AI Article Synopsis

  • The synthesized matrix, α-cyano-5-phenyl-2,4-pentadienic acid (CPPA), shows improved effectiveness for protein analysis using MALDI-TOF MS, particularly in complex samples like food and bacteria.
  • Systematic UV absorption and LDI-MS experiments confirm CPPA's superior characteristics, such as enhanced protein signals and reduced variability in measurements.
  • Compared to traditional matrices, CPPA achieves better signal-to-noise ratios and consistency in protein profiling across various samples, making it a valuable addition to MALDI matrix options.

Article Abstract

The effectiveness of a synthesized matrix, α-cyano-5-phenyl-2,4-pentadienic acid (CPPA), for protein analysis by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) in complex samples such as foodstuff and bacterial extracts, is demonstrated. Ultraviolet (UV) absorption along with laser desorption/ionization mass spectrometry (LDI-MS) experiments were systematically conducted in positive ion mode under standard Nd:YLF laser excitation with the aim of characterizing the matrix in terms of wavelength absorption and proton affinity. Besides, the results for standard proteins revealed that CPPA significantly enhanced the protein signals, reduced the spot-to-spot variability and increased the spot homogeneity. The CPPA matrix was successful employed to investigate intact microorganisms, milk and seed extracts for protein profiling. Compared to conventional matrices such as sinapinic acid (SA), α-cyano-4-hydroxycinnamic acid (CHCA) and 4-chloro-α-cyanocinnamic acid (CClCA), CPPA exhibited better signal-to-noise (S/N) ratios and a uniform response for most examined proteins occurring in milk, hazelnut and in intact bacterial cells of . These findings not only provide a reactive proton transfer MALDI matrix with excellent reproducibility and sensitivity, but also contribute to extending the battery of useful matrices for intact protein analysis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7767571PMC
http://dx.doi.org/10.3390/molecules25246054DOI Listing

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