Effect of polymer topology on non-covalent polymer–protein complexation: miktoarm versus linear mPEG-poly(glutamic acid) copolymers. Issue 14 (22nd March 2017)

• Record Type: Journal Article
• Authors: Nieto-Orellana, Alejandro; Di Antonio, Marco; Conte, Claudia; Falcone, Franco H.; Bosquillon, Cynthia; Childerhouse, Nick; Mantovani, Giuseppe; Stolnik, Snow
• Is Part Of: Polymer chemistry. Volume 8:Issue 14(2017)
• Page Start: 2210
• Page End: 2220
• Publication Date: 2017-03-22
• Subjects: Polymers -- Periodicals; Macromolecules -- Periodicals; Polymerization -- Periodicals; 547.705
• DOI: 10.1039/c7py00169j
• Languages: English
• ISSNs: 1759-9954

Abstract

Abstract : We report the design of mPEG-(poly(glutamic acid)) with different macromolecular topology – linear and miktoarm – for reversible non-covalent protein complexation. Abstract : Non-covalent polymer–protein conjugation is emerging as a potential route to improve pharmacokinetics and pharmacodynamics of protein therapeutics. In this study, a family of structurally related block copolymers of mPEG2k – poly(glutamic acid) with linear A-B (mPEG2k - lin -polyGA) and miktoarm A-B3 (mPEG2k - mik -(polyGA)3 ) structure was synthesised by N -carboxyanhydride (NCA) ring-opening polymerisation to assess the effect of macromolecular topology of the copolymers on polymer–protein complexation. The data illustrate that the synthesised copolymers are capable of complexing a model protein, lysozyme, at optimal pH conditions through non-covalent interactions, with complexation efficiencies depending on the copolymers composition and molecular architecture. In native gel electrophoresis experiments, linear mPEG2k - lin -GA10 copolymer, possessing a short polyanionic polyGA block, shows a low level of complexation, which does not change when the number of polyGA branches of the same size is increased, using a miktoarm mPEG2k - mik -(GA10 )3 copolymer. However, enhanced complexation is observed when the same number of ionisable GA units (30) are displayed on a linear macromolecular scaffold; mPEG2k - mik -(GA10 )3 vs. mPEG2k - lin -GA30 . Again complexation efficiency did not increase when the number of complexing polyGA branches were increased; mPEG2k - lin -GA30 vs. mPEG2k - mik -(GA30 )3 . Nanoparticle tracking analysis (NTA) showed that the copolymer–protein complexes possessed hydrodynamic diameters in the 50–200 nm range, suggesting a degree of control in the assembly process. Sequestration of lysozyme within polymer complexes resulted in a decrease in its apparent enzymatic activity, which was re-established on the complexes dissociation upon a treatment with competitive complexant. Intrinsic fluorescence and circular dichroism (CD) studies suggested structural conformation of the protein was not altered following complexation with mPEG2k -polyGA copolymers. Taken together, these results provide an initial structure–function relationship for protein-complexing mPEG2k -polyGA copolymers with variable macromolecular topology, opening the way for their future application in biological and biomedical studies.