Hemoglobins from two individuals are compared by electrophoresis and by fingerprinting. Electrophoresis reveals no difference in migration, but fingerprinting shows an amino acid difference. How is this possible?

Key Concepts

Electrophoresis

Electrophoresis is a laboratory technique used to separate macromolecules, such as proteins or nucleic acids, based on their size and charge. In the context of hemoglobins, this method allows for the visualization of protein variants by their migration through a gel under an electric field. If two hemoglobins migrate identically, it suggests that they have similar charge and size, indicating no detectable differences in their overall structure.

Amino Acid Substitution

Amino acid substitution refers to a change in the protein sequence where one amino acid is replaced by another. This can occur due to mutations in the DNA that codes for the protein. While such substitutions may not affect the overall charge or size of the protein significantly enough to alter its migration in electrophoresis, they can still be detected through more sensitive methods like fingerprinting, which analyzes the specific sequence of amino acids.

Protein Fingerprinting

Protein fingerprinting is a technique used to identify proteins based on their unique patterns of amino acids or peptide fragments. This method can reveal subtle differences between proteins that may not be apparent through electrophoresis. Fingerprinting can detect variations in amino acid composition or sequence, allowing for the identification of distinct protein variants even when they exhibit similar physical properties in other analyses.