Identification of RNAIII-binding proteins in Staphylococcus aureus using tethered RNAs and streptavidin aptamers based pull-down assay
BMC Microbiology, ISSN: 1471-2180, Vol: 15, Issue: 1, Page: 102-null
2015
- 8Citations
- 45Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations8
- Citation Indexes8
- CrossRef6
- Captures45
- Readers45
- 45
Article Description
Background: It has been widely recognized that small RNAs (sRNAs) play important roles in physiology and virulence control in bacteria. In Staphylococcus aureus, many sRNAs have been identified and some of them have been functionally studied. Since it is difficult to identify RNA-binding proteins (RBPs), very little has been known about the RBPs in S. aureus, especially those associated with sRNAs. Results: Here we adopted a tRNA scaffold streptavidin aptamer based pull-down assay to identify RBPs in S. aureus. The tethered RNA was successfully captured by the streptavidin magnetic beads, and proteins binding to RNAIII were isolated and analyzed by mass spectrometry. We have identified 81 proteins, and expressed heterologously 9 of them in Escherichia coli. The binding ability of the recombinant proteins with RNAIII was further analyzed by electrophoresis mobility shift assay, and the result indicates that proteins CshA, RNase J2, Era, Hu, WalR, Pyk, and FtsZ can bind to RNAIII. Conclusions: This study suggests that some proteins can bind to RNA III in S. aureus, and may be involved in RNA III function. And tRSA based pull-down assay is an effective method to search for RBPs in bacteria, which should facilitate the identification and functional study of RBPs in diverse bacterial species.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85018111936&origin=inward; http://dx.doi.org/10.1186/s12866-015-0435-3; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84938985519&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/25976342; https://bmcmicrobiol.biomedcentral.com/articles/10.1186/s12866-015-0435-3; https://dx.doi.org/10.1186/s12866-015-0435-3; http://www.biomedcentral.com/1471-2180/15/102; https://bmcmicrobiol.biomedcentral.com/counter/pdf/10.1186/s12866-015-0435-3; http://bmcmicrobiol.biomedcentral.com/articles/10.1186/s12866-015-0435-3
Springer Science and Business Media LLC
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