Spontaneous and site-specific immobilization of PNGase F via spy chemistry.

ABSTRACT: Protein N-glycosylation plays a critical role in a wide range of biological processes, and aberrant N-glycosylation is frequently associated with various pathological states. For global N-glycosylation analysis, N-glycans are typically released from glycoproteins mediated by endoglycosidases, primarily peptide N-glycosidase F (PNGase F). However, conventional N-glycan release by in-solution PNGase F is time-consuming and nonreusable. Although some immobilization methods can save time and reduce the enzyme dosage, including affinity interaction and covalent binding, the immobilized PNGase F by these traditional methods may compromises the immobilized enzyme's stability and biofunction. Therefore, a new approach is urgently needed to firmly and stead

SUBMITTER: Zhang L 

PROVIDER: S-EPMC10523939 | biostudies-literature | 2023 Sep

REPOSITORIES: biostudies-literature