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Syntheses and Functions of Glycosaminoglycan Mimicking Polymers

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Coupling and Decoupling of Diverse Molecular Units in Glycosciences
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Abstract

Glycosaminoglycans (GAGs) are important polysaccharides in the living system. Though total syntheses of GAGs oligosaccharides have been reported, it is still difficult to obtain GAGs. In this investigation, GAGs mimetics were prepared by polymerization of vinyl sugars instead of total synthesis. Glycopolymers are polymers with pendant saccharides, and exhibit a strong molecular recognition due to the multivalency. GAGs mimicking glycopolymers were prepared by polymerizing acrylamide derivatives carrying sulfated N-acetyl glucosamine (GlcNAc). The polymer interactions with proteins were investigated. The glycopolymer libraries were prepared with varying molecular weight, sugar structure, and sugar ratios. The GAG glycopolymers with biodegradable backbone, dendrimer, and arrays were also prepared. The inhibitory activity of Alzheimer amyloid beta peptides by the glycopolymers was investigated in detail. The glycopolymer with sulfated GlcNAc inhibited the aggregation of amyloid beta (Aβ) and the multivalency of sulfated GlcNAc was the key of the interaction. The activity depends on the chemical structure of glycopolymers. Also, the sulfated saccharide function was correlated to the functions of native GAGs.

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References

  1. Taylor ME, Drickamaer K (2002) Introduction to glycobiology. Oxford Press, London

    Google Scholar 

  2. Rudd TR, Skidomore MA, Guerrini M, Hricovini M, Powell AK, Siligardi G, Yates EA (2010) The conformation and structure of GAGs: recent progress and perspectives. Curr Opin Struct Biol 20:567–574

    Article  CAS  Google Scholar 

  3. Kaplan KL, Francis CW (2002) Direct thrombin inhibitors. Semin Hematol 39:187–196

    Article  CAS  Google Scholar 

  4. Farrell E, O’Brien FJ, Doyle P, Fischer J, Yannas I, Harley BA, O’Connell B, Prendergast PJ, Campbell VA (2006) A collagen-glycosaminoglycan scaffold supports adult rat mesenchymal stem cell differentiation along osteogenic and chondrogenic routes. Tissue Eng 12:459–468

    Article  CAS  Google Scholar 

  5. Tamura J (2001) Recent advances in the synthetic studies of glycosaminoglycans. Trends Glycosci Glycotech 13:65–89

    Article  Google Scholar 

  6. Suda Y, Marques D, Kermode JC, Kusumoto S, Sobel M (1993) Structural characterization of heparin’s binding domain for human platelets. Thromb Res 69:501–550

    Article  CAS  Google Scholar 

  7. Maccarana M, Casu B, Lindahl U (1993) Minimal sequence in heparin/heparan sulfate required for binding of basic fibroblast growth factor. J Biol Chem 268:23898–23905

    CAS  Google Scholar 

  8. Koshida S, Suda Y, Sobel M, Ormsby J, Kusumoto S (1999) Synthesis of heparin partial structures and their binding activities to platelets. Bioorg Med Chem Lett 9:3127–3132

    Article  CAS  Google Scholar 

  9. Hu YP, Lin SY, Huang CY, Zulueta MML, Liu JY, Chang Y, Hung SC (2011) Synthesis of 3-O-sulfonated heparan sulfate octasaccharides that inhibit the herpes simplex virus type 1 host–cell interaction. Nat Chem 3:557–563

    Article  CAS  Google Scholar 

  10. de Paz JL, Noti C, Seeberger PH (2006) Microarrays of synthetic heparin oligosaccharides. J Am Chem Soc 128:2766–2767

    Article  Google Scholar 

  11. Habuchi H, Habuchi O, Kimata K (1998) Biosynthesis of heparan sulfate and heparin: how are the multifunctional glycosaminoglycans built up? Trends Glycosci Glycotechnol 10:65–80

    Article  CAS  Google Scholar 

  12. Rawat M, Gama CI, Matson JB, Hsieh-Wilson LC (2008) Neuroactive chondroitin sulfate glycomimetics. J Am Chem Soc 130:2959–2961

    Article  CAS  Google Scholar 

  13. Suda Y, Arano A, Fukui Y, Koshida S, Wakao M, Nishimura T, Kusumoto S, Sobel M (2006) Immobilization and clustering of structurally defined oligosaccharides for sugar chips: an improved method for surface plasmon resonance analysis of protein-carbohydrate interactions. Bioconjug Chem 17:1125–1135

