Furyl-Alanine: A Novel Photo-Click Amino Acid

Furyl-Alanine: A Novel Photo-Click Amino Acid

Published on 31/03/2016

2-Furyl-alanine can be incorporated into peptides via SPPS or by using enzymatic approaches. UV-irradiation in the presence of oxygen and a photosensitizer converts furyl-alanine to an intermediate that selectively reacts with certain nucleophiles. This property can be employed for site-specific labeling of peptides and proteins.

Furyl-Alanine: A Novel Photo-Click Amino Acid

Labeling with different tags and reporter groups is a pivotal technique for the elucidation of peptide and protein function. A novel and innovative approach is the site-specific labeling using the unnatural amino acid 2-furyl-alanine. UV-irradiation in the presence of oxygen and a photosensitizer converts furyl-alanine to an unsaturated dicarbonyl compound. This intermediate selectively reacts with certain nucleophiles such as hydrazine derivatives of dyes or fluorescent labels. This reaction can be used for the site-specific labeling of peptides and proteins and can be carried out in aqueous solution.

2-Furyl-alanine can be incorporated into peptides either via SPPS or by using enzymatic approaches. Iris Biotech offers Fmoc-L-Ala(2-Furyl)-OH suitable for SPPS, as well as H-L-Ala(2-Furyl)-OH which can be incorporated into proteins using amber suppression methodology.

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