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Name (Title):<br />
Jun Nakanishi (MANA Independent Scientist)<br />
Affiliation:<br />
International Center for Materials Nanoarchitectonics (MANA), NIMS<br />
Address:<br />
1-1 Namiki Tsukuba, Ibaraki 305-0044, JAPAN<br />
Email: NAKANISHI.Jun@nims.go.jp<br />
Home Page: http://www.nims.go.jp/mana/members/young_scientist/j_nakanishi/index.html<br />
Presentation Title:<br />
Photoresponsive Biointerfaces for Cell Analysis<br />
<strong>Abstract</strong>:<br />
Biointerface is an interface between biomolecules and materials. We have been developing<br />
photoresponsive biointerfaces for controlling cellular functions as well as for engineering tissue<br />
mimics in vitro.<br />
Photoactivatable cell culture substrate. [1] Activities of the cells are highly dependent on their<br />
microenvironment, as can be imagined from the complex architecture of tissues and organs.<br />
However, most cell researches have been conducted on normal plastic or glass dish, whereon<br />
cells were attached quite randomly. We have developed several photoactivatable cell culture<br />
substrates that changed from non-cell-adhesive to cell adhesive in response to light (Figure 1a).<br />
Based on this feature, we were able to produce arbitral cell patterns by controlled irradiation.<br />
Furthermore, we succeeded in inducing cell migration and proliferation by irradiation during cell<br />
cultivation.<br />
Photoresponsive nanocarrier. [2] Concentrations of biomolecules such as hormones and proteins in<br />
living system are strictly controlled both in time and space. Therefore, it is important to deliver<br />
such biomolecules at will not only for therapeutic purposes but also for studying intertwined<br />
inter- and intracellular signal transduction networks. We have developed colloidal gold<br />
nanoparticles (GNPs) presenting a photocleavable succinimidyl ester that allows for the delivery<br />
of amine derivatives (Figure 1b). Under this molecular design, the GNPs capture the amine<br />
derivatives on their surfaces and release them upon irradiation at any desired time and space. As a<br />
proof of concept, we synthesized histamine-immobilized GNPs and examined their ability to<br />
evoke intracellular signaling by fluorescence imaging.<br />
(a) O<br />
(b)<br />
PEG NH2-PEG Non cell-adhesive Cell-adhesive<br />
Capture Release<br />
Figure 1. Photoresponsive Biointerfaces. (a) Change in cell adhesiveness on a photoactivatable cell culture substrate.<br />
(b) Capture and release of amine derivatives (NH2-R) on photoresponsive gold nanoparticles (GNPs).<br />
References:<br />
[1] J. Nakanishi et al. J. Am. Chem. Soc., 129, 6694, 2007; Y. Kikuchi et al. Chem. Lett., 37,<br />
1062, 2008.<br />
[2] J. Nakanishi et al. submitted.<br />
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Oral Presentation 14<br />
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