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Comparison of Edman Sequencing and Mass Spectrometry

1. Edman Sequencing

Edman sequencing is a method commonly used to determine the amino acid sequence of proteins and peptides. This process involves sequentially removing and identifying the N-terminal amino acids of a peptide or protein to achieve sequence determination. However, Edman degradation is a lengthy process, especially for large protein molecules, as each step of degradation takes a long time. Additionally, this method cannot determine modified amino acids, such as phosphorylation or acetylation. The advantage of Edman degradation is its minimal destructiveness to proteins or peptides, and its high accuracy in measurement.

2. Mass Spectrometry

Mass spectrometry is a method used to determine molecular mass, chemical structure, and amino acid sequences, with high sensitivity and accuracy. Compared with Edman sequencing, mass spectrometry can quickly and accurately determine the amino acid sequences of proteins and peptides, including modified amino acids. Additionally, mass spectrometry can analyze the primary, secondary, and tertiary structures of proteins. However, mass spectrometry requires complex equipment and specialized operational techniques, with certain requirements on sample quality and quantity.

3. Comparison

Both Edman sequencing and mass spectrometry have their unique advantages and applications. The advantage of Edman sequencing is its high accuracy and minimal destructiveness to proteins or peptides, but it is slower and cannot determine modified amino acids. On the other hand, the advantage of mass spectrometry is its fast sequencing speed and ability to determine modified amino acids and protein structures, but it requires complex equipment and specialized operational techniques. In practical applications, the choice of sequencing method is usually based on specific needs and conditions.

BiotechPack, A Biopharmaceutical Characterization and Multi-Omics Mass Spectrometry (MS) Services Provider

Related Services:

N-terminal sequencing of proteins based on Edman degradation

Protein N/C-terminal sequencing

Biopharmaceutical N/C-terminal sequencing

Sequence analysis based on mass spectrometry

Top-down protein sequencing

Protein interaction mass spectrometry analysis

Protein mass spectrometry identification

Peptide mass spectrometry identification

Pull-down target protein mass spectrometry identification

Protein interaction mass spectrometry analysis

Protein tandem mass spectrometry identification

Interacting protein mass spectrometry identification

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