| Literature DB >> 27990672 |
Falguni Basuli1, Xiang Zhang1, Carolyn C Woodroofe1, Elaine M Jagoda2, Peter L Choyke2, Rolf E Swenson1.
Abstract
Fluorine-18 labeling of biomolecules is mostly performed by an indirect labeling method using a prosthetic group. Fluorine-18 labeled 6-fluoronicotinic acid-2,3,5,6-tetrafluorophenyl ester is a useful prosthetic group to radiolabel a protein. Recently, we reported an improved preparation of this prosthetic group. To test the conjugation efficiency of the labeled ester prepared by this method, we have performed conjugation reactions with a peptide, a protein, and a small molecule. Prostate-specific membrane antigen targeting small molecule [18 F]DCFPyL, αvβ3 integrin receptors targeting peptide [18 F]c(RGDfK) and [18 F]albumin were prepared in good radiochemical yields. The conjugation reactions were completed at 40°C to 50°C in 10 minutes. The overall radiochemical yield was 25% to 43% in 30 to 45 minutes. Published 2016. This article is a U.S. Government work and is in the public domain in the USA.Entities:
Keywords: F-18; peptide; protein; radiolabeling
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Year: 2017 PMID: 27990672 PMCID: PMC5344719 DOI: 10.1002/jlcr.3487
Source DB: PubMed Journal: J Labelled Comp Radiopharm ISSN: 0362-4803 Impact factor: 1.921