4.7 Article

Luminescence detection of peptide:N-glycanase activity using engineered split inteins

Journal

CHEMICAL COMMUNICATIONS
Volume 58, Issue 95, Pages 13282-13285

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2cc04865e

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Funding

  1. AMED-CREST [JP22gm1410003]

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A split intein-based method has been developed to detect PNGase activity in live cells. The method utilizes protein trans-splicing between N-intein peptides and C-intein to generate an active luciferase, resulting from the cleavage of the N,N '-diacetylchitobiose linkage by PNGase.
A split intein-based method has been developed to detect peptide:N-glycanase (PNGase) activity in live cells. PNGase cleaves the linkage between N,N '-diacetylchitobiose and the Asn side-chain of N-intein peptides and the products react rapidly with C-intein by protein trans-splicing to generate an active luciferase.

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