Department of Biotechnology

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DEPARTMENT OF BIOTECHNOLOGY

Subject -- Instrumentation

Topic - Matrix Assisted laser Ionization(MALDI)

Submitted To -- Submitted BY --
Miss . Radha Kaushik Mam Deepanshu
INTRODUCTION
✓ MALDI is the abbreviation for “Matrix Assisted
Laser desorption/Ionization.”

✓ MALDI is appropriated to analyze biomolecules like


peptides, lipids, saccharides, or other organic
macromolecules.

✓ TOF stands for “Time of Flight”.

✓ This generates characteristic mass spectral


fingerprints which are compared with large library
of mass spectra.

✓ A versatile analytical technique to detect and


characterize mixtures of organic molecules.
Principle of MALDI

➢ Matrix absorbs the ultraviolet light (nitrogen laser light,


wavelength 337 nm) and converts it to heat energy.

➢ The analyte is embedded on the Target Plate.

➢ After a laser pulse, the irritated spot is rapidly heated and


becomes vibrationally excited.

➢ Matrix molecules energetically ablated from the surface of


the sample.

➢ During ablation, the analyte molecules are usually ionized


by being protonated or deprotonated with the nearby
matrix molecules.
TYPES OF MALDI VARIATION
➢ It may involve the absorption of light by the matrix .

➢ Transfer of this energy to the analyte –

• Which then ionizes into the gas phase as a result of


the relatively large amount of energy absorbed.

• To accelerating the resulting ions into a flight-tube


in the mass spectrometer they are subjected to a
high electric field.
❖ Used for the analysis of proteins and peptides.
Changes in structure can also be identified.

❖ Very Low amount of sample. Sample preparation is


easy and a spectrum is simple.

❖ Very fast separation method.

❖ Can be used to improve the diagnosis of infections


produced by viruses. It can also help discover
mutations and variants of these microorganisms and
detect antiviral resistance.

❖ Rapidly determine a mass pattern of proteins. It can


also identify specific protein markers and peptide
sequence variations among assessed species.

❖ Rapidly determine a mass pattern of proteins. It can


also identify specific protein markers and peptide
sequence variations among assessed species.

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