Bridging ribosomal synthesis to cell growth through the lens of kinetics

Understanding prokaryotic cell growth requires a multiscale modeling framework from the kinetics perspective. The detailed kinetics pathway of ribosomes exhibits features beyond the scope of the classical Hopfield kinetics model. The complexity of the molecular responses to various nutrient conditio...

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Main Authors: Le, Luan Quang, Zhu, Kaicheng., Su, Haibin
Other Authors: School of Materials Science and Engineering
Format: Article
Language:English
Published: 2023
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Online Access:https://hdl.handle.net/10356/170592
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1705922023-09-20T01:21:41Z Bridging ribosomal synthesis to cell growth through the lens of kinetics Le, Luan Quang Zhu, Kaicheng. Su, Haibin School of Materials Science and Engineering Engineering::Materials Protein Biosynthesis Ribosomal Proteins Understanding prokaryotic cell growth requires a multiscale modeling framework from the kinetics perspective. The detailed kinetics pathway of ribosomes exhibits features beyond the scope of the classical Hopfield kinetics model. The complexity of the molecular responses to various nutrient conditions poses additional challenge to elucidate the cell growth. Herein, a kinetics framework is developed to bridge ribosomal synthesis to cell growth. For the ribosomal synthesis kinetics, the competitive binding between cognate and near-cognate tRNAs for ribosomes can be modulated by Mg2+. This results in distinct patterns of the speed – accuracy relation comprising “trade-off” and “competition” regimes. Furthermore, the cell growth rate is optimized by varying the characteristics of ribosomal synthesis through cellular responses to different nutrient conditions. In this scenario, cellular responses to nutrient conditions manifest by two quadratic scaling relations: one for nutrient flux versus cell mass, the other for ribosomal number versus growth rate. Both are in quantitative agreement with experimental measurements. This work is supported in part by the Southern Marine Science and Engineering Guangdong Laboratory (Guangzhou) (SMSEGL20SC01) and HKUST grant (R9418). 2023-09-20T01:21:40Z 2023-09-20T01:21:40Z 2023 Journal Article Le, L. Q., Zhu, K. & Su, H. (2023). Bridging ribosomal synthesis to cell growth through the lens of kinetics. Biophysical Journal, 122(3), 544-553. https://dx.doi.org/10.1016/j.bpj.2022.12.028 0006-3495 https://hdl.handle.net/10356/170592 10.1016/j.bpj.2022.12.028 122 2-s2.0-85146580357 3 122 544 553 en Biophysical Journal © 2022 Biophysical Society. All rights reserved.
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Engineering::Materials
Protein Biosynthesis
Ribosomal Proteins
spellingShingle Engineering::Materials
Protein Biosynthesis
Ribosomal Proteins
Le, Luan Quang
Zhu, Kaicheng.
Su, Haibin
Bridging ribosomal synthesis to cell growth through the lens of kinetics
description Understanding prokaryotic cell growth requires a multiscale modeling framework from the kinetics perspective. The detailed kinetics pathway of ribosomes exhibits features beyond the scope of the classical Hopfield kinetics model. The complexity of the molecular responses to various nutrient conditions poses additional challenge to elucidate the cell growth. Herein, a kinetics framework is developed to bridge ribosomal synthesis to cell growth. For the ribosomal synthesis kinetics, the competitive binding between cognate and near-cognate tRNAs for ribosomes can be modulated by Mg2+. This results in distinct patterns of the speed – accuracy relation comprising “trade-off” and “competition” regimes. Furthermore, the cell growth rate is optimized by varying the characteristics of ribosomal synthesis through cellular responses to different nutrient conditions. In this scenario, cellular responses to nutrient conditions manifest by two quadratic scaling relations: one for nutrient flux versus cell mass, the other for ribosomal number versus growth rate. Both are in quantitative agreement with experimental measurements.
author2 School of Materials Science and Engineering
author_facet School of Materials Science and Engineering
Le, Luan Quang
Zhu, Kaicheng.
Su, Haibin
format Article
author Le, Luan Quang
Zhu, Kaicheng.
Su, Haibin
author_sort Le, Luan Quang
title Bridging ribosomal synthesis to cell growth through the lens of kinetics
title_short Bridging ribosomal synthesis to cell growth through the lens of kinetics
title_full Bridging ribosomal synthesis to cell growth through the lens of kinetics
title_fullStr Bridging ribosomal synthesis to cell growth through the lens of kinetics
title_full_unstemmed Bridging ribosomal synthesis to cell growth through the lens of kinetics
title_sort bridging ribosomal synthesis to cell growth through the lens of kinetics
publishDate 2023
url https://hdl.handle.net/10356/170592
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