Gavuthami Murugesan

ORCID: 0000-0003-3422-4929
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About
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Research Areas
  • 14-3-3 protein interactions
  • Galectins and Cancer Biology
  • Glycosylation and Glycoproteins Research
  • Immunotherapy and Immune Responses
  • Monoclonal and Polyclonal Antibodies Research
  • Microbial Natural Products and Biosynthesis
  • Ubiquitin and proteasome pathways
  • Phagocytosis and Immune Regulation
  • Protein Kinase Regulation and GTPase Signaling
  • Melanoma and MAPK Pathways
  • Immune cells in cancer
  • Immune responses and vaccinations
  • Hepatitis C virus research
  • Immune Cell Function and Interaction
  • Proteoglycans and glycosaminoglycans research
  • Complement system in diseases
  • Animal Nutrition and Physiology
  • Cell Adhesion Molecules Research
  • Hepatitis B Virus Studies

Immunocore (United Kingdom)
2024

MRC Protein Phosphorylation and Ubiquitylation Unit
2014-2022

University of Dundee
2014-2022

Medical Research Council
2022

Capital Medical University
2021

Beijing Ditan Hospital
2021

Abstract Motivation: The 14-3-3 family of phosphoprotein-binding proteins regulates many cellular processes by docking onto pairs phosphorylated Ser and Thr residues in a constellation intracellular targets. Therefore, there is pressing need to develop new prediction methods that use an updated set 14-3-3-binding motifs for the identification targets prioritize downstream analysis >2000 potential interactors identified high-throughput experiments. Results: Here, comprehensive from...

10.1093/bioinformatics/btv133 article EN cc-by Bioinformatics 2015-03-03

The dimeric 14-3-3 proteins dock onto pairs of phosphorylated Ser and Thr residues on hundreds proteins, thereby regulate many events in mammalian cells. To facilitate global analyses these interactions, we developed a web resource named ANIA: ANnotation Integrated Analysis the interactome, which integrates multiple data sets 14-3-3-binding phosphoproteins. ANIA also pinpoints candidate phosphosites using predictor algorithms, assisted by our recent discovery that human 14-3-3-interactome is...

10.1093/database/bat085 article EN cc-by Database 2014-01-01

Abstract Siglec-15 is a conserved sialic acid-binding Ig-like lectin expressed on osteoclast progenitors, which plays an important role in development and function. It also by tumor-associated macrophages some tumors, where it thought to contribute the immunosuppressive microenvironment. was shown previously that engagement of macrophage-expressed with tumor cells expressing its ligand, sialyl Tn (sTn), triggered production TGF-β. In present study, we have further investigated interaction...

10.1093/glycob/cwaa048 article EN cc-by Glycobiology 2020-05-30

C-Type lectin receptor 5A (CLEC5A) is a spleen tyrosine kinase- (Syk-) coupled pattern recognition expressed on myeloid cells and involved in the innate immune response to viral bacterial infections. Activation of CLEC5A with pathogen-derived antigens leads secretion proinflammatory mediators such as TNF-α IL-6 that may provoke systemic cytokine storm, gene polymorphisms are associated severity DV infection. In addition, was mentioned context noninfectious disorders like chronic obstructive...

10.1155/2022/9926305 article EN cc-by Journal of Immunology Research 2022-02-25

: Siglec-1 is a macrophage lectin-like receptor that mediates sialic acid-dependent cellular interactions. Its upregulation on macrophages in autoimmune disease was shown previously to promote inflammation through suppressing the expansion of regulatory T cells (Tregs). Here we investigate molecular basis for binding Tregs using

10.12688/wellcomeopenres.16834.1 preprint EN cc-by Wellcome Open Research 2021-06-01

Macrophages (MΦ) are highly heterogenous and versatile innate immune cells involved in homeostatic responses. Activated MΦ can exist two extreme phenotypes: pro-inflammatory (M1) anti-inflammatory (M2) MΦ. These phenotypes be recapitulated vitro by using ligands of toll-like receptors (TLRs) cytokines such as IFNγ IL-4. In recent years, human induced pluripotent stem (iPSC)-derived have gained major attention, they functionally similar to monocyte-derived receptive genome editing. this...

10.3390/biomedicines10020239 article EN cc-by Biomedicines 2022-01-23

The protein kinases PAK4, PAK5 and PAK6 comprise a family of ohnologues. In multiple cancers including melanomas most frequently carries non-synonymous mutations; PAK4 have fewer; is often amplified. To help interpret these genomic data, initially we compared the cellular regulation sister their roles in melanoma cells. common with many ohnologue kinases, each two 14-3-3-binding phosphosites which phosphoSer99 conserved. localises to leading edge cells response phorbol ester-stimulated...

10.1042/bcj20220184 article EN cc-by Biochemical Journal 2022-08-15

Abstract The non-polymorphic HLA-E molecule offers opportunities for new universal immunotherapeutic approaches to chronic infectious diseases. Chronic Hepatitis B virus (HBV) infection is driven in part by T cell dysfunction due elevated levels of the HBV envelope (Env) protein hepatitis surface antigen (HBsAg). Here we report characterization three genotypic variants an HLA-E-binding HBsAg peptide, Env 371-379, identified through bioinformatic predictions and verified biochemical cellular...

10.1038/s41467-024-54378-9 article EN cc-by Nature Communications 2024-11-22

Two experiments were conducted to determine the effects of a phytogenic feed additive (PFA) on growth performance (exp. 1) and inflammation, oxidative stress, gut permeability, morphology 2) in nursery pigs. Dietary treatments were, basal diet [CON] + 0.015% PFA (Digestarom®, Biomin Holding GmbH). In exp. 1, pigs (n=315/trt, BW=5.79 ± 0.13 kg) allotted 21 pigs/pen for total 30 pens assigned within weight blocks dietary treatments. Pigs fed ad libitum pen BW disappearance measured d 19, 30,...

10.1093/jas/sky073.268 article EN Journal of Animal Science 2018-04-01

Abstract Siglec-1 is a macrophage lectin-like receptor that mediates sialic acid-dependent cellular interactions. It was shown previously to promote inflammation in autoimmune disease through suppressing the expansion of regulatory T cells (Tregs). We have investigated molecular basis for binding these using vitro -induced Tregs. strongly upregulated on activated cells, but lost under resting conditions. Glycosylation changes affect were studied by comparing and Tregs RNA-Seq, glycomics,...

10.1101/2020.07.29.226399 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2020-07-30
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