Squaric acid mediated chemoselective PEGylation of proteins: Reactivity of single-step-activated α-amino poly(ethylene glycol)s

Carsten Dingels, Frederik Wurm, Manfred Wagner, Harm Anton Klok, Holger Frey*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

20 Citations (Scopus)

Abstract

The covalent attachment of poly(ethylene glycol) (PEG) to therapeutically active proteins (PEGylation) has become an important method to deal with the pharmacological difficulties of these polypeptides, such as short body-residence times and immunogenicity. However, the derivatives of PEG used for PEGylation lack further functional groups that would allow the addition of targeting or labeling moieties. Squaric acid diethyl ester was used for the chemoselective single-step activation of poly(ethylene glycol)s into the respective ester amides. The resultant selective protein-reactive poly(ethylene glycol)s were investigated with respect to their selectivity towards amino acid residues in bovine serum albumin (as a model protein). The presented procedure relies on a robust two-step protocol and was found to be selective towards lysine residues; the activated polyethers are efficient and stoichiometric PEGylation agents with a remarkable hydrolytic stability over a period of several days. By adjusting the pD value of the conjugation mixture, the chemoselectivity of the activated PEGs towards the α- and ε-amino groups of lysine methyl ester was effectively changed. A square PEG: Squaric acid diethyl ester was established as a universal one-step activation agent for amino-terminated poly(ethylene glycol)s (PEGs) and was proven to be chemoselective towards the single amidation of α-amino-ω-hydroxy-PEG. Squaric acid ester amido PEGs exhibit a remarkable hydrolytic stability over a period of days in basic environments, which allows the stoichiometric PEGylation of proteins by formation of the squaric acid diamide with lysine groups (see figure).

Original languageEnglish
Pages (from-to)16828-16835
Number of pages8
JournalChemistry - A European Journal
Volume18
Issue number52
DOIs
Publication statusPublished - 21 Dec 2012
Externally publishedYes

Keywords

  • chemoselectivity
  • kinetics
  • PEGylation
  • proteins
  • squaric acid

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