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Materials-Metals 2017

Page 33

November 16-17, 2017 Paris, France

13

th

Annual Conference on

Materials Science, Metal and Manufacturing

Journal of Materials Science and Nanotechnology

Volume 1 Issue 2

Kaoru Tamada et al., Mater Sci Nanotechnol 2017, 1:2

High-resolution imaging of a cell-attached

nanointerface using a gold-nanoparticle two-

dimensional sheet

Kaoru Tamada

1

, Shihomi Masuda

1

, Sou Ryuzaki

1

, Pangpang Wang

1

, Koichi

Okamoto

1

, Thasaneeya Kuboki

1

, Satoru Kidoaki

1

, Yuhki Yanase

2

and

Eiji

Usukura

3

1

Kyushu University, Japan

2

Hiroshima University, Japan

3

Nagoya University, Japan

T

his paper reports our original technique for visualizing

cell-attached nanointerfaces with extremely high axial

resolution (a few tens of nanometers) using collectively excited

localized surface plasmon resonance (LSPR) on a self-assembled

metal nanoparticle sheet. Oleylamine-capped gold NPs (AuOA,

13nm) and myristate-capped silver nanoparticles (AgMy, 5nm)

were self-assembled at an air-water interface and transferred on

hydrophobic cover slip by Langmuir-Schaefer method to be an

imaging substrate. This self-assembled metal nanoparticle sheet

can confine and enhance the fluorescence at the nanointerface.

Test experiments on rat basophilic leukemia (RBL-2H3) cells

with fluorescence-labeled actin filaments revealed high axial and

lateral resolution in the image of focal adhesionat the cell-attached

interface even under a regular epifluorescence microscope,

which produced higher quality images than those captured

under a total internal reflection fluorescence (TIRF) microscope.

Recently, the demand for super-resolution fluorescence

microscopy is increasing in the field of cell biology because of the

requirement to investigate molecular-level dynamic reactions in

or near cells. The super-resolution microscopy techniques, such

as confocal laser microscopy, STED, SIM, and PALM/STORM,

have a significant advantage in their lateral resolution but are

not as advantageous in either their axial resolution or temporal

resolution because of their scanning criteria. TIRF microscopy

provides the highest axial and temporal resolution compared

with the other super-resolution microscope systems, although

the imaging area is still 100-200 nm from the top surface of

a cover slip. The common problem of these state-of-the-art

technology is the cost of the apparatus, which prevents it from

being standard equipment in basic laboratories. On contrast,

our non-scanning-type, high-resolution imaging method using

nanoparticle LSPR is very user-friendly and effective tool for

monitoring nano interfacial phenomena. This technique will

open the possibility for all biochemists and medical scientists

to perform state-of-the-art molecular imaging using their own

conventional microscope.

Figure:

(a) Schematic drawing of the depth of the LSPR on the

AuOA sheet and evanescent fields on glass. (b) Fluorescence

images of FITC-labeled actin filaments in RBL-2H3 cells on the

AuOA sheet (left) and on glass(right).

Recent Publications

• S Masuda et. al. (2017) High-resolution imaging of a cell-

attached nanointerface using a gold-nanoparticle two-

dimensional sheet. Sci. Rep. 7:3720.

• M Toma et. al. (2011) Collective plasmon modes excited

on a silver nanoparticle 2D crystalline sheet. Phys. Chem.

Chem. Phys. 13(16):7459-7466.

• D Tanaka et. al. (2015) Characteristics of localized surface

plasmons excited on mixed monolayers composed of self-

assembled Ag and Au nanoparticles.

• K Okamoto et. al. (2016) Electromagnetically induced

transparency of a plasmonic metamaterial light absorber

based on multilayered metallic nanoparticle sheets. Sci. Rep.

6:36165

Biography

Kaoru Tamada is a Scientist in the field of Surface Science and Nanoscience.

After 7 years of R&D experience in industry, she joined Prof. Hyuk Yu’s lab in

Univ. of Wisconsin-Madison and obtained Dr. Sci. at Nara Women’s University

in 1994. After Postdoc experience in Riken, she worked as a Senior Scientist in

AIST Japan for 10 years. During this period, she joined ANU, MPIP and NUS as

a Visiting Scientist. She joined TokyoTECH in 2005 as an Associate Professor,

and RIEC, Tohoku Univ. in 2007 as a Professor. She moved to IMCE, Kyushu

Univ. in 2011, and was promoted to Vice President from 2017. Her research

interest is self-assembly of molecules and nanomaterials, plasmonics, and their

bio-sensor and bio-imaging applications.

tamada@ms.ifoc.ykushu-u.ac.jp