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-Size controllable Linear Homomultimer-TeamSendai2015

In nature, various biological functions are realized by multimeric proteins. In most cases, these proteins have intrinsic curvature and the number of monomers are determined by their circular assembly. However, in linear assembly, it is difficult to control the number of proteins without additional capping mechanisms. Here, we propose a novel mechanism to control the linear assembly by using a kind of vernier mechanism.

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-Size controllable Linear Homomultimer-TeamSendai2015 | teamsendai.github.io Reviews
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In nature, various biological functions are realized by multimeric proteins. In most cases, these proteins have intrinsic curvature and the number of monomers are determined by their circular assembly. However, in linear assembly, it is difficult to control the number of proteins without additional capping mechanisms. Here, we propose a novel mechanism to control the linear assembly by using a kind of vernier mechanism.
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3 simulation
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6 material and method
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-Size controllable Linear Homomultimer-TeamSendai2015 | teamsendai.github.io Reviews

https://teamsendai.github.io

In nature, various biological functions are realized by multimeric proteins. In most cases, these proteins have intrinsic curvature and the number of monomers are determined by their circular assembly. However, in linear assembly, it is difficult to control the number of proteins without additional capping mechanisms. Here, we propose a novel mechanism to control the linear assembly by using a kind of vernier mechanism.

LINKS TO THIS WEBSITE

molbot.mech.tohoku.ac.jp molbot.mech.tohoku.ac.jp

東北大学大学院工学研究科 バイオロボティクス専攻分子ロボティクス分野 村田・川又/野村研究室 Molecular Robotics Laboratory

http://www.molbot.mech.tohoku.ac.jp/index.html

東北大学大学院工学研究科 バイオロボティクス専攻分子ロボティクス分野 村田 川又 野村研究室 Molecular Robotics Laboratory. 分子ロボティクス は,情報科学,制御工学,機械工学,生物物理,化学などの多くの分野の境界領域に誕生しつつある新しい学問領域です 20世紀後半からの分子生物学の進展により,分子の機械としての生物のしくみの詳細がつぎつぎと明らかになっています 最近では,その知見を工学的に応用することにより,核酸やタンパク質などの生体分子を素材として,従来は考えられなかったような複雑な分子デバイスを製作することが可能になってきています 個々の分子デバイスをつくるだけでなく,たくさんの分子デバイスを統合し,より高度な機能をもつ分子の システム を構築するのが 分子ロボティクス です 分子機械の設計論をデバイスレベルからシステムレベルに飛躍させ,ナノメートル領域 ボトムアップな分子設計 とマイクロメートル領域 トップダウンの機械技術 MEMS の間の橋渡しをするのが分子ロボティクスであるとも言えるでしょう. BIOMOD2015 Team Sendai Wiki.

molbot.mech.tohoku.ac.jp molbot.mech.tohoku.ac.jp

BIOMOD:村田・川又/野村研究室 東北大学大学院工学研究科 バイオロボティクス専攻分子ロボティクス分野  Molecular Robotics Laboratory

http://www.molbot.mech.tohoku.ac.jp/biomod.html

東北大学大学院工学研究科 バイオロボティクス専攻分子ロボティクス分野 村田 川又 野村研究室 Molecular Robotics Laboratory.

biomod.net biomod.net

BIOMOD | Teams

http://biomod.net/teams

Location of and links to all the teams who participated in the Biomod Jamboree in 2015. In a larger map. Berlin Institute of Technology Team Berlin15. Indian Institute of Technology Kanpur Team Bioluminati. Hokkaido University BIOMOD Hokkaido. Huazhong University of Science and Technology Team HUST-China. UANL Universidad Autónoma de Nuevo León Team ImaGene. Jilin University Team Jilin-China. Shandong University Team Mount Tai. Ochanomizu University Team Ochadai. Rutgers University Team NZnzymes R Us.

biomod.net biomod.net

BIOMOD | BIOMOD 2015 Winners

http://biomod.net/winners

Grand Prize Total Combined Score. 1st: Team Sendai - Tohoku Univ. 2nd: NanocANDy - LMU. 3nd: HUST-China - Huazhong Univ of Sci&Tech. 5th Annual MOLBOT Award. Team Registration Opens Feb 15. Final Standings for BIOMOD 2015. See all blog entries ». Keep up with BIOMOD events and updates via our newsletter! Wyss Institute at Harvard University. 2014 President and Fellows of Harvard College. Designed by muckypaw.

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-Size controllable Linear Homomultimer-TeamSendai2015

In nature, various biological functions are realized by multimeric proteins. In most cases, these proteins have intrinsic curvature and the number of monomers are determined by their circular assembly. However, in linear assembly, it is difficult to control the number of proteins without additional capping mechanisms. Here, we propose a novel mechanism to control the linear assembly by using a kind of vernier mechanism.

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In this summer, we have designed two types of chemical reaction for the device and analyzed the behaviors of them both in vitro. Results of in vitro. Experiments demonstrate that our devices are able to release different single stranded DNA in proper order such as A-B, B-A, A-B-C, and C-A-B. The further properties such as output releasing intervals are predicted by in scilico.

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