タンデム質量分析法を使用したペプチドの同定

Tandem mass spectrometry, or MS/MS, uses two mass analyzers in series separated by a collision cell, unlike single mass spectrometry. The first analyzer selects a specific peptide ion, which then fragments in the collision cell. The second analyzer separates the resulting product ions to build a fragmentation pattern, enabling amino acid sequence identification from complex mixtures.

The collision cell is positioned between the two mass analyzers and contains gas molecules that collide with the selected peptide ion. These collisions primarily break peptide bonds, generating smaller fragment ions. The resulting product ions then enter the second mass analyzer, where their mass-to-charge ratios are measured to determine the peptide's amino acid sequence.

Combining MS/MS with liquid chromatography enables continuous peptide analysis from complex biological samples. Liquid chromatography separates peptides based on physical size and chemical properties before they enter the mass spectrometer, reducing sample complexity and improving the accuracy of peptide identification and sequencing.

A product-ion spectrum displays the mass-to-charge ratios of fragment ions generated when a peptide breaks apart in the collision cell. This spectrum reveals the peptide's amino acid sequence by showing the pattern of fragments produced. Analysis software compares the obtained spectrum with protein databases to identify unknown peptides from overlapping fragments.

Tandem mass spectrometry can characterize lipids, identify post-translational protein modifications, and detect low levels of disease-specific biomarkers in biological samples. In newborn screening, MS/MS analyzes dried blood-spot samples to detect inborn metabolic disorders like phenylketonuria and sickle cell disease, enabling early intervention and improved health outcomes.

Different analyzer combinations create hybrid MS/MS instruments that increase sensitivity and resolution. For example, quadrupole time-of-flight (QTOF) combines quadrupole and time-of-flight analyzers, while triple quadrupole instruments use two quadrupole mass analyzers separated by a collision cell. These configurations enhance the detection and characterization of peptides and other biomolecules.

Bioinformatics tools and protein database search algorithms compare the obtained MS/MS spectrum with databases of known peptide sequences. Since each protein produces a unique spectral pattern, the software matches overlapping fragments from unknown samples against known sequences, allowing researchers to identify proteins and peptides from complex biological mixtures.