Rapid Adaptation of Cyanobacteria to Environmental Perturbations Is Achieved Through Structural Remodeling of the Proteome.

IF 6.3 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Molecular & Cellular Proteomics Pub Date : 2026-07-01 Epub Date: 2025-11-03 DOI:10.1016/j.mcpro.2025.101443
Snigdha Sarkar, Elise M Van Fossen, Xiaolu Li, Tong Zhang, Song Feng, Victoria Prozapas, Ivo Díaz Ludovico, Abdullah D Shouaib, Chelsea M Hutchinson-Bunch, Natalie C Sadler, Isaac K Attah, Wei-Jun Qian, Margaret S Cheung, Pavlo Bohutskyi, John T Melchior
{"title":"Rapid Adaptation of Cyanobacteria to Environmental Perturbations Is Achieved Through Structural Remodeling of the Proteome.","authors":"Snigdha Sarkar, Elise M Van Fossen, Xiaolu Li, Tong Zhang, Song Feng, Victoria Prozapas, Ivo Díaz Ludovico, Abdullah D Shouaib, Chelsea M Hutchinson-Bunch, Natalie C Sadler, Isaac K Attah, Wei-Jun Qian, Margaret S Cheung, Pavlo Bohutskyi, John T Melchior","doi":"10.1016/j.mcpro.2025.101443","DOIUrl":null,"url":null,"abstract":"<p><p>Dynamic environments require cyanobacteria to rapidly respond to fluctuating light conditions on timescales faster than transcription-translation processes allow, which is possible through immediate regulation of protein function via molecular and conformational adjustments. Traditional abundance-based proteomics cannot capture these rapid structural changes, creating a critical gap in understanding cellular adaptation mechanisms. We hypothesized that application of alternative structural proteomics approaches would enable identification of immediate structural remodeling across the cyanobacterial proteome triggered by environmental perturbations, potentially driving functional adaptations invisible to conventional abundance-based methods. We interrogated three complementary techniques-limited proteolysis-based mass spectrometry, thermal proteome profiling, and redox proteomics-for their capacity to unveil structural reorganization within the model cyanobacterium Synechococcus elongatus PCC 7942 during physiologically relevant light transitions. Within 30 min of increased light exposure, we detected structural changes in 753 proteins (limited proteolysis-based mass spectrometry), thermal stability shifts in 600 proteins (thermal proteome profiling), and cysteine oxidation in 1887 sites, while only 145 proteins changed in abundance. All three techniques consistently revealed coordinated remodeling of photosynthetic machinery, ribosomal complexes, and carbon metabolism, exemplified by cytochrome f stabilization modulating electron transport efficiency. Remarkably, <10% of proteins overlapped between methods, demonstrating that each technique captures distinct molecular dimensions of environmental adaptation. This structural proteomics framework demonstrates how alternative techniques can reveal hidden facets of proteome dynamics underlying cellular processes, offering new methodological approaches for understanding environmental responses and informing biotechnological applications.</p>","PeriodicalId":18712,"journal":{"name":"Molecular & Cellular Proteomics","volume":" ","pages":"101443"},"PeriodicalIF":6.3000,"publicationDate":"2026-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13424402/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular & Cellular Proteomics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.mcpro.2025.101443","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/11/3 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0

Abstract

Dynamic environments require cyanobacteria to rapidly respond to fluctuating light conditions on timescales faster than transcription-translation processes allow, which is possible through immediate regulation of protein function via molecular and conformational adjustments. Traditional abundance-based proteomics cannot capture these rapid structural changes, creating a critical gap in understanding cellular adaptation mechanisms. We hypothesized that application of alternative structural proteomics approaches would enable identification of immediate structural remodeling across the cyanobacterial proteome triggered by environmental perturbations, potentially driving functional adaptations invisible to conventional abundance-based methods. We interrogated three complementary techniques-limited proteolysis-based mass spectrometry, thermal proteome profiling, and redox proteomics-for their capacity to unveil structural reorganization within the model cyanobacterium Synechococcus elongatus PCC 7942 during physiologically relevant light transitions. Within 30 min of increased light exposure, we detected structural changes in 753 proteins (limited proteolysis-based mass spectrometry), thermal stability shifts in 600 proteins (thermal proteome profiling), and cysteine oxidation in 1887 sites, while only 145 proteins changed in abundance. All three techniques consistently revealed coordinated remodeling of photosynthetic machinery, ribosomal complexes, and carbon metabolism, exemplified by cytochrome f stabilization modulating electron transport efficiency. Remarkably, <10% of proteins overlapped between methods, demonstrating that each technique captures distinct molecular dimensions of environmental adaptation. This structural proteomics framework demonstrates how alternative techniques can reveal hidden facets of proteome dynamics underlying cellular processes, offering new methodological approaches for understanding environmental responses and informing biotechnological applications.

蓝藻对环境扰动的快速适应是通过蛋白质组的结构重塑实现的。
动态环境要求蓝藻在时间尺度上快速响应波动的光条件,比转录-翻译过程允许的更快,这可能通过分子和构象调整来立即调节蛋白质功能。传统的基于丰度的蛋白质组学不能捕捉到这些快速的结构变化,这在理解细胞适应机制方面造成了一个关键的空白。我们假设,应用替代结构蛋白质组学方法将能够识别由环境扰动触发的蓝藻蛋白质组的直接和广泛的结构重塑,潜在地推动传统的基于丰度的方法不可见的功能适应。我们研究了三种互补的技术——有限蛋白水解质谱(LiP-MS)、热蛋白质组谱(TPP-MS)和氧化还原蛋白质组学——以揭示蓝藻长聚球菌(Synechococcus elongatus) PCC 7942在生理相关光转换过程中的结构重组能力。在增加光照的30分钟内,我们检测到753个蛋白质的结构变化(LiP-MS), 600个蛋白质的热稳定性变化(TPP-MS), 1887个位点的半胱氨酸氧化,而只有145个蛋白质的丰度发生了变化。这三种技术一致地揭示了光合机制、核糖体复合物和碳代谢的协调重建,例如细胞色素稳定调节电子传递效率。值得注意的是,
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Molecular & Cellular Proteomics
Molecular & Cellular Proteomics 生物-生化研究方法
CiteScore
11.50
自引率
4.30%
发文量
131
审稿时长
84 days
期刊介绍: The mission of MCP is to foster the development and applications of proteomics in both basic and translational research. MCP will publish manuscripts that report significant new biological or clinical discoveries underpinned by proteomic observations across all kingdoms of life. Manuscripts must define the biological roles played by the proteins investigated or their mechanisms of action. The journal also emphasizes articles that describe innovative new computational methods and technological advancements that will enable future discoveries. Manuscripts describing such approaches do not have to include a solution to a biological problem, but must demonstrate that the technology works as described, is reproducible and is appropriate to uncover yet unknown protein/proteome function or properties using relevant model systems or publicly available data. Scope: -Fundamental studies in biology, including integrative "omics" studies, that provide mechanistic insights -Novel experimental and computational technologies -Proteogenomic data integration and analysis that enable greater understanding of physiology and disease processes -Pathway and network analyses of signaling that focus on the roles of post-translational modifications -Studies of proteome dynamics and quality controls, and their roles in disease -Studies of evolutionary processes effecting proteome dynamics, quality and regulation -Chemical proteomics, including mechanisms of drug action -Proteomics of the immune system and antigen presentation/recognition -Microbiome proteomics, host-microbe and host-pathogen interactions, and their roles in health and disease -Clinical and translational studies of human diseases -Metabolomics to understand functional connections between genes, proteins and phenotypes
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书