Category Archives: CH3 Blog

Collection of news and reviews from CH3 with protein methylation in the cellular development of neuronal model systems

SMAD6 Methylation Reduces Periodontal Inflammation

Continuing last week’s post about protein methylation in cellular inflammatory responses, we would like to call attention to the recent publication by Zhang et al. The authors explain how PRMT1-SMAD6 signaling may represent a new target for reducing the immune response in periodontitis (see Figure): Lipopolysacchride (LPS) from oral pathogens activate toll-like receptors (TLR) which […]

Protein Methylation in Cellular Inflammatory Responses

We are thinking a lot lately about the role of protein methylation in cellular inflammatory responses. The connection between the two is not a new idea. There are numerous clues in the primary scientific literature that functionally link protein methylation with inflammation. See for example the recent review by Webb and Guerau-de-Arellano There will be […]

New Analysis of Protein Arginine Methylation in Colorectal Cancer

This week’s blog post highlights a recent study by Lim et al. This proteome-wide analysis of protein arginine methylation in colorectal cancer based on human surgical specimens is another example of the developments occurring in our field with real impact on disease diagnosis. For histological detection of the methylation status of colon cancer, we recommend […]

Important Translational Research News About Fragile X Mental Retardation and Cancer

CH3 BioSystems is excited about an important review article recently published by Majumder et al. that helps to explain the role of methylarginine modification in the functional regulation the fragile X family of proteins with implications for neurodevelopment and cancer. In conjunction with phospho-serine modifications of these methyl-proteins, the molecular mechanisms involved are likely to […]

New Discoveries in Protein Methylation

A ground-breaking report from scientists at Glaxo and Epizyme has now revealed that the PRMT1 inhibitor, GSK3368715, exhibits potent anti-tumor activity. Extensive chemical and cellular studies support the usefulness of the new chemical compound as a First-In-Class therapeutic agent. Also described in the report are experiments that implicate the endogenous metabolic inhibitor, methyl-thioadenosine (MTA), in […]

Research Review Series (2 of 3)

THE INTERSECTION OF CANCER AND PROTEIN METHYLATION   William Pratt, CH3 Biosystems Lab Intern Introduction   Protein arginine methyltransferases (PRMTs) are transcriptional coactivators, a type of coregulator that affects a transcription factor to increase the rate of transcription of a gene by recruiting general transcription machinery to the promoter region. The aberrant expression of PRMTs […]