Convenient and Efficient Synthesis of a Lanthanide-Coordinated, Diethylene Triamine Pentaacetic Acid Labeled Biopolymer as an Assay for the Cholecystokinin B Receptor.
Convenient and Efficient Synthesis of a Lanthanide-Coordinated, Diethylene Triamine Pentaacetic Acid Labeled Biopolymer as an Assay for the Cholecystokinin B Receptor.
复制标题
方便高效地合成镧系元素配位、二亚乙基三胺五乙酸标记的生物聚合物,用于胆囊收缩素 B 受体的测定。
DOI:
10.1002/app.26910
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发表时间:
2007
期刊:
影响因子:
--
通讯作者:
Gillies,R
中科院分区:
文献类型:
--
作者:
Gao,F;Handl,H;Vagner,J;Hruby,V;Gillies,R
To develop an assay for the cholecystokinin B receptor with an Eu3+‐labeled cholecystokinin peptide via a diethylene triamine pentaacetic acid chelating linker, a commercial dianhydride diethylene triamine pentaacetic acid precursor was directly attached to the N‐terminus of cholecystokinin peptides by a solid‐phase synthesis method with a satisfactory yield and purity after reverse‐phase high‐performance liquid chromatography separation. Lanthanide was then coordinated to the peptide via a diethylene triamine pentaacetic acid bifunctional agent. This method is a useful approach to the large‐scale synthesis of lanthanide3+‐coordinated, diethylene triamine pentaacetic acid labeled biopolymers. This research provides not only a simple and convenient method for the preparation of lanthanide‐based peptide ligand libraries but also possible lanthanide‐based high‐throughput screening of peptide receptors with a time‐resolved fluorescence assay system. Five biopolymers were synthesized and characterized with high‐resolution electrospray ionization in this study. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007