Immobilization of histidine-tagged proteins by magnetic nanoparticles encapsulated with nitrilotriacetic acid (NTA)-phospholipids micelle

被引:33
作者
Lim, Yong Talk
Lee, Kun Yeong
Lee, Kwangyeol
Chung, Bong Hyun
机构
[1] Korea Res Inst Biosci & Biotechnol, Bionanotechnol Res Ctr, Taejon 305333, South Korea
[2] Korea Univ, Dept Chem, Seoul 136701, South Korea
关键词
immobilization of proteins; magnetic nanoparticles; phospholipids micelle; NTA-phospholipids; fluorescent proteins;
D O I
10.1016/j.bbrc.2006.03.209
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We described the development of functionalized magnetic nanoparticles (MNPs) with PEG-modification, a phospholipids micelle coating, and their use in manipulating histidine-tagged proteins. Highly monodisperse MNPs were synthesized in an organic solvent and could be phase-transferred into an aqueous solution by encapsulating the nanoparticles with a phospholipids micelle. The phospholipids micelle coating rendered the nanoparticles highly water-soluble, and the functional groups of the phospholipids coating allowed for the bioconjugation of various moieties, such as fluorescent molecules and engineered proteins. Functionalized phospholipids, such as nitrilotriacetic acid (NTA)-phospholipids, caused the MNPs to bind and allowed for manipulation of histidine-tagged proteins. Due to their high surface/volume ratio, the MNPs showed better performance (about 100 times higher) in immobilizing engineered proteins than conventional micrometer-sized beads. This demonstrates that MNPs coated with phospholipids micelle can be a versatile platform for the effective manipulation of various kinds of engineered proteins, which is very important in the field of proteomics. It is expected that a combination of MNPs with optical fluorescent molecules can find applications in bimodal (magnetic and optical) molecular imaging nanoprobes. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:926 / 930
页数:5
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