journal article·2014-07-23

Size-Exclusive Magnetic Graphene/Mesoporous Silica Composites with Titanium(IV)-Immobilized Pore Walls for Selective Enrichment of Endogenous Phosphorylated Peptides

Nianrong Sun, Chunhui Deng, Yan Li, Xiangmin Zhang

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Abstract

Developing an effective separation method is necessary for identifying low-abundant endogenous phosphorylated peptides with the removal of proteins. In this work, we prepared size-exclusive magnetic graphene/mesoporous silica composites with titanium(IV)-immobilized pore walls (denoted as Ti(4+)-MGMSs) for capturing endogenous phosphorylated peptides for mass spectrometry analysis. The introduction of hydrophilic polydopamine simplified the synthetic process of Ti(4+)-MGMSs, and the ordered mesoporous channels are beneficial to the trapping of endogenous phosphopeptides while large-size proteins are excluded. Furthermore, the magnetic performance greatly simplifies the entire process of enrichment. With all of the advances, the novel Ti(4+)-MGMSs present high enrichment efficiency either from the low concentration of β-casein tryptic digest (0.5 fmol/μL) or the mixture of β-casein tryptic digest and α-casein (or plus bovine serum albumin, with a mass ratio up to 1:500). Besides, Ti(4+)-MGMSs have also been successfully applied to enrich endogenous phosphorylated peptides from human serum and human saliva.
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Research context

OpenAlex topics: Advanced Proteomics Techniques and Applications · Mass Spectrometry Techniques and Applications · Advanced biosensing and bioanalysis techniques

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Chemistry and Institutes of Biomedical Sciences, Fudan University, Shanghai 200433, China

Pharmaceutical Analysis Department, School of Pharmacy, Fudan University, Shanghai 201203, China

Funding

Ministry of Education of the People's Republic of China · Ministry of Science and Technology of the People's Republic of China · National Natural Science Foundation of China · Shangai Leading Academic Discipline Project

References (24)

Show source-provided references
1. Schulte I. · Expert Rev. Mol. Diagn. · 2005 · 5 · 14510.1586/14737159.5.2.145 ↗
2. Diamandis E. P. · J. Proteome Res. · 2006 · 5 · 207910.1021/pr060225u ↗
3. Petricoin E. F. · Nat. Rev. Cancer · 2006 · 6 · 96110.1038/nrc2011 ↗
4. Petricoin E. F. · Lancet · 2002 · 359 · 57210.1016/S0140-6736(02)07746-2 ↗
5. Villanueva J. · J. Clin. Invest. · 2006 · 116 · 27110.1172/JCI26022 ↗
6. Rai A. J. · Proteomics · 2005 · 5 · 326210.1002/pmic.200401245 ↗
7. Hsieh S. Y. · Proteomics · 2006 · 6 · 318910.1002/pmic.200500535 ↗
8. Villanueva J. · Anal. Chem. · 2004 · 76 · 156010.1021/ac0352171 ↗
9. Johnson K. L. · Anal. Chem. · 2004 · 76 · 509710.1021/ac0497003 ↗
10. Yuan X. · J. Mass Spectrom. · 2005 · 40 · 17610.1002/jms.737 ↗
11. Zheng X. Y. · J. Chromatogr. A · 2006 · 1120 · 17310.1016/j.chroma.2006.01.098 ↗
12. Aristoteli L. P. · J. Proteome Res. · 2007 · 6 · 57110.1021/pr0602996 ↗
13. Yin P. · Proteomics · 2012 · 12 · 278410.1002/pmic.201200116 ↗
14. Hu L. H. · Anal. Chem. · 2009 · 81 · 9410.1021/ac801974f ↗
15. Qin H. Q. · Angew. Chem., Int. Ed. · 2011 · 50 · 1221810.1002/anie.201103666 ↗
16. Qin H. Q. · Chem. Commun. · 2012 · 48 · 96110.1039/C1CC15222J ↗
17. Zhu G. T. · J. Chromatogr. A · 2012 · 1224 · 1110.1016/j.chroma.2011.12.045 ↗
18. Liu S. S. · Angew. Chem., Int. Ed. · 2010 · 49 · 755710.1002/anie.201003602 ↗
19. Yin P. · Proteomics · 2013 · 13 · 224310.1002/pmic.201300066 ↗
20. Yan Y. H. · Anal. Chem. · 2013 · 85 · 848310.1021/ac401668e ↗
21. Sun N. R. · Anal. Chem. · 2014 · 86 · 224610.1021/ac404103r ↗
22. Iorgulescu G. · J. Med. Life · 2009 · 2 · 303
23. Dodds M. W. · J. Dent. · 2005 · 33 · 22310.1016/j.jdent.2004.10.009 ↗
24. Lee Y. H. · Am. J. Dent. · 2009 · 22 · 241