Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: EC:2.3.1.108 (
TAT
)
2,389
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
FcgammaRI requires both the intracellular domain of the
alpha-chain
and associated leukocyte Fc receptor (FcR) gamma-chains for its biological function. We recently found the C terminus of periplakin to selectively interact with the cytoplasmic domain of the FcgammaRI
alpha-chain
. It thereby enhances the capacity of FcgammaRI to bind, internalize, and present antigens on MHC class II. Here, we characterized the domains involved in FcgammaRI-periplakin interaction using truncated and alanine-substituted FcgammaRI mutants and randomly mutagenized periplakin. This allowed us to design
TAT
peptides that selectively interfered with endogenous FcgammaRI-periplakin interactions. The addition of these peptides to FcgammaRI-expressing cells modulated FcgammaRI ligand binding, as assessed by erythrocyte-antibody-rosetting. These data support a dominant-negative role of C-terminal periplakin for FcgammaRI biological activity and implicate periplakin as a novel regulator of FcgammaRI in immune cells.
...
PMID:Modulation of FcgammaRI (CD64) ligand binding by blocking peptides of periplakin. 1516 26
Here, we report that the MHC class I-related neonatal Fc receptor (
FcRn
) is expressed within azurophilic and specific granules of neutrophils and relocates to phagolysosomes on phagocytosis of IgG-opsonized bacteria. We found
FcRn
to enhance phagocytosis in a pH-dependent manner which was independent of IgG recycling. IgG-opsonized bacteria were inefficiently phagocytosed by neutrophils from beta2M knock-out or
FcRn
alpha-chain
knock-out mice, which both lack expression of
FcRn
. Similarly, low phagocytic activity was also observed with mutated IgG (H435A), which is incapable of binding to
FcRn
, while retaining normal binding to classical leukocyte Fcgamma receptors. Finally, a
TAT
peptide representing intracellular endocytosis and transport motifs within
FcRn
strongly inhibited IgG-mediated phagocytosis. These findings support a novel concept in which
FcRn
fulfills a major role in IgG-mediated phagocytosis.
...
PMID:FcRn: an IgG receptor on phagocytes with a novel role in phagocytosis. 1684 38