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Sarcomere Shortening of Pluripotent Stem Cell-Derived Cardiomyocytes using Fluorescent-Tagged Sarcomere Proteins.
Published on: March 3, 2021
Sarcomere length determination using front-face fluorescence polarization
1Centre INRA de Theix, UR370 QuaPA, F-63122 Saint-Genes-Champanelle, France.
Meat Science
|November 9, 2011
Summary
This study introduces a fluorescence anisotropy method to measure beef sarcomere length, aiding in detecting cold shortening and preventing meat toughness.
Area of Science:
- Muscle physiology
- Biophysics
- Food science
Background:
- Tryptophan is a key intrinsic fluorophore in muscle proteins.
- Proteins exhibit preferential alignments relative to muscle fiber direction.
- Muscle structure impacts meat quality characteristics like toughness.
Purpose of the Study:
- To estimate post-rigor sarcomere length in beef using tryptophan fluorescence.
- To develop an in-line detection method for cold shortening in meat.
- To correlate fluorescence anisotropy with meat structure and quality.
Main Methods:
- Utilized a theoretical model and front-face fluorescence polarization.
- Measured tryptophan fluorescence anisotropy.
- Assessed sarcomere length in beef samples (1.6–3.4 μm).
Main Results:
- Fluorescence anisotropy varied between normal, stretched, and cold-shortened beef samples.
- Cold shortening led to fiber misalignment, reducing anisotropy.
- The method successfully estimated sarcomere length.
Conclusions:
- Fluorescence anisotropy is a viable indicator of sarcomere length and cold shortening in beef.
- This technique can be applied for in-line quality control in the meat industry.
- Detecting cold shortening early can mitigate meat toughness.
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