Non-canonical Binding Site for Bacterial Initiation Factor 3 on the Large Ribosomal Subunit

被引:15
|
作者
Goyal, Akanksha [1 ]
Belardinelli, Riccardo [1 ]
Rodnina, Marina V. [1 ]
机构
[1] Max Planck Inst Biophys Chem, Dept Phys Biochem, Fassberg 11, D-37077 Gottingen, Germany
来源
CELL REPORTS | 2017年 / 20卷 / 13期
关键词
MESSENGER-RNA TRANSLATION; ESCHERICHIA-COLI; PROTEIN-SYNTHESIS; FACTOR IF3; FACTOR-III; 30S; COMPLEX; FLUORESCENCE; MOVEMENTS; SELECTION;
D O I
10.1016/j.celrep.2017.09.012
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Canonical translation initiation in bacteria entails the assembly of the 30S initiation complex (IC), which binds the 50S subunit to form a 70S IC. IF3, a key initiation factor, is recruited to the 30S subunit at an early stage and is displaced from its primary binding site upon subunit joining. We employed four different FRET pairs to monitor IF3 relocation after 50S joining. IF3 moves away from the 30S subunit, IF1 and IF2, but can remain bound to the mature 70S IC. The secondary binding site is located on the 50S subunit in the vicinity of ribosomal protein L33. The interaction between IF3 and the 50S subunit is largely electrostatic with very high rates of IF3 binding and dissociation. The existence of the non-canonical binding site may help explain how IF3 participates in alternative initiation modes performed directly by the 70S ri-bosomes, such as initiation on leaderless mRNAs or re-initiation.
引用
收藏
页码:3113 / 3122
页数:10
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