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日時:平成27年1月14日(水) 午後3時~ 場所:蛋白質研究所 4階セミナー室 演者:横山 和重 先生 (ニューヨーク州立大学 ジェネセオ校 化学科) 世話人:大阪大学 蛋白質研究所 蛋白質構造形成研究室 後藤 祐児 睦月セミナー Controlling a Reversible Self-Assembly Path by Nanoscale Metal Surface 蛋白の 凝集調べて宇津之山 金銀粒子で岡部を超える Abstract Self-assembly of amyloid beta peptide (A) is a crucial step of the fibrillogenesis, which is considered as an onset hallmark mechanism of Alzheimer’s disease. We have succeeded to reproduce an oligomer formation of A 1-40 monomers over the nanogold colloidal surface as an external pH was changed between pH 4 and pH 10. Under pH 4, unfolded A 1-40 monomer constructed a dimer or trimer based oligomeric form with hydrophobic segment placing outward. On the other hand, a conformation of A constructed under pH 10 consists of a folded monomer with hydrophilic segment folded inward avoiding the networking with residual colloidal particles. While amyloid beta was attached to both silver and gold surface, more polarizable silver surface was found to restrict the channel of unfolding process. There was specific size/temperature dependence in a reversible self-assembly. Over 20 nm gold colloid, a reversible assembly process of A 1-40 monomer was observed in the temperature range of 5 C and up to 65 C. When 30 nm or 40 nm gold colloids were used a reversible self-assembly was observed below 5 C. Most probable oligomer form constructed over 20 nm gold colloidal surface is dimer based unit and that over 30 or 40 nm gold colloidal surface is concluded to be a trimer based unit. However, self-assembly was not successfully reproduced under the rest of conditions. A significant enhancement of a reversible self-assembly was achieved when a surface environment of gold colloid was functionalized with dibenzyloxy disulfide. The highest effect was obtained when electron donating group was used in para-substitution. It implies that electron density was more concentrated to the bonding between disulfide group and gold surface resulting a weaker interaction between A monomers and a functionalized group. A weaker bonding enabled to cause a flexible structural change between folded and unfolded forms. 東海道53次 岡部宿 宇津之山

Controlling a Reversible Self-Assembly Path by …Controlling a Reversible Self-Assembly Path by Nanoscale Metal Surface 蛋白の 凝集調べて宇津之山 金銀粒子で岡部を超える

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Page 1: Controlling a Reversible Self-Assembly Path by …Controlling a Reversible Self-Assembly Path by Nanoscale Metal Surface 蛋白の 凝集調べて宇津之山 金銀粒子で岡部を超える

日時:平成27年1月14日(水) 午後3時~場所:蛋白質研究所 4階セミナー室演者:横山 和重 先生 (ニューヨーク州立大学 ジェネセオ校 化学科)

世話人:大阪大学蛋白質研究所蛋白質構造形成研究室 後藤祐児

睦月セミナーControlling a Reversible Self-Assembly

Path by Nanoscale Metal Surface

蛋白の凝集調べて宇津之山金銀粒子で岡部を超える

AbstractSelf-assembly of amyloid beta peptide (A) is a crucial step of the fibrillogenesis, which is considered as an onset hallmark mechanism ofAlzheimer’s disease. We have succeeded to reproduce an oligomer formation of A1-40 monomers over the nanogold colloidal surface as anexternal pH was changed between pH 4 and pH 10. Under pH 4, unfolded A1-40 monomer constructed a dimer or trimer based oligomeric formwith hydrophobic segment placing outward. On the other hand, a conformation of A constructed under pH 10 consists of a folded monomerwith hydrophilic segment folded inward avoiding the networking with residual colloidal particles. While amyloid beta was attached to both silverand gold surface, more polarizable silver surface was found to restrict the channel of unfolding process. There was specific size/temperaturedependence in a reversible self-assembly. Over 20 nm gold colloid, a reversible assembly process of A1-40 monomer was observed in thetemperature range of 5 C and up to 65 C. When 30 nm or 40 nm gold colloids were used a reversible self-assembly was observed below 5 C.Most probable oligomer form constructed over 20 nm gold colloidal surface is dimer based unit and that over 30 or 40 nm gold colloidal surfaceis concluded to be a trimer based unit. However, self-assembly was not successfully reproduced under the rest of conditions. A significantenhancement of a reversible self-assembly was achieved when a surface environment of gold colloid was functionalized with dibenzyloxydisulfide. The highest effect was obtained when electron donating group was used in para-substitution. It implies that electron density was moreconcentrated to the bonding between disulfide group and gold surface resulting a weaker interaction between A monomers and afunctionalized group. A weaker bonding enabled to cause a flexible structural change between folded and unfolded forms.

東海道53次 岡部宿 宇津之山