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Using BLAST to Analyze Proteins Part 2: Comparing Fluorescent Proteins

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Presentation on theme: "Using BLAST to Analyze Proteins Part 2: Comparing Fluorescent Proteins"— Presentation transcript:

1 Using BLAST to Analyze Proteins Part 2: Comparing Fluorescent Proteins
2013 Workshop C: Cloning DNA to Make Proteins Dina N Kovarik, MS, PhD NWABR

2 Fluorescent Proteins are Valuable Tools
Locate proteins in the cell Track the migration of cells Reporter of expression Sister centromeres (green) mark the attachment of microtubules (red) to sister chromatids (blue). Left: Normal. Right: Drug-treated. Mice expressing GFP under UV light (left & right), compared to normal mouse (center). Source: Wikipedia. Source:

3 Bioluminescence of the crystal jellyfish, Aequorea victoria
238 amino acid proteins. GFP ribbon diagram. From PDB 1EMA. Source: Wikipedia Source:

4 Rainbow of Fluorescent Proteins
“Drawn” with bacteria expressing 8 different fluorescent proteins Diversity of Mutations  Diversity of Colors “mFruits” mBlueberry (Blue Fluorescent Protein, or BFP) mLemon (Yellow Fluorescent Protein, or YFP) mGrape1 (Cyan Fluorescent Protein, or CFP) Many others, all with similarly ‘fruity’ names… Source: Wikipedia.

5 Diversity and Key Mutations

6 Research Questions The cloning and protein purification experiments you have been conducting in the laboratory involve mTomato (related to mCherry), also called red fluorescent protein (RFP). Is red fluorescent protein (RFP) related to its famous cousin, GFP, or is from a different source entirely? What other fluorescent proteins, if any, are closely related to RFP?

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