Facile Preparation of Core-Shell Magnetic Metal Organic Framework Nanoparticles for the Selective Capture of Phosphopeptides

被引:191
作者
Chen, Yajing [1 ]
Xiong, Zhichao [1 ]
Peng, Li [1 ]
Gan, Yangyang [1 ]
Zhao, Yiman [1 ]
Shen, Jie [1 ]
Qian, Junhong [1 ]
Zhang, Lingyi [1 ]
Zhang, Weibing [1 ]
机构
[1] E China Univ Sci & Technol, Shanghai Key Lab Funct Mat Chem, Dept Chem & Mol Engn, Shanghai 200237, Peoples R China
基金
中国国家自然科学基金;
关键词
magnetic nanoparticles; metal-organic framework (MOF); phosphorylated peptides; mass spectrum; size-exclusion; ION AFFINITY-CHROMATOGRAPHY; MALDI-TOF MS; PHOSPHOPROTEOME ANALYSIS; MASS-SPECTROMETRY; PHOSPHORYLATED PEPTIDES; MONOLITHIC CAPILLARY; EFFECTIVE ENRICHMENT; IN-VIVO; SEPARATION; MICROSPHERES;
D O I
10.1021/acsami.5b03335
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
In regard to the phosphoproteome, highly specific and efficient capture of heteroideous kinds of phosphopeptides from intricate biological sample attaches great significance to comprehensive and in-depth phosphorylated proteomics research. However, until now, it has been a challenge. In this study, a new-fashioned porous immobilized metal ion affinity chromatography (IMAC) material was designed and fabricated to promote the selectivity and detection limit for phosphopeptides by covering a metal-organic frameworks (MOFs) shell onto Fe3O4 nanoparticles, taking advantage of layer-by-layer method (the synthesized nanoparticle denoted as Fe3O4@MIL-100 (Fe)). The thick layer renders the nanoparticles with perfect hydrophilic character, super large surface area, large immobilization of the Fe3+ ions and the special porous structure. Specifically, the as-synthesized MOF-decorated magnetic nanoparticles own an ultra large surface area which is up to 168.66 m(2) g(-1) as well as two appropriate pore sizes of 1.93 and 3.91 nm with a narrow grain-size distribution and rapid separation under the magnetic circumstance. The unique features vested the synthesized nanoparticles an excellent ability for phosphopeptides enrichment with high selectivity for beta-casein (molar ratio of beta-casein/BSA, 1:500), large enrichment capacity (60 mg g(-1)), low detection limit (0.5 fmol), excellent phosphopeptides recovery (above 84.47%), fine size-exclusion of high molecular weight proteins, good reusability, and desirable batch-to-batch repeatability. Furthermore, encouraged by the experimental results, we successfully performed the as-prepared porous IMAC nanoparticle in the specific capture of phosphopeptides from the human serum (both the healthy and unhealthy) and nonfat milk, which proves itself to be a good candidate for the enrichment and detection of the low-abundant phosphopeptides from complicated biological samples.
引用
收藏
页码:16338 / 16347
页数:10
相关论文
共 53 条
[21]   Ti4+-Immobilized Magnetic Composite Microspheres for Highly Selective Enrichment of Phosphopeptides [J].
Ma, Wanfu ;
Zhang, Ying ;
Li, Lulu ;
Zhang, Yuting ;
Yu, Meng ;
Guo, Jia ;
Lu, Haojie ;
Wang, Changchun .
ADVANCED FUNCTIONAL MATERIALS, 2013, 23 (01) :107-115
[22]   Synthesis of Fe3O4-graphene-TiO2 ternary composite networks for enhanced capture of phosphopeptides [J].
Min, Qianhao ;
Zhang, Xiaoxia ;
Zhang, Hongyi ;
Zhou, Fang ;
Zhu, Jun-Jie .
CHEMICAL COMMUNICATIONS, 2011, 47 (42) :11709-11711
[23]   Strong cation exchange (SCX) based analytical methods for the targeted analysis of protein post-translational modifications [J].
Mohammed, Shabaz ;
Heck, Albert J. R. .
CURRENT OPINION IN BIOTECHNOLOGY, 2011, 22 (01) :9-16
[24]   Characterization of a TiO2 enrichment method for label-free quantitative phosphoproteomics [J].
Montoya, Alex ;
Beltran, Luisa ;
Casado, Pedro ;
Rodriguez-Prados, Juan-Carlos ;
Cutillas, Pedro R. .
METHODS, 2011, 54 (04) :370-378
[25]   Hydrogen storage in metal-organic frameworks [J].
Murray, Leslie J. ;
Dinca, Mircea ;
Long, Jeffrey R. .
CHEMICAL SOCIETY REVIEWS, 2009, 38 (05) :1294-1314
[26]   Large-scale analysis of in vivo phosphorylated membrane proteins by immobilized metal ion affinity chromatography and mass spectrometry [J].
Nühse, TS ;
Stensballe, A ;
Jensen, ON ;
Peck, SC .
MOLECULAR & CELLULAR PROTEOMICS, 2003, 2 (11) :1234-1243
[27]   Global, in vivo, and site-specific phosphorylation dynamics in signaling networks [J].
Olsen, Jesper V. ;
Blagoev, Blagoy ;
Gnad, Florian ;
Macek, Boris ;
Kumar, Chanchal ;
Mortensen, Peter ;
Mann, Matthias .
CELL, 2006, 127 (03) :635-648
[28]   Enrichment of phosphopeptides by Fe3+-immobilized mesoporous nanoparticles of MCM-41 for MALDI and nano-LC-MS/MS analysis [J].
Pan, Chensong ;
Ye, Mingliang ;
Liu, Yuge ;
Feng, Shun ;
Jiang, Xiaogang ;
Han, Guanghui ;
Zhu, Junjie ;
Zou, Hanfa .
JOURNAL OF PROTEOME RESEARCH, 2006, 5 (11) :3114-3124
[29]   Global analysis of protein phosphorylation in yeast [J].
Ptacek, J ;
Devgan, G ;
Michaud, G ;
Zhu, H ;
Zhu, XW ;
Fasolo, J ;
Guo, H ;
Jona, G ;
Breitkreutz, A ;
Sopko, R ;
McCartney, RR ;
Schmidt, MC ;
Rachidi, N ;
Lee, SJ ;
Mah, AS ;
Meng, L ;
Stark, MJR ;
Stern, DF ;
De Virgilio, C ;
Tyers, M ;
Andrews, B ;
Gerstein, M ;
Schweitzer, B ;
Predki, PF ;
Snyder, M .
NATURE, 2005, 438 (7068) :679-684
[30]   Metal-organic frameworks as potential multi-carriers of drugs [J].
Rojas, Sara ;
Wheatley, Paul S. ;
Quartapelle-Procopio, Elsa ;
Gil, Barbara ;
Marszalek, Bartosz ;
Morris, Russell E. ;
Barea, Elisa .
CRYSTENGCOMM, 2013, 15 (45) :9364-9367