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Targeted Quantification of Protein Phosphorylation and Its Contributions towards Mathematical Modeling of Signaling Pathways

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MOLECULES
卷 28, 期 3, 页码 -

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MDPI
DOI: 10.3390/molecules28031143

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targeted phosphoproteomics; LC-SRM; quantification; phosphorylation; signaling; mathematical modeling; cancer

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Post-translational modifications (PTMs), especially phosphorylation, play a crucial role in regulating protein function. Traditional immunological assays often lack sensitivity and specificity for quantitative measurements of protein phosphorylation. Recent advances in Mass Spectrometry (MS)-based targeted proteomics, such as selected reaction monitoring (SRM) and parallel reaction monitoring (PRM), have greatly improved the accuracy and reliability of phosphoprotein quantification. This quantitative data can be used to build mathematical models of phospho-signaling pathways, providing valuable insights for better diagnosis and treatment of diseases.
Post-translational modifications (PTMs) are key regulatory mechanisms that can control protein function. Of these, phosphorylation is the most common and widely studied. Because of its importance in regulating cell signaling, precise and accurate measurements of protein phosphorylation across wide dynamic ranges are crucial to understanding how signaling pathways function. Although immunological assays are commonly used to detect phosphoproteins, their lack of sensitivity, specificity, and selectivity often make them unreliable for quantitative measurements of complex biological samples. Recent advances in Mass Spectrometry (MS)-based targeted proteomics have made it a more useful approach than immunoassays for studying the dynamics of protein phosphorylation. Selected reaction monitoring (SRM)-also known as multiple reaction monitoring (MRM)-and parallel reaction monitoring (PRM) can quantify relative and absolute abundances of protein phosphorylation in multiplexed fashions targeting specific pathways. In addition, the refinement of these tools by enrichment and fractionation strategies has improved measurement of phosphorylation of low-abundance proteins. The quantitative data generated are particularly useful for building and parameterizing mathematical models of complex phospho-signaling pathways. Potentially, these models can provide a framework for linking analytical measurements of clinical samples to better diagnosis and treatment of disease.

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