    Article  CAS  Google Scholar 

  14. Miura Y, Hoshino Y, Seto H (2016) Glycopolymer nanobiotechnology. Chem Rev 116:1673–1692

    Article  CAS  Google Scholar 

  15. Kobayashi K, Sumitomo H, Ina Y (1985) Synthesis and functions of polystyrene derivatives having pendant oligosaccharides. Polymer J 17:567–575

    Google Scholar 

  16. Cairo GW, Gestwicki JE, Kanai M, Kiessling LL (2002) Control of multivalent interactions by binding epitope density. J Am Chem Soc 124:1615–1619

    Article  CAS  Google Scholar 

  17. Miura Y, Yasuda K, Yamamoto K, Koike M, Nishida Y, Kobayashi K (2007) Inhibition of Alzheimer amyloid aggregation with sulfated glycopolymers. Biomacromol 8:2129–2134

    Article  CAS  Google Scholar 

  18. Sasaki K, Nishida Y, Uzawa H, Kobayashi K (2003) N-Acetyl-6-sulfo-D-glucosamine as a promising mimic of N-acetyl neuraminic acid. Bioorg Med Chem Lett 13:2821–2823

    Article  CAS  Google Scholar 

  19. Selkoe DJ (1994) Normal and abnormal biology of the beta-amyloid precursor protein. Annu Rev Nuerosci 17:489–517

    Google Scholar 

  20. Glenner GG, Wong CW (1984) Alzheimer’s disease and down’s syndrome: Sharing of a unique cerebrovascular amyloid fibril protein. Biochem Biophys Res Commun 122:1131–1135

    Article  CAS  Google Scholar 

  21. Levine HIII (1999) Quantification of b-sheet amyloid fibril structures with thioflavin T. Methods Enzymol 309:274–284

    Article  CAS  Google Scholar 

  22. Snow AD, Willmer J, Kisilevsky R (1987) Sulfated glycosaminoglycans: a common constituent of all amyloids? Lab Invest J Tech Methods Pathol 56:120–123

    CAS  Google Scholar 

  23. Hirsh J, Levine M (1992) Low molecular weight heparin. Blood 79:1–17

    CAS  Google Scholar 

  24. Bergamaschini L, Rossi E, Storini C, Pizzimenti S, Distaso M, Perego C, Luigi AD, Vergani C, de Simoni MG (2004) Peripheral treatment with enoxaparin, a low molecular weight heparin, reduces Plaques and β-amyloid accumulation in a mouse model of Alzheimer’s disease. J Neurosci 24:4181–4186

    Article  CAS  Google Scholar 

  25. Miura Y, Mizuno H (2010) Interaction analyses of amyloid BETA peptide (1-40) with glycosaminoglycan model polymers. Bull Chem Soc Jpn 83:1004–1009

    Article  CAS  Google Scholar 

  26. Nishimura Y, Shudo H, Seto H, Hoshino Y, Miura Y (2013) Syntheses of sulfated glycopolymers and analyses of their BACE-1 inhibitory activity. Bioorg Med Chem Lett 23:6390–6395

    Article  CAS  Google Scholar 

  27. Patey SJ, Edwards EA, Yates EA, Turnbull JE (2006) Heparin derivatives as inhibitors of BACE-1, the Alzheimer’s β-secretase, with reduced activity against factor Xa and other proteases. J Med Chem 49:6129–6132

    Article  CAS  Google Scholar 

  28. Fukuda T, Kawamura M, Mizuno H, Miura Y (2013) Glycosaminoglycan model polymers with poly (γ-glutamate) backbone to inhibit aggregation of β-amyloid peptide. Polymer J 45:359–362

    Article  CAS  Google Scholar 

  29. Miura Y, Onogi S, Fukuda T (2012) Syntheses of sulfo-glycodendrimers using click chemistry and their biological evaluation. Molecules 17:11877–11896

    Article  CAS  Google Scholar 

  30. Fukuda T, Matsumoto E, Onogi S, Miura Y (2010) Aggregation of Alzheimer amyloid β peptide (1–42) on the multivalent sulfonated sugar interface. Bioconjugate Chem 21:1079–1086

    Article  CAS  Google Scholar 

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Correspondence to Yoshiko Miura .

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Miura, Y., Fukuda, T., Seto, H., Hoshino, Y. (2018). Syntheses and Functions of Glycosaminoglycan Mimicking Polymers. In: Witczak, Z., Bielski, R. (eds) Coupling and Decoupling of Diverse Molecular Units in Glycosciences. Springer, Cham. https://doi.org/10.1007/978-3-319-65587-1_10

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