Boronic Acid-Functionalized Core–Shell–Shell Magnetic Composite Microspheres for the Selective Enrichment of Glycoprotein
Source abstract
Abstract
In this work, core-shell-shell-structured boronic acid-functionalized magnetic composite microspheres Fe3O4@SiO2@poly (methyl methacrylate-co-4-vinylphenylbornoic acid) (Fe3O4@SiO2@P(MMA-co-VPBA)) with a uniform size and fine morphology were synthesized. Here, Fe3O4 magnetic particles were prepared by a solvothermal reaction, whereas the Fe3O4@SiO2 microspheres with a core-shell structure were obtained by a sol-gel process. 3-(Trimethoxysilyl) propyl methacrylate (MPS)-modified Fe3O4@SiO2 was used as the seed in the emulsion polymerization of MMA and VPBA to form the core-shell-shell-structured magnetic composite microspheres. As the boronic acid groups on the surface of Fe3O4@SiO2@P(MMA-co-VPBA) could form tight yet reversible covalent bonds with the cis-1,2-diols groups of glycoproteins, the magnetic composite microspheres were applied to enrich a standard glycoprotein, horseradish peroxidase (HRP), and the results demonstrated that the composite microspheres have a higher affinity for the glycoproteins in the presence of the nonglycoprotein bovine serum albumin (BSA) over HRP. Additionally, different monomer mole ratios of MMA/VPBA were studied, and the results implied that using MMA as the major monomer could reduce the amount of VPBA with a similar glycoprotein enrichment efficiency but a lower cost.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Glycosylation and Glycoproteins Research · Microfluidic and Capillary Electrophoresis Applications · Advanced Proteomics Techniques and Applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Molecular Engineering of Polymers and Department of Macromolecular Science, Fudan University, 220 Handan Road, Shanghai 200433, China
State Key Laboratory of Genetic Engineering and School of Life Sciences, Fudan University, 220 Handan Road, Shanghai 200433, China
References (44)
Show source-provided references
1. Spiro R. G. · Glycobiology · 2002 · 12 · 43R10.1093/glycob/12.4.43R ↗
2. Dwek M. V. · Proteomics · 2001 · 1 · 75610.1002/1615-9861(200106)1:6<756::AID-PROT756>3.0.CO;2-X ↗
3. Ireland B. S. · Mol. Biol. Cell · 2008 · 19 · 241310.1091/mbc.e07-10-1055 ↗
4. Krishnamoorthy L. · ACS Chem. Biol. · 2009 · 4 · 71510.1021/cb900103n ↗
5. Kaji H. · Nat. Biotechnol. · 2003 · 21 · 66710.1038/nbt829 ↗
6. Xu Y. W. · Anal. Chem. · 2009 · 81 · 50310.1021/ac801912t ↗
7. Dell A. · Science · 2001 · 291 · 235110.1126/science.1058890 ↗
8. Bunkenborg J. · Proteomics · 2004 · 4 · 45410.1002/pmic.200300556 ↗
9. Hirabayashi J. · Glycoconjugate J. · 2004 · 21 · 3510.1023/B:GLYC.0000043745.18988.a1 ↗
10. Cummings R. D. · J. Biol. Chem. · 1982 · 257 · 1235
11. Zhang H. · Nat. Biotechnol. · 2003 · 21 · 66010.1038/nbt827 ↗
12. Wada Y. · Anal. Chem. · 2004 · 76 · 656010.1021/ac049062o ↗
13. Yu L. · Chem.—Eur. J. · 2009 · 15 · 1261810.1002/chem.200902370 ↗
14. Selman M. H. J. · Anal. Chem. · 2011 · 83 · 249210.1021/ac1027116 ↗
15. Alvarez-Manilla G. · J. Proteome Res. · 2006 · 5 · 70110.1021/pr050275j ↗
16. Zielinska D. F. · Cell · 2010 · 141 · 89710.1016/j.cell.2010.04.012 ↗
17. Sparbier K. · J. Biomol. Tech. · 2005 · 16 · 407
18. Zhou W. · Chem. Commun. · 2008 · 43 · 557710.1039/b808800d ↗
19. Cartwright S. J. · Biochem. J. · 1984 · 221 · 50510.1042/bj2210505 ↗
20. Liu X. C. · J. Mol. Recognit. · 1996 · 9 · 46210.1002/(SICI)1099-1352(199634/12)9:5/6<462::AID-JMR283>3.0.CO;2-G ↗
21. Bhatnagar P. K. · J. Chromatogr., B · 2008 · 863 · 23510.1016/j.jchromb.2008.01.003 ↗
22. Sun X. L. · Talanta · 2010 · 81 · 85610.1016/j.talanta.2010.01.029 ↗
23. Yang F. · J. Chromatogr., A · 2011 · 1218 · 919410.1016/j.chroma.2011.10.049 ↗
24. Lin Z. A. · Chem. Commun. · 2011 · 47 · 967510.1039/c1cc13082j ↗
25. Qi D. L. · Polym. Int. · 2007 · 56 · 20810.1002/pi.2130 ↗
26. Li W. H. · Macromolecules · 2000 · 33 · 435410.1021/ma9920691 ↗
27. Qu Y. Y. · Chem.—Eur. J. · 2012 · 18 · 905610.1002/chem.201103514 ↗
28. Qi D. W. · J. Phys. Chem. C · 2010 · 114 · 922110.1021/jp9114404 ↗
29. Zhang H. Y. · Chin. J. Chem. · 2011 · 29 · 83510.1002/cjoc.201190166 ↗
30. Ma W. F. · J. Polym. Sci., Part A: Polym. Chem. · 2011 · 49 · 272510.1002/pola.24705 ↗
31. Hofmann S. · J. Controlled Release · 2006 · 111 · 21910.1016/j.jconrel.2005.12.009 ↗
32. Laemmli U. K. · Nature · 1970 · 227 · 68010.1038/227680a0 ↗
33. Xuan S. H. · Chem. Mater. · 2009 · 21 · 507910.1021/cm901618m ↗
34. Gao R. X. · J. Mater. Chem. · 2011 · 21 · 1786310.1039/c1jm12414e ↗
35. Deng H. · Angew. Chem., Int. Ed. · 2005 · 44 · 278210.1002/anie.200462551 ↗
36. Xu X. · Adv. Mater. · 2006 · 18 · 328910.1002/adma.200601546 ↗
37. Liu J. · Angew. Chem., Int. Ed. · 2009 · 48 · 587510.1002/anie.200901566 ↗
38. Chen H. · Angew. Chem., Int. Ed. · 2010 · 49 · 60710.1002/anie.200904885 ↗
39. Qi D. · J. Phys. Chem. C · 2010 · 114 · 922110.1021/jp9114404 ↗
40. Cambre J. N. · Polymer · 2011 · 52 · 463110.1016/j.polymer.2011.07.057 ↗
41. De Sousa Delgado A. · Langmuir · 2001 · 17 · 438610.1021/la001701c ↗
42. Reimhult K. · Langmuir · 2008 · 24 · 869510.1021/la800224s ↗
43. Sparbier K. · J. Chromatogr., B · 2006 · 840 · 2910.1016/j.jchromb.2006.06.028 ↗
44. Tang J. · Proteomics · 2010 · 10 · 200010.1002/pmic.200900377 ↗