Bioorthogonal oxime ligation mediated in vivo cancer targeting

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Bioorthogonal oxime ligation mediated in vivo cancer targeting

Department of Materials Science and Urbana–Champaign, 1304 West Green S [email protected]; Fax: +1-217-333-2736 Department of Pharmaceutical Science, Guangzhou, Guangdong, 510006, China Department of Bioengineering, University o IL 61801, USA † Electronic supplementary informatio characterization of compounds and nan cell labelling with liposomes, PET/CT im 10.1039/c5sc00063g ‡ Contributed ...

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Bioorthogonal oxime ligation mediated in vivo cancer targeting† †Electronic supplementary information (ESI) available: Synthesis and characterization of compounds and nanoparticles, in vitro and in vivo tumor cell labelling with liposomes, PET/CT imaging and biodistribution. See DOI: 10.1039/c5sc00063g Click here for additional data file.

Current cancer targeting relying on specific biological interaction between cell surface antigen and respective antibody or its analogue has proven to be effective in the treatment of different cancers; however, this strategy has its own limitations, such as heterogeneity of cancer cells and immunogenicity of the biomacromolecule binding ligands. Bioorthogonal chemical conjugation has emerged a...

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Diverse organo-peptide macrocycles via a fast and catalyst-free oxime/intein-mediated dual ligation.

Macrocyclic Organo-Peptide Hybrids (MOrPHs) can be prepared from genetically encoded polypeptides via a chemoselective and catalyst-free reaction between a trifunctional oxyamino/amino-thiol synthetic precursor and an intein-fusion protein incorporating a bioorthogonal keto group.

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ژورنال

عنوان ژورنال: Chemical Science

سال: 2015

ISSN: 2041-6520,2041-6539

DOI: 10.1039/c5sc00063g