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Enzymatic Protein Immobilization on Amino-Functionalized Nanoparticles

The immobilization of proteins on nanoparticles has received much attention in recent years. Among different approaches, enzymatic protein immobilization shows unique advantages because of its site-specific connection. OaAEP1 is a recently engineered peptide ligase which can specifically recognize a...

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Detalles Bibliográficos
Autores principales: Ma, Qun, He, Boqiang, Tang, Guojin, Xie, Ran, Zheng, Peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9822503/
https://www.ncbi.nlm.nih.gov/pubmed/36615576
http://dx.doi.org/10.3390/molecules28010379
Descripción
Sumario:The immobilization of proteins on nanoparticles has received much attention in recent years. Among different approaches, enzymatic protein immobilization shows unique advantages because of its site-specific connection. OaAEP1 is a recently engineered peptide ligase which can specifically recognize an N-terminal GL residue (NH(2)–Gly–Leu) and a C-terminal NGL amino acid residue (Asn–Gly–Leu–COOH) and ligates them efficiently. Herein, we report OaAEP1-mediated protein immobilization on synthetic magnetic nanoparticles. Our work showed that OaAEP1 could mediate C-terminal site-specific protein immobilization on the amino-functionalized Fe(3)O(4) nanoparticles. Our work demonstrates a new method for site-specific protein immobilization on nanoparticles.