Title : Mannose-functionalized antigen nanoparticles for targeted dendritic cells, accelerated endosomal escape and enhanced MHC-I antigen presentation.

Pub. Date : 2021 Jan

PMID : 33010719






4 Functional Relationships(s)
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1 Model antigen ovalbumin (OVA) was directly conjugated with mannose to obtain DCs targeting antigen, which was then complexed with polyethylenimine (PEI) through electrostatic interaction to form mannose-functionalized antigen nanoparticles (MAN-OVA/PEI NPs). Polyethyleneimine serine (or cysteine) peptidase inhibitor, clade B, member 1, pseudogene Mus musculus
2 Model antigen ovalbumin (OVA) was directly conjugated with mannose to obtain DCs targeting antigen, which was then complexed with polyethylenimine (PEI) through electrostatic interaction to form mannose-functionalized antigen nanoparticles (MAN-OVA/PEI NPs). Polyethyleneimine serine (or cysteine) peptidase inhibitor, clade B, member 1, pseudogene Mus musculus
3 Model antigen ovalbumin (OVA) was directly conjugated with mannose to obtain DCs targeting antigen, which was then complexed with polyethylenimine (PEI) through electrostatic interaction to form mannose-functionalized antigen nanoparticles (MAN-OVA/PEI NPs). Polyethyleneimine serine (or cysteine) peptidase inhibitor, clade B, member 1, pseudogene Mus musculus
4 Model antigen ovalbumin (OVA) was directly conjugated with mannose to obtain DCs targeting antigen, which was then complexed with polyethylenimine (PEI) through electrostatic interaction to form mannose-functionalized antigen nanoparticles (MAN-OVA/PEI NPs). Polyethyleneimine serine (or cysteine) peptidase inhibitor, clade B, member 1, pseudogene Mus musculus