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Photoinduced in situ formation of various F‐actin assemblies with a photoresponsive polycation
Author(s) -
Misu Manami,
Furukawa Hidemitsu,
Kwon HyuckJoon,
Shikinaka Kazuhiro,
Kakugo Akira,
Satoh Toshifumi,
Osada Yoshihito,
Gong Jian Ping
Publication year - 2009
Publication title -
journal of biomedical materials research part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.849
H-Index - 150
eISSN - 1552-4965
pISSN - 1549-3296
DOI - 10.1002/jbm.a.31990
Subject(s) - cationic polymerization , aqueous solution , monomer , materials science , in situ , photochemistry , actin , polymer chemistry , irradiation , molecule , biophysics , polymer , chemistry , organic chemistry , biochemistry , physics , nuclear physics , composite material , biology
We developed a novel in situ method for the control of F‐actin assembly by using a synthetic photoresponsive polycation. The photoresponsive polycation mainly comprises a water‐soluble cationic monomer and also contains a small amount of the monomer of a triphenylmethane leucohydroxide derivative (20 mol %), which is a well‐known photochromic molecule that can be cationized in aqueous solution by ultra violet (UV) irradiation, thereby causing an increase in the total charge on the photoresponsive polycation. Thus, by exposure to UV radiation in aqueous solution, F‐actin and the photoresponsive polycation start assembling into F‐actin/photoresponsive polycation complexes of various morphologies such as bundles, coils, and networks, depending upon the concentrations of both the F‐actin and salt. Further, localized UV irradiation can be applied in order to control the local formation of F‐actin/photoresponsive polycation complexes. Thus, this technique provides a novel method for the spatiotemporal control of F‐actin assembly and can be applied to investigate the unknown characteristics of F‐actin. © 2008 Wiley Periodicals, Inc. J Biomed Mater Res, 2009