Paper
29 March 2005 Multiphoton, confocal, and lifetime microscopy for molecular imaging in cartilage
Sebastian Wachsmann-Hogiu, Deborah Krakow, Veneta T. Kirilova, Daniel H. Cohn, Cristina Bertolotto, Dora Acuna, Qiyin Fang, Nikola Krivorov, Daniel L. Farkas
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Abstract
It has recently been shown that mutations in Filamin A and B genes produce a large spectrum of skeletal disorders in developing fetuses. However, high-resolution optical microscopy in cartilage growth plate using fluorescent antibody assays, which should elucidate molecular aspects of these disorders, is extremely difficult due to the high level of autofluoresce in this tissue. We apply multiphoton, confocal, lifetime and spectral microscopy to (i) image and characterize autofluorophores in chondrocytes and subtract their contributions to obtain a corrected antibody-marker fluorescence signal, and (ii) measure the interaction between Filamin A and B proteins by detecting the fluorescence resonance energy transfer (FRET) between markers of the two proteins. Taking advantage of the different fluorescence spectra of the endogenous and exogenous markers, we can significantly reduce the autofluorescence background. Preliminary results of the FRET experiments suggest no interaction between Filamin A and B proteins. However, developing of new antibodies targeting the carboxy-terminal immunoglobulin-like domain may be necessary to confirm this result.
© (2005) COPYRIGHT Society of Photo-Optical Instrumentation Engineers (SPIE). Downloading of the abstract is permitted for personal use only.
Sebastian Wachsmann-Hogiu, Deborah Krakow, Veneta T. Kirilova, Daniel H. Cohn, Cristina Bertolotto, Dora Acuna, Qiyin Fang, Nikola Krivorov, and Daniel L. Farkas "Multiphoton, confocal, and lifetime microscopy for molecular imaging in cartilage", Proc. SPIE 5699, Imaging, Manipulation, and Analysis of Biomolecules and Cells: Fundamentals and Applications III, (29 March 2005); https://doi.org/10.1117/12.597670
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Cited by 2 scholarly publications.
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KEYWORDS
Confocal microscopy

Luminescence

Fluorescence resonance energy transfer

Cartilage

Proteins

Fluorescence lifetime imaging

Multiphoton microscopy

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