargyl glycerol scaffold (X: H, F, or (18) F) was developed as a versatile prosthetic group that provides technical advantages for the preparation of dimeric radioligands based on silicon fluoride acceptor pre- or post-labeling with fluorine-18. Rapid conjugation with the prosthetic group takes place in microwave-assisted click conjugation under mild conditions. Thus, a bivalent homodimeric SiX-dipropargyl glycerol derivatized radioligand, [(18) F]BMPPSiF, with enhanced affinity was developed by using click conjugation. High uptake of the radioligand was demonstrated in 5-HT1A receptor-rich regions in the brain with positron emission tomography. Molecular docking studies (rigid protein-flexible ligand) of BMPPSiF and known antagonists (WAY-100635, MPPF, and MefWAY) with monomeric, dimeric, and multimeric 5-HT1A receptor models were performed, with the highest G score obtained for docked BMPPSiF: -6.766 as compared with all three antagonists on the monomeric model. Multimeric induced-fit docking was also performed to visualize the comparable mode of binding under in vivo conditions, and a notably improved G score of -8.455 was observed for BMPPSiF. These data directly correlate the high binding potential of BMPPSiF with the bivalent binding mode obtained in the biological studies. The present study warrants wide application of the SiX-dipropargyl glycerol prosthetic group in the development of ligands for imaging with enhanced affinity markers for specific targeting based on peptides, nucleosides, and lipids.
Subject(s)
Brain/diagnostic imaging , Fluorine Radioisotopes/analysis , Glycerol/analogs & derivatives , Organosilicon Compounds/chemistry , Receptor, Serotonin, 5-HT1A/analysis , Animals , Brain/metabolism , Brain Chemistry , Dimerization , Fluorine Radioisotopes/metabolism , Glycerol/chemical synthesis , Glycerol/metabolism , Ligands , Molecular Docking Simulation , Organosilicon Compounds/chemical synthesis , Organosilicon Compounds/metabolism , Positron-Emission Tomography , Rats , Rats, Sprague-Dawley , Receptor, Serotonin, 5-HT1A/metabolismABSTRACT
The methyl transfer reaction from activated monomethyltin, via a modified Stille coupling reaction, was studied under "ligandless" conditions on fully deprotected 5'-modified nucleosides and one dinucleotide. The reaction was optimized to proceed in a few minutes and quantitative yield, even under dilute conditions, thus affording a rapid and efficient new method for oligonucleotide labelling with carbon-11.
Subject(s)
Nucleosides/chemistry , Oligonucleotides/chemistry , Palladium/chemistry , Positron-Emission Tomography/methods , Molecular StructureABSTRACT
Take it eaSi! Nucleosides, dinucleotides, and one oligonucleotide, all modified by click chemistry, have for the first time been directly and very efficiently labeled with (18)F by using a silicon-based, one-step approach that opens the way for the development of a new class of positron emission tomography (PET) tracers (see graphic).
