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Structural Insights into the FtsQ/FtsB/FtsL Complex, a Key Component of the Divisome
Bacterial cell division is a fundamental process that results in the physical separation of a mother cell into two daughter cells and involves a set of proteins known as the divisome. Among them, the FtsQ/FtsB/FtsL complex was known as a scaffold protein complex, but its overall structure and exact...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305486/ https://www.ncbi.nlm.nih.gov/pubmed/30584256 http://dx.doi.org/10.1038/s41598-018-36001-2 |
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author | Choi, Yuri Kim, Jinwoo Yoon, Hye-Jin Jin, Kyeong Sik Ryu, Sangryeol Lee, Hyung Ho |
author_facet | Choi, Yuri Kim, Jinwoo Yoon, Hye-Jin Jin, Kyeong Sik Ryu, Sangryeol Lee, Hyung Ho |
author_sort | Choi, Yuri |
collection | PubMed |
description | Bacterial cell division is a fundamental process that results in the physical separation of a mother cell into two daughter cells and involves a set of proteins known as the divisome. Among them, the FtsQ/FtsB/FtsL complex was known as a scaffold protein complex, but its overall structure and exact function is not precisely known. In this study, we have determined the crystal structure of the periplasmic domain of FtsQ in complex with the C-terminal fragment of FtsB, and showed that the C-terminal region of FtsB is a key binding region of FtsQ via mutational analysis in vitro and in vivo. We also obtained the solution structure of the periplasmic FtsQ/FtsB/FtsL complex by small angle X-ray scattering (SAXS), which reveals its structural organization. Interestingly, the SAXS and analytical gel filtration data showed that the FtsQ/FtsB/FtsL complex forms a 2:2:2 heterohexameric assembly in solution with the “Y” shape. Based on the model, the N-terminal directions of FtsQ and the FtsB/FtsL complex should be opposite, suggesting that the Y-shaped FtsQ/FtsB/FtsL complex might fit well into the curved membrane for membrane anchoring. |
format | Online Article Text |
id | pubmed-6305486 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-63054862018-12-31 Structural Insights into the FtsQ/FtsB/FtsL Complex, a Key Component of the Divisome Choi, Yuri Kim, Jinwoo Yoon, Hye-Jin Jin, Kyeong Sik Ryu, Sangryeol Lee, Hyung Ho Sci Rep Article Bacterial cell division is a fundamental process that results in the physical separation of a mother cell into two daughter cells and involves a set of proteins known as the divisome. Among them, the FtsQ/FtsB/FtsL complex was known as a scaffold protein complex, but its overall structure and exact function is not precisely known. In this study, we have determined the crystal structure of the periplasmic domain of FtsQ in complex with the C-terminal fragment of FtsB, and showed that the C-terminal region of FtsB is a key binding region of FtsQ via mutational analysis in vitro and in vivo. We also obtained the solution structure of the periplasmic FtsQ/FtsB/FtsL complex by small angle X-ray scattering (SAXS), which reveals its structural organization. Interestingly, the SAXS and analytical gel filtration data showed that the FtsQ/FtsB/FtsL complex forms a 2:2:2 heterohexameric assembly in solution with the “Y” shape. Based on the model, the N-terminal directions of FtsQ and the FtsB/FtsL complex should be opposite, suggesting that the Y-shaped FtsQ/FtsB/FtsL complex might fit well into the curved membrane for membrane anchoring. Nature Publishing Group UK 2018-12-24 /pmc/articles/PMC6305486/ /pubmed/30584256 http://dx.doi.org/10.1038/s41598-018-36001-2 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Choi, Yuri Kim, Jinwoo Yoon, Hye-Jin Jin, Kyeong Sik Ryu, Sangryeol Lee, Hyung Ho Structural Insights into the FtsQ/FtsB/FtsL Complex, a Key Component of the Divisome |
title | Structural Insights into the FtsQ/FtsB/FtsL Complex, a Key Component of the Divisome |
title_full | Structural Insights into the FtsQ/FtsB/FtsL Complex, a Key Component of the Divisome |
title_fullStr | Structural Insights into the FtsQ/FtsB/FtsL Complex, a Key Component of the Divisome |
title_full_unstemmed | Structural Insights into the FtsQ/FtsB/FtsL Complex, a Key Component of the Divisome |
title_short | Structural Insights into the FtsQ/FtsB/FtsL Complex, a Key Component of the Divisome |
title_sort | structural insights into the ftsq/ftsb/ftsl complex, a key component of the divisome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6305486/ https://www.ncbi.nlm.nih.gov/pubmed/30584256 http://dx.doi.org/10.1038/s41598-018-36001-2 |
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