journal article·2013-02-13

Two-in-One Strategy for Effective Enrichment of Phosphopeptides Using Magnetic Mesoporous γ-Fe2O3 Nanocrystal Clusters

Yuting Zhang, Lulu Li, Wanfu Ma, Ying Zhang, Meng Yu, Jia Guo, Haojie Lu, Changchun Wang

Publisher page

Abstract

Designed with a two-in-one strategy, the magnetic mesoporous γ-Fe(2)O(3) nanocrystal clusters (m-γ-Fe(2)O(3)) have been successfully prepared for integrating the functions of effective enrichment and quick separation of phosphopeptides into a single architecture. First, the mesoporous Fe(3)O(4) nanocrystal clusters (mFe(3)O(4)) were synthesized by solvothermal reaction and then were subjected to calcination in air to form m-γ-Fe(2)O(3). The obtained m-γ-Fe(2)O(3) have spherical morphology with uniform particle size of about 200 nm and mesoporous structure with the pore diameter of about 9.7 nm; the surface area is as large as 117.8 m(2)/g, and the pore volume is 0.34 cm(3)/g. The m-γ-Fe(2)O(3) possessed very high magnetic responsiveness (Ms = 78.8 emu/g, magnetic separation time from solution is less than 5 s) and were used for the selective enrichment of phosphopeptides for the first time. The experimental results demonstrated that the m-γ-Fe(2)O(3) possessed high selectivity for phosphopeptides at a low molar ratio of phosphopeptides/nonphosphopeptides (1:100), high sensitivity (the detection limit was at the fmol level), high enrichment recovery (as high as 89.4%), and excellent speed (the enrichment can be completed in 10 min). Moreover, this material is also quite effective for enrichment of phosphopeptides from the real sample (drinking milk), showing great potential in the practical application.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Advanced Proteomics Techniques and Applications · Advanced biosensing and bioanalysis techniques · Machine Learning in Bioinformatics

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, Laboratory of Advanced Materials, Fudan University, Shanghai 200433, China

Department of Chemistry and Institutes of Biomedical Sciences, Fudan University, Shanghai 200032, People’s Republic of China

References (39)

Show source-provided references
1. Ptacek J. · Nature · 2005 · 438 · 67910.1038/nature04187 ↗
2. Olsen J. V. · Cell · 2006 · 127 · 63510.1016/j.cell.2006.09.026 ↗
3. Ndassa Y. M. · J. Proteome Res. · 2006 · 5 · 278910.1021/pr0602803 ↗
4. Posewitz M. C. · Anal. Chem. · 1999 · 71 · 288310.1021/ac981409y ↗
5. Feng S. · Mol. Cell. Proteomics · 2007 · 6 · 165610.1074/mcp.T600071-MCP200 ↗
6. Hu L. H · Anal. Chem. · 2009 · 81 · 9410.1021/ac801974f ↗
7. Larsen M. R. · Mol. Cell. Proteomics · 2005 · 4 · 87310.1074/mcp.T500007-MCP200 ↗
8. Kweon H. K. · Anal. Chem. · 2006 · 78 · 174310.1021/ac0522355 ↗
9. Nata I. F. · ACS Appl. Mater. Interfaces · 2011 · 3 · 334210.1021/am200453e ↗
10. Singh A. · ACS Appl. Mater. Interfaces · 2011 · 3 · 84210.1021/am101196v ↗
11. Li Y. · ACS Appl. Mater. Interfaces · 2011 · 3 · 330810.1021/am2007855 ↗
12. Tan F. · J. Proteome Res. · 2008 · 7 · 107810.1021/pr700655d ↗
13. Zhao L. · J. Am. Soc. Mass Spectrom. · 2008 · 19 · 117610.1016/j.jasms.2008.04.027 ↗
14. Li Y. C. · Anal. Chem. · 2007 · 79 · 751910.1021/ac0711440 ↗
15. Chen C. T. · Anal. Chem. · 2005 · 77 · 591210.1021/ac050831t ↗
16. Li Y. · J. Proteome Res. · 2007 · 6 · 449810.1021/pr070167s ↗
17. Tang J. · J. Chromatogr., A · 2010 · 1217 · 219710.1016/j.chroma.2010.02.008 ↗
18. Ma W. F. · ACS Nano · 2012 · 6 · 317910.1021/nn3009646 ↗
19. Nelson C. A. · Chem. Commun. · 2009 · 43 · 660710.1039/b908788e ↗
20. Nelson C. A. · Anal. Chem. · 2010 · 82 · 719310.1021/ac100877a ↗
21. Lee A. · Rapid Commun. Mass Spectrom. · 2008 · 22 · 256110.1002/rcm.3652 ↗
22. Huang Y. · Anal. Biochem. · 2011 · 408 · 1910.1016/j.ab.2010.08.002 ↗
23. Han L. · J. Colloid Interface Sci. · 2008 · 318 · 31510.1016/j.jcis.2007.10.026 ↗
24. Malik A. S. · J. Mater. Chem. · 2003 · 13 · 212310.1039/b303551d ↗
25. Long J. W. · J. Am. Chem. Soc. · 2004 · 126 · 1687910.1021/ja046044f ↗
26. Jiao F. · Angew. Chem., Int. Ed. · 2004 · 116 · 608410.1002/ange.200460826 ↗
27. Tian B. Z. · J. Am. Chem. Soc. · 2004 · 126 · 86510.1021/ja037877t ↗
28. Jiao F. · J. Am. Chem. Soc. · 2006 · 128 · 546810.1021/ja0584774 ↗
29. Kong A. G. · Mater. Lett. · 2008 · 62 · 94310.1016/j.matlet.2007.07.015 ↗
30. Luo B. · ACS Nano · 2011 · 5 · 142810.1021/nn103213y ↗
31. Ge J. P. · Angew. Chem., Int. Ed. · 2007 · 46 · 434210.1002/anie.200700197 ↗
32. Wu G. · J. Alloys Compd. · 2010 · 504 · 37110.1016/j.jallcom.2010.05.119 ↗
33. Jiao F. · J. Am. Chem. Soc. · 2006 · 128 · 1290510.1021/ja063662i ↗
34. deFaria D. L. A. · J. Raman Spectrosc. · 1997 · 28 · 87310.1002/(SICI)1097-4555(199711)28:11<873::AID-JRS177>3.0.CO;2-B ↗
35. Yao D. · Anal. Chem. · 2001 · 73 · 283610.1021/ac001404c ↗
36. Liu Z. · J. Proteome Res. · 2010 · 9 · 22710.1021/pr900528j ↗
37. Li Y. C. · Anal. Chem. · 2007 · 79 · 751910.1021/ac0711440 ↗
38. Cheng G. · Chem. Commun. · 2011 · 47 · 573210.1039/c1cc10533g ↗
39. Sturm M. · Adv. Funct. Mater. · 2008 · 18 · 238110.1002/adfm.200800215 ↗