Engineered Protein Copolymers for Heparin Neutralization and Detection
Loading...
Access rights
openAccess
publishedVersion
URL
Journal Title
Journal ISSN
Volume Title
A1 Alkuperäisartikkeli tieteellisessä aikakauslehdessä
This publication is imported from Aalto University research portal.
View publication in the Research portal (opens in new window)
View/Open full text file from the Research portal (opens in new window)
View publication in the Research portal (opens in new window)
View/Open full text file from the Research portal (opens in new window)
Date
Department
Major/Subject
Mcode
Degree programme
Language
en
Pages
8
Series
Biomacromolecules, Volume 24, issue 2, pp. 1014-1021
Abstract
Heparin is a widely applied anticoagulant agent. However, in clinical practice, it is of vital importance to reverse its anticoagulant effect to restore the blood-clotting cascade and circumvent side effects. Inspired by protein cages that can encapsulate and protect their cargo from surroundings, we utilize three designed protein copolymers to sequester heparin into inert nanoparticles. In our design, a silk-like sequence provides cooperativity between proteins, generating a multivalency effect that enhances the heparin-binding ability. Protein copolymers complex heparin into well-defined nanoparticles with diameters below 200 nm. We also develop a competitive fluorescent switch-on assay for heparin detection, with a detection limit of 0.01 IU mL–1 in plasma that is significantly below the therapeutic range (0.2–8 IU mL–1). Moreover, moderate cytocompatibility is demonstrated by in vitro cell studies. Therefore, such engineered protein copolymers present a promising alternative for neutralizing and sensing heparin, but further optimization is required for in vivo applications.Description
Keywords
Other note
Citation
Liu, Q, Shaukat, A, Meng, Z, Nummelin, S, Tammelin, T, Kontturi, E, De Vries, R & Kostiainen, M 2023, 'Engineered Protein Copolymers for Heparin Neutralization and Detection', Biomacromolecules, vol. 24, no. 2, pp. 1014-1021. https://doi.org/10.1021/acs.biomac.2c01464