“…For α-chymotrypsin, the widely applied method for polymer conjugation with epoxy-functional polymers involves amination of the epoxy group with a diamine followed by coupling the resulting amine-functionalized polymer to the enzyme by glutaraldehyde [114,115]. Although poly(N-isopropylacrylamide) bioconjugates have been investigated in numerous cases, its relatively large extent of hysteresis due to hydrogen bonding between PNIPAAm chains [46,47] and even full activity loss of the conjugated enzyme [122] may limit its application possibilities. In contrast, the lack of hydrogen bonding between PDEAAm chains may provide unique advantages for bioconjugations with functional PDEAAm.…”
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“…For α-chymotrypsin, the widely applied method for polymer conjugation with epoxy-functional polymers involves amination of the epoxy group with a diamine followed by coupling the resulting amine-functionalized polymer to the enzyme by glutaraldehyde [114,115]. Although poly(N-isopropylacrylamide) bioconjugates have been investigated in numerous cases, its relatively large extent of hysteresis due to hydrogen bonding between PNIPAAm chains [46,47] and even full activity loss of the conjugated enzyme [122] may limit its application possibilities. In contrast, the lack of hydrogen bonding between PDEAAm chains may provide unique advantages for bioconjugations with functional PDEAAm.…”
Commons Attribution (CC BY) license, which allows users to download, copy and build upon published articles, as long as the author and publisher are properly credited, which ensures maximum dissemination and a wider impact of our publications.
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