전자분무 이온화(ESI) 질량분석법

Electron-impact ionization causes severe molecular fragmentation of high molecular weight biomolecules like proteins and nucleic acids. Electrospray ionization is a soft ionization method that generates nonradical molecular ions, preserving the intact biomolecule structure. This allows mass spectrometry analysis of biomolecules without excessive decomposition.

The sample is mixed with a polar solvent and sprayed through a high-voltage capillary into a vacuum chamber. Electrical energy applied between the capillary and analysis chamber entrance moves charged droplets toward the chamber. Rapid solvent evaporation from the fine aerosol leaves behind charged gaseous sample molecules ready for mass detection.

The ionic liquid serves as the ionization source in the sample solution. It provides cations that associate with the analyte biomolecule during ionization. The type and mass of these cations directly affect the m/z values detected in the mass spectrum, determining peak positions.

An M+23 peak indicates that sodium ions from the ionic liquid have associated with the analyte molecule during ionization. The m/z value equals the sample's molecular mass plus 23, the atomic mass of sodium. Different cations produce different mass shifts, allowing identification of which ions are present.

The sample is mixed with polar solvents such as methanol, methanol-water, or acetonitrile, with or without added salts. These solvents facilitate the formation of charged droplets and enable efficient solvent evaporation. The choice of solvent and salt composition influences ionization efficiency and the types of cations available for association.

A biomolecule can associate with multiple cations during electrospray ionization, resulting in variably protonated or ionized species. Each association produces a distinct m/z value in the mass spectrum. The sum of the molecular mass and all associated ion masses determines the detected m/z, allowing analysis of chemical ionization mass spectrometry patterns.

The voltage difference applied between the capillary and the analysis chamber entrance creates an electric field that drives charged droplets toward the chamber. Higher voltage increases droplet acceleration and ionization efficiency. This electrical energy is fundamental to transferring ions from the liquid phase into the gaseous phase for mass analysis.