MALDI TOF 质谱

MALDI maintains structural integrity by embedding samples in a matrix that absorbs laser energy instead of directly ionizing the biomolecules. When the laser strikes the mixture, the matrix rapidly heats and desorbs, transferring energy to the biomolecules to ionize them gently. This preserves critical structural information that other ion sources remove from large, fragile molecules.

The matrix is an organic compound containing aromatic and conjugated double bonds that absorbs the majority of laser energy. When struck by the laser pulse, it rapidly heats and desorbs from the surface, transferring some energy to embedded biomolecules. The matrix must absorb laser energy, remain stable in vacuum, not react with target molecules, and be able to desorb effectively.

An electric field accelerates ions into a field-free drift tube, where their velocity correlates with mass-to-charge ratio—heavier particles travel slower. A detector measures each ion's flight time through the tube. Using the tube length, applied field strength, and flight time, the mass-to-charge ratio of each ion can be calculated and plotted as a mass spectrum.

The sandwich method involves streaking a saturated matrix solution onto a clean MALDI plate and drying it. Next, sample solution is added on top of the dried matrix spot. Finally, a second saturated matrix solution containing trifluoroacetic acid is applied on top, creating a three-layer sandwich. This method improves sample homogeneity and ionization efficiency.

MALDI is more robust because it is less sensitive to buffer components and contaminants present in samples. Electrospray ionization, by contrast, requires sample injection and is highly susceptible to contamination, making it less reliable for complex biological samples. MALDI's spotting procedure and matrix-based approach provide better tolerance for impurities.

MALDI can directly analyze living cells like macrophages after exposing them to signaling molecules called cytokines. Cells are added directly to the MALDI plate and analyzed. The resulting MALDI spectra serve as unique cellular fingerprints that vary depending on the cytokine used, allowing researchers to distinguish different cell states based on their molecular composition.

Complex biological samples like mammalian sebaceous secretions require purification before MALDI analysis. Thin layer chromatography is one technique that separates components based on polarity. Compounds are collected from the chromatography plate, purified, and transferred to a MALDI matrix. The resulting spectra verify the identity and purity of separated biomolecules, and unidentified compounds can be analyzed using tandem mass spectrometry principle instrumentation uses.