
Protein propionylation is a newly discovered reversible post-translational modification. This process involves the covalent attachment of a propionyl group (from donors like propionyl-CoA) to lysine residues on substrate proteins, catalyzed by acyltransferases. As a newly identified modification type, propionylation plays important regulatory roles in both eukaryotes and prokaryotes. Research shows that this modification is widely involved in global metabolic regulatory networks and metabolic enzyme activity regulation in bacteria, playing key roles in cellular stress responses, epigenetic regulation, and metabolism-related physiological processes.
Propionylation participates in regulating core cellular life activities by influencing various mechanisms including protein stability, protein subcellular localization, metabolic enzyme activity, transcriptional activity of transcription factors, protein-protein interactions, and protein-DNA interactions. With the rapid development of proteomics and mass spectrometry technologies, propionylation modification, as an important member of the histone lysine acylation modification family, is increasingly demonstrating its research value.
We provide comprehensive and professional propionylation proteomics analysis services, including:
Our propionylation proteomics service platform offers the following core strengths:
Protein extraction and quantification are performed using standardized protocols based on the sample type.
Protein samples are digested using specific proteases, with multi-enzyme strategies employed to increase coverage.
Propionylated peptides from the digest are enriched using propionylation-specific antibodies via immunoaffinity purification.
Enriched peptides are separated by high-performance liquid chromatography and analyzed by high-resolution mass spectrometry.
Raw MS data is acquired and processed using professional software for database searching and statistical analysis.
A comprehensive bioinformatics analysis is conducted on the identified propionylated proteins and sites to uncover their biological significance.
A detailed technical report is provided, including the experimental procedure, MS parameters, identification results, and bioinformatics analysis content.
To ensure accurate experimental results, please refer to the following sample requirements:
| Sample Type | Minimum Amount Required |
| Plant Leaves | Wet weight ≥ 0.8 g |
| Plant Roots, Stems, Xylem, Phloem, etc. | Wet weight ≥ 10 g |
| Cell Samples | Cell count equivalent to wet weight ≥ 8×10⁷ |
| Tissue Samples (Human, Animal, Microbial) | Wet weight ≥ 300 mg |
| Body Fluid Samples | Serum/Plasma volume ≥ 1 ml, CSF ≥ 1 ml, Urine ≥ 50 ml |
All samples must be stored in liquid nitrogen or at -80°C and shipped with sufficient dry ice to avoid repeated freeze-thaw cycles.
Propionylation proteomics provides a powerful tool for deciphering the sophisticated regulatory mechanisms in living organisms. We look forward to supporting your research with professional and reliable technical services, helping you uncover new insights into protein modifications.