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Home >> Biotechnology and Genomics >> Mass Spectrometry - An Essential Tool for Genome and Proteome Analysis >>Mass Spectrometers and Mass Spectral Analysis

Mass Spectrometers and Mass Spectral Analysis
Essentially, a mass spectrometer measures mass-to-charge (m/z) ratios of analytes such as nucleic acids, oligonucleotides, proteins, peptides or peptide fragments. It has three components, ionization source, the m/z analyzer and the detector.

Simplified schematic of a Mass Spectrometer

Simplified Schematic of a mass Spectrometer(MS)


 

Following three principles are applied for separation of molecules that differ in mass: (i) separation of ions on the basis of time of flight (TOF MS); (ii) separation of ions by quadrupole electric field generated by metal rods (quadrupole MS) and (iii) separation of ions by selective ejection of ions from a three-dimensional trapping field (ion trap or Fourier transform ion cyclotron MAS). Any of the ionization methods described above, including MALCDI, Es or FAB can be coupled with any of the above three methods of ion separation. However, since MALDI produces short bursts of ions in vacuum, it is coupled with TOF MS, while Electrospray (ES), producing continuous beam of ions in atmosphere is coupled with quadrupole and ion trapping MS.

In 1890, J.J Thomson introduced the first mass spectrometer, which employed fixed magnetic and electric fields (described as electric sector and magnetic sector) to separate ions of different mass and energy. He recognized that charged particles that differ in momentum behave differently in an electromagnetic field and used this property for separation of ions with different masses. Using this instrument, he was able to prove that the noble gas Ne (Neon) was composed of two different isotopes of mass 20 Da and 22 Da. These so called ‘sector instruments’ are not very sensitive in comparison with recent mass spectrometers and are now more or less of historical importance. Some advantages although not unique, are their relatively high mass range, sensitiveity and resolving power, and their compatibility with wide range of ionization techniques. The disadvantages are their size and cost compared to most other mass spectrometers developed later.

 

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