A DNA origami-based device for investigating DNA bending proteins by transmission electron microscopy

被引:2
|
作者
Natarajan, Ashwin Karthick [1 ,2 ]
Ryssy, Joonas [1 ,3 ]
Kuzyk, Anton [1 ]
机构
[1] Aalto Univ, Sch Sci, Dept Neurosci & Biomed Engn, POB 12200, FI-00076 Aalto, Finland
[2] Helmholtz Assoc, Max Delbruck Ctr Mol Med, Struct Biol, Robert Rossle Str 10, Berlin, Germany
[3] KTH Royal Inst Technol, Dept Chem, Teknikringen 30, S-10044 Stockholm, Sweden
基金
芬兰科学院;
关键词
TATA-BINDING PROTEIN; CRYSTAL-STRUCTURE; STRUCTURAL BASIS; TBP; TRANSCRIPTION; BOX; COMPLEX; TFIIA; CONFORMATION; STABILITY;
D O I
10.1039/d2nr05366g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The DNA origami technique offers precise positioning of nanoscale objects with high accuracy. This has facilitated the development of DNA origami-based functional nanomechanical devices that enable the investigation of DNA-protein interactions at the single particle level. Herein, we used the DNA origami technique to fabricate a nanoscale device for studying DNA bending proteins. For a proof of concept, we used TATA-box binding protein (TBP) to evaluate our approach. Upon binding to the TATA box, TBP causes a bend to DNA of similar to 90 degrees. Our device translates this bending into an angular change that is readily observable with a conventional transmission electron microscope (TEM). Furthermore, we investigated the roles of transcription factor II A (TF(II)A) and transcription factor II B (TF(II)B). Our results indicate that TF(II)A introduces additional bending, whereas TF(II)B does not significantly alter the TBP-DNA structure. Our approach can be readily adopted to a wide range of DNA-bending proteins and will aid the development of DNA-origami-based devices tailored for the investigation of DNA-protein interactions.
引用
收藏
页码:3212 / 3218
页数:7
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