TY - JOUR
T1 - In vitro reconstitution of functional small ribosomal subunit assembly for comprehensive analysis of ribosomal elements in E. coli
AU - Shimojo, Masaru
AU - Amikura, Kazuaki
AU - Masuda, Keiko
AU - Kanamori, Takashi
AU - Ueda, Takuya
AU - Shimizu, Yoshihiro
N1 - Funding Information:
The authors thank Nono Takeuchi-Tomita for helpful discussions. This work was supported by a scholarship from The Futaba Foundation (to M.S.), a Grant-in-Aid in number 17H05680 (to Y.S.) and 15K16083 (to K.A.) from Japan Society for the Promotion of Science (JSPS), Human Frontier Science Program (RGP0043/2017 to Y.S.), Astrobiology Center Project of the National Institutes of Natural Sciences (AB271004 and AB281007 to K.A. and AB311005 to Y.S. and K.A.), and an intramural Grant-in-Aid from the RIKEN Center for Biosystems Dynamics Research (to Y.S.).
Publisher Copyright:
© 2020, The Author(s).
PY - 2020/12/1
Y1 - 2020/12/1
N2 - In vitro reconstitution is a powerful tool for investigating ribosome functions and biogenesis, as well as discovering new ribosomal features. In this study, we integrated all of the processes required for Escherichia coli small ribosomal subunit assembly. In our method, termed fully Recombinant-based integrated Synthesis, Assembly, and Translation (R-iSAT), assembly and evaluation of the small ribosomal subunits are coupled with ribosomal RNA (rRNA) synthesis in a reconstituted cell-free protein synthesis system. By changing the components of R-iSAT, including recombinant ribosomal protein composition, we coupled ribosomal assembly with ribosomal protein synthesis, enabling functional synthesis of ribosomal proteins and subsequent subunit assembly. In addition, we assembled and evaluated subunits with mutations in both rRNA and ribosomal proteins. The study demonstrated that our scheme provides new ways to comprehensively analyze any elements of the small ribosomal subunit, with the goal of improving our understanding of ribosomal biogenesis, function, and engineering.
AB - In vitro reconstitution is a powerful tool for investigating ribosome functions and biogenesis, as well as discovering new ribosomal features. In this study, we integrated all of the processes required for Escherichia coli small ribosomal subunit assembly. In our method, termed fully Recombinant-based integrated Synthesis, Assembly, and Translation (R-iSAT), assembly and evaluation of the small ribosomal subunits are coupled with ribosomal RNA (rRNA) synthesis in a reconstituted cell-free protein synthesis system. By changing the components of R-iSAT, including recombinant ribosomal protein composition, we coupled ribosomal assembly with ribosomal protein synthesis, enabling functional synthesis of ribosomal proteins and subsequent subunit assembly. In addition, we assembled and evaluated subunits with mutations in both rRNA and ribosomal proteins. The study demonstrated that our scheme provides new ways to comprehensively analyze any elements of the small ribosomal subunit, with the goal of improving our understanding of ribosomal biogenesis, function, and engineering.
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U2 - 10.1038/s42003-020-0874-8
DO - 10.1038/s42003-020-0874-8
M3 - Article
C2 - 32214223
AN - SCOPUS:85082569772
SN - 2399-3642
VL - 3
JO - Communications Biology
JF - Communications Biology
IS - 1
M1 - 142
ER -