4.7 Article

Comparison of different digestion methods for proteomic analysis of isolated cells and FFPE tissue samples

期刊

TALANTA
卷 233, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.talanta.2021.122568

关键词

Proteomics; FASP; Pressure-cycling digestion; In-solution digestion; Cellular subpopulations; FFPE tissue Proteomics

资金

  1. project International Centre for Cancer Vaccine Science
  2. European Union under the European Regional Development Fund
  3. European Regional Development Fund -Project ENOCH [CZ.02.1.01/0.0/0.0/16_019/0000868]
  4. Ministry of Health Development of Research Organization, MH CZ -DRO (MMCI) [00209 805]

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This study compared several protocols for proteomic sample preparation and found that the ISD method is highly efficient in protein and peptide identification from the whole proteome, while the FASP method is effective in identifying membrane proteins. Pressure-assisted digestion methods are gaining popularity due to their shorter digestion time, although they generally provide lower numbers of protein/peptide identifications.
Proteomics of human tissues and isolated cellular subpopulations create new opportunities for therapy and monitoring of a patients' treatment in the clinic. Important considerations in such analysis include recovery of adequate amounts of protein for analysis and reproducibility in sample collection. In this study we compared several protocols for proteomic sample preparation: i) filter-aided sample preparation (FASP), ii) in-solution digestion (ISD) and iii) a pressure-assisted digestion (PCT) method. PCT method is known for already a decade [1], however it is not widely used in proteomic research. We assessed protocols for proteome profiling of isolated immune cell subsets and formalin-fixed paraffin embedded (FFPE) tissue samples. Our results show that the ISD method has very good efficiency of protein and peptide identification from the whole proteome, while the FASP method is particularly effective in identification of membrane proteins. Pressure-assisted digestion methods generally provide lower numbers of protein/peptide identifications, but have gained in popularity due to their shorter digestion time making them considerably faster than for ISD or FASP. Furthermore, PCT does not result in substantial sample loss when applied to samples of 50 000 cells. Analysis of FFPE tissues shows comparable results. ISD method similarly yields the highest number of identifications. Furthermore, proteins isolated from FFPE samples show a significant reduction of cleavages at lysine sites due to chemical modifications with formaldehyde-such as methylation (+14 Da) being among the most common. The data we present will be helpful for making decisions about the robust preparation of clinical samples for biomarker discovery and studies on pathomechanisms of various diseases.

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