Nanoscale elongating control of the self-assembled protein filament with the cysteine-introduced building blocks

被引:24
作者
Usui, Kengo [1 ,2 ,3 ]
Maki, Tei [2 ,4 ]
Ito, Fuyu [1 ,2 ,3 ]
Suenaga, Atsushi [5 ]
Kidoaki, Satoru [4 ]
Itoh, Masayoshi [1 ,3 ]
Taiji, Makoto [5 ]
Matsuda, Takehisa [6 ]
Hayashizaki, Yoshihide [1 ,3 ]
Suzuki, Harukazu [1 ,3 ]
机构
[1] RIKEN Genom Sci Ctr GSC, Lab Genome Explorat Res Grp, Tsurumi Ku, Yokohama, Kanagawa 2300045, Japan
[2] Japan Sci & Technol Agcy, CREST, Kawaguchi, Saitama 3320012, Japan
[3] RIKEN, Genome Sci Lab, Wako, Saitama 3510198, Japan
[4] Kyushu Univ, Div Biomol Chem, Fukuoka 8128581, Japan
[5] RIKEN Genom Sci Ctr, Computat & Expt Syst Biol Grp, Kanagawa 2300046, Japan
[6] Kanazawa Inst Technol, Genome Biotechnol Lab, Kanazawa, Ishikawa 9240838, Japan
关键词
self-assembly; nanofilament; protein design; molecular modeling; protein nanomaterial; ERBIN PDZ DOMAIN; STREPTAVIDIN; SPECIFICITY; SYMMETRY; CATENIN; SYSTEM;
D O I
10.1002/pro.106
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Self-assembly of artificially designed proteins is extremely desirable for nanomaterials. Here we show a novel strategy for the creation of self-assembling proteins, named "Nanolego.'' Nanolego consists of "structural elements'' of a structurally stable symmetrical homo-oligomeric protein and "binding elements,'' which are multiple heterointeraction proteins with relatively weak affinity. We have established two key technologies for Nanolego, a stabilization method and a method for terminating the self-assembly process. The stabilization method is mediated by disulfide bonds between Cysteine-residues incorporated into the binding elements, and the termination method uses "capping Nanolegos,'' in which some of the binding elements in the Nanolego are absent for the self-assembled ends. With these technologies, we successfully constructed timing-controlled and size-regulated filament-shape complexes via Nanolego self-assembly. The Nanolego concept and these technologies should pave the way for regulated nanoarchitecture using designed proteins.
引用
收藏
页码:960 / 969
页数:10
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