Investigation of molecular surfaces with time-of-flight secondary ion mass spectrometry

被引:0
|
作者
Aoyagi, Satoka [1 ]
Namekawa, Koki [2 ]
Yamamoto, Kenichiro [3 ]
Sakai, Kiyotaka [2 ]
Kato, Nobuhiko [4 ]
Kudo, Masahiro [4 ]
机构
[1] Shimane Univ, Fac Life & Environm Sci, Matsue, Shimane 6908504, Japan
[2] Waseda Univ, Dept Chem Engn, Shinjuku Ku, Tokyo 1698555, Japan
[3] Waseda Univ, Waseda Inst Adv Study, Shinjuku Ku, Tokyo 1698050, Japan
[4] Seikei Univ, Fac Sci & Technol, Tokyo 1808633, Japan
关键词
TOF-SIMS; C(60)(+); polypeptide; protein; orientation; TOF-SIMS; BOMBARDMENT;
D O I
10.1002/sia.3613
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
TOF-SIMS is a promising technique for evaluating biodevices due to its ultrahigh surface sensitivity. Since a cluster ion source such as C(60)(+) provides low collision energy per atom, time-of-flight secondary ion mass spectrometry (TOF-SIMS) with the cluster ion is useful for detecting the uppermost surface of molecules immobilized on a substrate, and therefore, enables the evaluation of the orientation of these immobilized biomolecules. Effects of TOF-SIMS with C(60)(+) were investigated in this study. A relatively small protein, lysozyme, and polypeptides having five amino acid residues, Leu-enkephalin and Met-enkephalin, were employed as model samples. The protein and the polypeptides were immobilized on aminosilanized-indium-tin oxide (ITO) coated glass plates at their N-terminal residues by covalent bonding. The aminosilanized-ITO plate without protein or polypeptide was also prepared as a control sample. After freeze-drying, the samples were measured with TOF-SIMS using gallium and C(60)(+) cluster ion sources, and then TOF-SIMS spectra were analyzed to select peaks specific to each biomolecule by a comparison between the samples. As a result, the C(60)(+) primary ion source showed advantages in evaluating biomolecules, because more peaks at a higher mass generated from the biomolecules can be obtained using C(60)(+) than Ga(+) or Au(3)(+) as the primary ion source, although no difference was detected between the two polypeptide samples under the current measurement conditions. Copyright (C) 2010 John Wiley & Sons, Ltd.
引用
收藏
页码:1593 / 1597
页数:5
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