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Updated: Jul 18, 2026

MS2-Affinity Purification Coupled with RNA Sequencing in Gram-Positive Bacteria
Published on: February 23, 2021
mRNA 3' of the A site bound codon is located close to protein S3 on the human 80S ribosome
Maxim V Molotkov1, Dmitri M Graifer, Elena A Popugaeva
1Institute of Chemical Biology and Fundamental Medicine, Novosibirsk, Russia
Abstract:
Ribosomal proteins neighboring the mRNA downstream of the codon bound at the decoding site of human 80S ribosomes were identified using three sets of mRNA analogues that contained a UUU triplet at the 5' terminus and a perfluorophenylazide cross-linker at guanosine, adenosine or uridine residues placed at various locations 3' of this triplet. The positions of modified mRNA nucleotides on the ribosome were governed by tRNA(Phe) cognate to the UUU triplet targeted to the P site. Upon mild UV-irradiation, the mRNA analogues cross-linked preferentially to the 40S subunit, to the proteins and to a lesser extent to the 18S rRNA. Cross-linked nucleotides of 18S rRNA were identified previously. In the present study, it is shown that among the proteins the main target for cross-linking with all the mRNA analogues tested was protein S3 (homologous to prokaryotic S3, S3p); minor cross-linking to protein S2 (S5p) was also detected. Both proteins cross-linked to mRNA analogues in the ternary complexes as well as in the binary complexes (without tRNA). In the ternary complexes protein S15 (S19p) also cross-linked, the yield of the cross-link decreased significantly when the modified nucleotide moved from position +5 to position +12 with respect to the first nucleotide of the P site bound codon. In several ternary complexes minor cross-linking to protein S30 was likewise detected. The results of this study indicate that S3 is a key protein at the mRNA binding site neighboring mRNA downstream of the codon at the decoding site in the human ribosome.
Insights
Human ribosomes utilize protein S3 as a key component for binding messenger RNA (mRNA) downstream of the decoding site. This finding helps understand the structural organization of the ribosome during protein synthesis.
Area of Science:
- Molecular Biology
- Ribosome Biology
- Protein Synthesis
Background:
- The human 80S ribosome plays a crucial role in translating messenger RNA (mRNA) into proteins.
- Understanding the precise interactions between ribosomal proteins and mRNA is essential for elucidating translation mechanisms.
- Previous studies identified cross-linked nucleotides in 18S ribosomal RNA (rRNA).
Purpose of the Study:
- To identify ribosomal proteins that interact with mRNA downstream of the decoding site in human ribosomes.
- To investigate the role of specific ribosomal proteins in mRNA binding during translation.
Main Methods:
- Utilized modified mRNA analogues with a UUU triplet and a cross-linker at various positions.
- Cross-linking was induced by UV irradiation in the presence of tRNA(Phe) (ternary complexes) and without tRNA (binary complexes).
- Identified cross-linked proteins using mass spectrometry.
Main Results:
- Protein S3 was the primary target for cross-linking with mRNA analogues in both ternary and binary complexes.
- Minor cross-linking was observed for proteins S2 and S15, with S15 cross-linking efficiency decreasing with distance from the P-site codon.
- Protein S30 showed minor cross-linking in several ternary complexes.
Conclusions:
- Protein S3 is a key protein involved in binding mRNA downstream of the decoding site on human ribosomes.
- These findings contribute to a deeper understanding of the human ribosome's mRNA binding site architecture and function.
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