Hostname: page-component-76fb5796d-skm99 Total loading time: 0 Render date: 2024-04-26T14:45:43.051Z Has data issue: false hasContentIssue false

Atomic Level Analysis of Amino Acids by the Scanning Atom Probe

Published online by Cambridge University Press:  31 January 2011

Osamu Nishikawa
Affiliation:
nisikawa@neptune.kanazawa-it.ac.jpprof_osamu_nishikawa@hotmail.com, Kanazawa Institute of Technology, 7-1 Ohgigaoka, Nonoichi, Ishikawa, 921-8501, Japan, +81-76-248-9473, +81-76-294-6717
Masahiro Taniguchi
Affiliation:
taniguchi@neptune.kanazawa-it.ac.jp, Kanazawa Institute of Technology, Biochemistry, Nonoichi, Japan
Atsushi Ikai
Affiliation:
ikai.a.aa@m.titech.ac.jp, Tokyo Institute of Technology, Biodynamics, Yokohama, Japan
Get access

Abstract

Atom probe (AP) is known to be a unique instrument that makes possible to mass analyze a specimen at atomic level. However, its application is mostly limited to metals and semiconductors because the AP analysis proceeds by field evaporating surface atoms applying the high field, 20-40 V/nm, on the specimen surface. In order to generate such a high field the analyzed area is an apex of a sharp tip. Metals and semiconductors can be formed in such a sharp tip easily. However, the formation of a sharp organic and bio molecule tip is not easy. Thus, we introduced a funnel shaped micro extraction electrode that scans over a specimen surface and confines the high field in a narrow space between the micro open hole at the apex of the electrode and a micro protrusion on a specimen surface. Thus, this type of the AP is named as scanning atom probe (SAP). Then, organic and bio molecules can be deposited on the micro protrusion on the specimen surface. The AP analysis of metals indicates that the field evaporation of metal atoms proceeds one atom by one atom implying that the binding between metal atoms are uniform and non-directional. On the other hand most atoms of non-metallic specimens are field evaporated as clustering atoms. For example, doubly charged thiophene monomers are detected when polythiophene is analyzed. This indicates that one sulfur and four carbon atoms are strongly bound. Similarly, the mass spectra of highly pure single walled carbon nano tubes (SWCNT) exhibit sharp mass peaks of C2+ and C+ indicating that carbon atoms are bound by non-directional strong bonds. This implies that the unique feature of the AP is not only in the identification of individual ion but also in the investigation of binding states of the atoms forming the materials. For the present analysis amino acids are deposited on a small ball of the SWCNT fibers in order to avoid the catalytic reaction of metals. The SWCNT ball is dipped in a solution of sample molecules. The glycine solution is made by dissolving 1 gram of glycine in 15 ml pure water. Cystine, leucine and methionine solutions are made by dissolving 50 mg of the molecules in 1 ml of 0.1 N HCl. Discrimination of the carbon ions of the SWCNT from the fragment ions of the molecules is relatively easy because nearly all of the SWCNT carbon ions are detected as C2+ and C+. Glycine is the smallest amino acid formed by a carboxy group, an amino group and a CH2 group. Thus, it is assumed that the analysis will provide a guideline for the analysis of larger molecule. However, the identification of fragments ions is not easy because many different fragments have the same mass such as CH3 and NH. This indicates that mass analyzer for the bio-molecules requires a mass spectrometer with the mass resolution m/Δm higher than 10,000. The characteristic mass spectra of the amino acids and the structure of a new SAP with a position sensitive ion detector with a spiral delay line will be presented.

Type
Research Article
Copyright
Copyright © Materials Research Society 2010

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1 Nishikawa, O. and Kimoto, M. Appl. Surf. Sci. 76/77, 424 (1994).Google Scholar
2 Nishikawa, O. Ohtani, Y. Maeda, K. Ma, Watanabe, M. and Tanaka, K. Mater. Char., 44, 29 (2000).Google Scholar
3 Nishikawa, O. and Taniguchi, M. Chinese J. Phys. 43, No. I-II, 111 (2006).Google Scholar
4 Nishikawa, Osamu, Taniguchi, Masahiro and Ikai, Atsushi, to be published in Appl. Surf. Sci. (2009).Google Scholar
5 Nishikawa, Osamu and Taniguchi, Masahiro, to be published in J. Vac. Sci. Technol. A27 (2009).Google Scholar
6 Seidman, David N. and Stiller, Krystyna, MRS Bulletin, eda, 34, 717 (2009).Google Scholar
7 Kelly, Thomas F. Nishikawa, Osamu, Panitz, John A. and Prosa, Ty J. MRS Bulletin, 34, 744 (2009).Google Scholar