Assembly of High-Potency Photosensitizer–Antibody Conjugates through Application of Dendron Multiplier Technology
Author(s) -
Francesca Bryden,
Antoine Maruani,
João M. M. Rodrigues,
Miffy H. Y. Cheng,
Huguette Savoie,
Andrew Beeby,
Vijay Chudasama,
Ross W. Boyle
Publication year - 2017
Publication title -
bioconjugate chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.279
H-Index - 172
eISSN - 1520-4812
pISSN - 1043-1802
DOI - 10.1021/acs.bioconjchem.7b00678
Subject(s) - bioconjugation , chemistry , photosensitizer , conjugate , dendrimer , singlet oxygen , cytotoxicity , photodynamic therapy , combinatorial chemistry , biophysics , absorbance , porphyrin , in vitro , photochemistry , biochemistry , chromatography , organic chemistry , oxygen , mathematical analysis , mathematics , biology
Exploitation of photosensitizers as payloads for antibody-based anticancer therapeutics offers a novel alternative to the small pool of commonly utilized cytotoxins. However, existing bioconjugation methodologies are incompatible with the requirement of increased antibody loading without compromising antibody function, stability, or homogeneity. Herein, we describe the first application of dendritic multiplier groups to allow the loading of more than 4 porphyrins to a full IgG antibody in a site-specific and highly homogeneous manner. Photophysical evaluation of UV-visible absorbance and singlet oxygen quantum yields highlighted porphyrin-dendron 14 as the best candidate for bioconjugation; with subsequent bioconjugation producing a HER2-targeted therapeutic with average loading ratios of 15.4:1. In vitro evaluation of conjugate 18 demonstrated a nanomolar photocytotoxic effect in a target cell line, which overexpresses HER2, with no observed photocytotoxicity at the same concentration in a control cell line which expresses native HER2 levels, or in the absence of irradiation with visible light.
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