Synergistic Interplay of Covalent and Non‐Covalent Interactions in Reactive Polymer Nanoassembly Facilitates Intracellular Delivery of Antibodies
Polymers
Surface Properties
Hydrolysis
Static Electricity
Proteins
Electrophoresis, Polyacrylamide Gel
beta-Galactosidase
01 natural sciences
Antibodies
Horseradish Peroxidase
0104 chemical sciences
DOI:
10.1002/anie.202010412
Publication Date:
2020-10-09T02:51:27Z
AUTHORS (4)
ABSTRACT
AbstractThe primary impediments in developing large antibodies as drugs against intracellular targets involve their low transfection efficiency and suitable reversible encapsulation strategies for intracellular delivery with retention of biological activity. To address this, we outline an electrostatics‐enhanced covalent self‐assembly strategy to generate polymer‐protein/antibody nanoassemblies. Through structure–activity studies, we down‐select the best performing self‐immolative pentafluorophenyl containing activated carbonate polymer for bioconjugation. With the help of an electrostatics‐aided covalent self‐assembly approach, we demonstrate efficient encapsulation of medium to large proteins (HRP, 44 kDa and β‐gal, 465 kDa) and antibodies (ca. 150 kDa). The designed polymeric nanoassemblies are shown to successfully traffic functional antibodies (anti‐NPC and anti‐pAkt) to cytosol to elicit their bioactivity towards binding intracellular protein epitopes and inducing apoptosis.
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