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pH-Responsive and selective protein adsorption on an amino acid-based zwitterionic polymer surface

Year: 2015

Journal: POLYMER CHEMISTRY, Vol. 6, p 7053-7059, 20170208

Authors: Fujii, Shota; Kido, Makoto; Sato, Masanao; Higaki, Yuji; Hirai, Tomoyasu; Ohta, Noboru; Kojio, Ken; Takahara, Atsushi

Organizations: Kyushu Univ, Grad Sch Engn, Nishi Ku, Fukuoka 8190395, Japan; Kyushu Univ, Inst Mat Chem & Engn, Nishi Ku, Fukuoka 8190395, Japan; Kyushu Univ, Int Inst Carbon Neutral Energy Res WPI I2CNER, Nishi Ku, Fukuoka 8190395, Japan; Japan Synchrotron Radiat Res Inst JASRI SPring 8, Sayo, Hyogo 6795198, Japan

The synergistic interactions between the alpha-amine and the carboxylic acid in an amino acid have recently been studied as bio-based zwitterions. Here, we report a new amphiphilic polymer containing glutamic acid grafted to the end of a dodecyl polymer side chain, which contains the alpha-amine and the gamma-carboxylic acid of the glutamic acid moiety. The polymer self-assembled into a multilayered structure in the thin film, and the glutamic acid moieties in the polymer side chains were exposed to the polymer film/water interface. Annealing the sample enhanced the formation of a well-oriented lamellar structure in the films. Due to the presence of the glutamic acid moieties at the interface, the surface charge was controllable by pH in buffer solutions, resulting in zwitterionic character at neutral pH. It has been widely accepted that zwitterionic surfaces can exhibit non-fouling for proteins. Interestingly enough, the polymer film showed charge-selective protein adsorption since the synergistic interaction between the alpha-amine and the gamma-carboxylic acid was weaker than conventional amino acid-based zwitterionic systems. This is due to the separated state of the functional groups by a three carbon spacer.