AnaSpec Introduces Fluorescent GO<sup>TM</sup> Peptides

17 Jun 2009
Emily Marquez-Vega
Publishing / Media

Fluorescent peptides, peptides with a reporter fluorescent dye, are valuable probes used in visualizing intracellular processes and molecular interactions at the level of single cells.(1) The fluorescent dye can be attached to the amino (N) or carboxy (C)-terminus, or in the case of FRET (Fluorescence or Förster resonance energy transfer) peptides, the two dyes (donor and acceptor) can be at the amino and carboxy termini or in the internal peptide sequence.

Leveraging its dual expertise in peptides and fluorescent dyes, AnaSpec is pleased to offer a broad selection of fluorescently labeled peptides labeled with our proprietary HiLyte Fluor™ dyes, as well as classic dyes (FAM, FITC, TAMRA).

For use as enzyme activity detection probes
Peptide substrates used in detection of enzyme activity can contain either a single dye or in the case of FRET, two dyes. In the intact fluorescent substrates, there is low fluorescence prior to enzyme hydrolysis. Upon recognition of the substrate by a specific enzyme and subsequent cleavage, the quenched fluorescence is recovered. Increase in fluorescence is correlated to enzyme activity.(2-3) AnaSpec’s single dye-labeled fluorescent peptide selection include substrates for kinases, caspases, cathepsins, HDAC (histone deacetylase), calpain, kallikrein, and others. Our FRET peptides, generally consisting of a dye (donor) and a non-fluorescent quencher (acceptor), include substrates for MMPs, Aggrecanase-1, HCV, HIV, cathepsins, renin, ACE2, α and β-secretases and others.

For use as targeting probes
Fluorescent peptides have been used in in vivo or in vitro studies for visualizing cellular processes and molecular interactions.(1) In in vivo imaging, three-dimensional fluorescence images of the internal structures, especially of small animals, are produced. This technique requires the use of near infrared red (NIR) dyes since at higher wavelength, tissues do not absorb or scatter photons as strongly as when lower wavelength dyes are used.(2-3)

References:
(1). Pap, EHW. et al. Exp. Cell Res. 265, 288 (2001).
(2). Lakowicz, Joseph. Principles of Fluorescence Spectroscopy. New York: Springer, 2006.
(3). Tung, C-H. Peptide Sci. 76, 391 (2004).

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