Hiroshi Nakashima
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Hiroshi Nakashima has a total of 5 co-authors. Here are the top co-authors by number of shared publications:
- Kazuaki Furukawa
NTT Basic Research Laboratories, NTT Corporation, 3-1 Morinosato Wakamiya, Atsugi, Kanagawa 243-0198, Japan
3 shared publications Keiichi Torimitsu
Materials Science Research Laboratory, NTT Basic Research Laboratories, NTT Corporation, 3-1 Morinosato Wakamiya, Atsugi, Kanagawa 243-0198, Japan
3 shared publicationsYoshiaki Kashimura
Materials Science Research Laboratory, NTT Basic Research Laboratories, NTT Corporation, 3-1 Morinosato Wakamiya, Atsugi, Kanagawa 243-0198, Japan
3 shared publications- Koji Sumitomo
University of Hyogo
1 shared publication - Youichi Shinozaki
Visual Research Project, Tokyo Metropolitan Institute of Medical Science, Tokyo, Japan
1 shared publication
Latest Publications
- 13 July 2010
- Published by American Chemical Society (ACS) in Langmuir
- Vol. 26 (15) , 12716-12721
Pattern Formation and Molecular Transport of Histidine-Tagged GFPs Using Supported Lipid Bilayers
We fabricated a heterogeneous supported lipid bilayer (SLB) by employing binary lipid mixtures comprising a saturated acyl chain DSPC and an unsaturated acyl chain nickel-chelating lipid. By using the specific adsorption properties of histidine-tagged proteins (His-tagged GFPs) in relation to nickel-chelating lipids, we demonstrated protein pattern formation on the SLB corresponding to the phase separation pattern of the SLB. In addition, by using a lipid mixture consisting of an unsaturated acyl chain DOPC and a nickel-chelating lipid, and His-tagged GFPs, we succeeded in transporting the proteins along a hydrophilic micropattern on a SiO2 substrate. The protein transport is induced by the self-spreading behavior of a fluid SLB with a kinetic spreading coefficient β = 10.4 μm2 s−1. This method provides a guide for strategically carrying various biomolecules to specific positions by using a soft biointerface on a solid surface. In addition, the results demonstrate the importance of using techniques that allow the controlled manipulation of biomolecules based on the static or dynamic properties of the SLB platform.
- 13 July 2010
- Published by American Chemical Society (ACS) in Langmuir
- Vol. 26 (15) , 12716-12721
Pattern Formation and Molecular Transport of Histidine-Tagged GFPs Using Supported Lipid Bilayers
We fabricated a heterogeneous supported lipid bilayer (SLB) by employing binary lipid mixtures comprising a saturated acyl chain DSPC and an unsaturated acyl chain nickel-chelating lipid. By using the specific adsorption properties of histidine-tagged proteins (His-tagged GFPs) in relation to nickel-chelating lipids, we demonstrated protein pattern formation on the SLB corresponding to the phase separation pattern of the SLB. In addition, by using a lipid mixture consisting of an unsaturated acyl chain DOPC and a nickel-chelating lipid, and His-tagged GFPs, we succeeded in transporting the proteins along a hydrophilic micropattern on a SiO2 substrate. The protein transport is induced by the self-spreading behavior of a fluid SLB with a kinetic spreading coefficient β = 10.4 μm2 s−1. This method provides a guide for strategically carrying various biomolecules to specific positions by using a soft biointerface on a solid surface. In addition, the results demonstrate the importance of using techniques that allow the controlled manipulation of biomolecules based on the static or dynamic properties of the SLB platform.
- 29 April 2008
- Published by American Chemical Society (ACS) in Langmuir
- Vol. 24 (11) , 5654-5658
Self-Assembly of Gold Nanorods Induced by Intermolecular Interactions of Surface-Anchored Lipids
Surface-modified gold nanorods (Au NRs) with 1,2-dipalmitoyl-sn-glycero-3-phosphothioethanol (DPPTE) were synthesized, and their self-assembled structures on a silicon substrate were observed using a scanning electron microscope (SEM). The Au NR−DPPTE complex formed characteristic one- and two-dimensional self-assemblies induced by intermolecular interactions of surface-anchored lipids via simple drying process. The interparticle distance between neighboring NRs was uniform at around 5.0 nm, which was consistent with the thickness of the lipid bilayer. Furthermore, we observed the anisotropic configurations of the NR complex, preferentially oriented in a lateral or perpendicular fashion, in a two-dimensional assembled structure dependent on the interfacial hydrophilicity or hydrophobicity of the silicon surface.
- 29 April 2008
- Published by American Chemical Society (ACS) in Langmuir
- Vol. 24 (11) , 5654-5658
Self-Assembly of Gold Nanorods Induced by Intermolecular Interactions of Surface-Anchored Lipids
Surface-modified gold nanorods (Au NRs) with 1,2-dipalmitoyl-sn-glycero-3-phosphothioethanol (DPPTE) were synthesized, and their self-assembled structures on a silicon substrate were observed using a scanning electron microscope (SEM). The Au NR−DPPTE complex formed characteristic one- and two-dimensional self-assemblies induced by intermolecular interactions of surface-anchored lipids via simple drying process. The interparticle distance between neighboring NRs was uniform at around 5.0 nm, which was consistent with the thickness of the lipid bilayer. Furthermore, we observed the anisotropic configurations of the NR complex, preferentially oriented in a lateral or perpendicular fashion, in a two-dimensional assembled structure dependent on the interfacial hydrophilicity or hydrophobicity of the silicon surface.
- 2 January 2007
- Published by Royal Society of Chemistry (RSC) in Chemical Communications
- No. 10,p. 1080-1082
Anisotropic assembly of gold nanorods assisted by selective ion recognition of surface-anchored crown ether derivatives
Gold nanorods (NRs) mixed with crown ether derivatives exhibited the efficient and selective recognition of Na+ and K+ ions, which were detected by localized surface plasmon absorption in response to dispersed and aggregated gold NRs. Furthermore, in the aggregates preferential end-to-end or side-to-side assembly of NRs was observed which was dependent on the additive concentration.
- 2 January 2007
- Published by Royal Society of Chemistry (RSC) in Chemical Communications
- No. 10,p. 1080-1082
Anisotropic assembly of gold nanorods assisted by selective ion recognition of surface-anchored crown ether derivatives
Gold nanorods (NRs) mixed with crown ether derivatives exhibited the efficient and selective recognition of Na+ and K+ ions, which were detected by localized surface plasmon absorption in response to dispersed and aggregated gold NRs. Furthermore, in the aggregates preferential end-to-end or side-to-side assembly of NRs was observed which was dependent on the additive concentration.