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An economical and preparative orthogonal solid phase synthesis of fluorescein and rhodamine derivatized peptides: FRET substrates for the Staphylococcus aureus sortase SrtA transpeptidase reaction Export

by: Ryan G. Kruger, Patrick Dostal, Dewey G. Mccafferty
Chem. Commun., No. 18. (2002), pp. 2092-2093.

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chemistry chemistry-conjugation fluorescence peptides

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An economical and preparative-scale orthogonal solid-phase method of incorporating carboxyrhodamine and carboxyfluorescein fluorescence resonance energy transfer (FRET) probes site-specifically into synthetic peptide substrates for the S. aureus Sortase transpeptidase SrtA has been developed.


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