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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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