TY - JOUR
T1 - Enzymatic Sialylation of Synthetic Multivalent Scaffolds
T2 - From 3′-Sialyllactose Glycomacromolecules to Novel Neoglycosides
AU - Konietzny, Patrick B.
AU - Peters, Hannelore
AU - Hofer, Marc L.
AU - Gerling-Driessen, Ulla I.M.
AU - de Vries, Robert P.
AU - Peters, Thomas
AU - Hartmann, Laura
N1 - Funding Information:
P.B.K. and H.P. contributed equally to this work. L.H. is corresponding author for synthetic chemistry and enzymatic reactions leading to the aglycon scaffolds, T.P. for enzymatic chemistry and in‐line NMR analysis. The authors thank the German Research Foundation for support through the research group “VIROCARB” (FOR 2327, P6/P7). The authors also thank Robert Creutznacher and Thorsten Biet for assistance with NMR experiments.
Publisher Copyright:
© 2022 The Authors. Macromolecular Bioscience published by Wiley-VCH GmbH.
PY - 2022/12
Y1 - 2022/12
N2 - Sialoglycans play a key role in many biological recognition processes and sialylated conjugates of various types have successfully been applied, e.g., as antivirals or in antitumor therapy. A key feature for high affinity binding of such conjugates is the multivalent presentation of sialoglycans which often possess synthetic challenges. Here, the combination is described of solid phase polymer synthesis and enzymatic sialylation yielding 3′-sialyllactose-presenting precision glycomacromolecules. CMP-Neu5Ac synthetase from Neisseria meningitidis (NmCSS) and sialyltransferase from Pasteurella multocida (PmST1) are combined in a one-pot reaction giving access to sequence-defined sialylated macromolecules. Surprisingly, when employing Tris(hydroxymethyl)aminomethane (Tris) as a buffer, formation of significant amounts of α-linked Tris-sialoside is observed as a side reaction. Further exploring and exploiting this unusual sialylation reaction, different neoglycosidic structures are synthesized showing that PmST1 can be used to derive both, sialylation on natural carbohydrates as well as on synthetic hydroxylated scaffolds.
AB - Sialoglycans play a key role in many biological recognition processes and sialylated conjugates of various types have successfully been applied, e.g., as antivirals or in antitumor therapy. A key feature for high affinity binding of such conjugates is the multivalent presentation of sialoglycans which often possess synthetic challenges. Here, the combination is described of solid phase polymer synthesis and enzymatic sialylation yielding 3′-sialyllactose-presenting precision glycomacromolecules. CMP-Neu5Ac synthetase from Neisseria meningitidis (NmCSS) and sialyltransferase from Pasteurella multocida (PmST1) are combined in a one-pot reaction giving access to sequence-defined sialylated macromolecules. Surprisingly, when employing Tris(hydroxymethyl)aminomethane (Tris) as a buffer, formation of significant amounts of α-linked Tris-sialoside is observed as a side reaction. Further exploring and exploiting this unusual sialylation reaction, different neoglycosidic structures are synthesized showing that PmST1 can be used to derive both, sialylation on natural carbohydrates as well as on synthetic hydroxylated scaffolds.
UR - http://www.scopus.com/inward/record.url?scp=85138725776&partnerID=8YFLogxK
U2 - 10.1002/mabi.202200358
DO - 10.1002/mabi.202200358
M3 - Journal articles
C2 - 36112275
AN - SCOPUS:85138725776
SN - 1616-5187
VL - 22
JO - Macromolecular Bioscience
JF - Macromolecular Bioscience
IS - 12
M1 - 2200358
ER -