A1 Refereed original research article in a scientific journal

Derivatization of phosphopeptides with mercapto- and amino-functionalized conjugate groups by phosphate elimination and subsequent Michael addition




AuthorsMattila K, Siltainsuu J, Balaspiri L, Ora M, Lonnberg H

PublisherROYAL SOC CHEMISTRY

Publication year2005

Journal:Organic and Biomolecular Chemistry

Journal name in sourceORGANIC & BIOMOLECULAR CHEMISTRY

Journal acronymORG BIOMOL CHEM

Volume3

Issue16

First page 3039

Last page3044

Number of pages6

ISSN1477-0520

DOIhttps://doi.org/10.1039/b505573c


Abstract
Kinetics of the beta-elimination of the phosphate group from H-Tyr-Ser(PO3H2)-Phe-OH and H-Tyr-Thr(PO3H2)-Phe-OH and subsequent addition of thiols and amines to the dehydroalaninyl and beta-methyldehydroalaninyl residues formed, were followed by RP HPLC under alkaline conditions in the absence and presence of Ba2+ ions. By this reaction sequence, the phosphoserinyl peptide was conjugated with mono-N-(2-mercaptoethyl) amide of 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid ( 4), a mercapto-functionalized pentapeptide, H-His-Gly-Gly-His-Gly-NH(CH2)(4)SH, and an amino-functionalized fluorescent dye, 5-dimethylaminonaphthalene-1-[N-(5-aminopentyl)] sulfonamide (dansyl cadaverine). The beta-methyldehydroalanine residue was, in turn, observed to be a poor Michael acceptor.


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