Paper
11 February 2011 A photophysical study of two fluorogen-activating proteins bound to their cognate fluorogens
Tiziano Gaiotto, Hau B. Nguyen, Jaemyeong Jung, Gnana S. Gnanakaran, Jurgen G. Schmidt, Geoffrey S. Waldo, Andrew M. Bradbury, Peter M. Goodwin
Author Affiliations +
Abstract
We are exploring the use of fluorogen-activating proteins (FAPs) as reporters for single-molecule imaging. FAPs are single-chain antibodies selected to specifically bind small chromophoric molecules termed fluorogens. Upon binding to its cognate FAP the fluorescence quantum yield of the fluorogen increases giving rise to a fluorescent complex. Based on the seminal work of Szent-Gyorgyi et al. (Nature Biotechnology, Volume 26, Number 2, pp 235-240, 2008) we have chosen to study two fluorogen-activating single-chain antibodies, HL1.0.1-TO1 and H6-MG, bound to their cognate fluorogens, thiazole orange and malachite green derivatives, respectively. Here we use fluorescence correlation spectroscopy to study the photophysics of these fluorescent complexes.
© (2011) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Tiziano Gaiotto, Hau B. Nguyen, Jaemyeong Jung, Gnana S. Gnanakaran, Jurgen G. Schmidt, Geoffrey S. Waldo, Andrew M. Bradbury, and Peter M. Goodwin "A photophysical study of two fluorogen-activating proteins bound to their cognate fluorogens", Proc. SPIE 7905, Single Molecule Spectroscopy and Imaging IV, 79050O (11 February 2011); https://doi.org/10.1117/12.875418
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KEYWORDS
Proteins

Fluorescence correlation spectroscopy

Luminescence

Diffusion

Imaging spectroscopy

Molecules

Avalanche photodetectors

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