具有 DSE 基调的微生物荷尔蒙蛋白的生物物理特征。

Biophysics and Physicobiology Pub Date : 2023-03-08 eCollection Date: 2023-03-21 DOI:10.2142/biophysico.bppb-v20.s023
María Del Carmen Marín, Alexander L Jaffe, Patrick T West, Masae Konno, Jillian F Banfield, Keiichi Inoue
{"title":"具有 DSE 基调的微生物荷尔蒙蛋白的生物物理特征。","authors":"María Del Carmen Marín, Alexander L Jaffe, Patrick T West, Masae Konno, Jillian F Banfield, Keiichi Inoue","doi":"10.2142/biophysico.bppb-v20.s023","DOIUrl":null,"url":null,"abstract":"<p><p>Microbial rhodopsins are photoreceptive transmembrane proteins that transport ions or regulate other intracellular biological processes. Recent genomic and metagenomic analyses found many microbial rhodopsins with unique sequences distinct from known ones. Functional characterization of these new types of microbial rhodopsins is expected to expand our understanding of their physiological roles. Here, we found microbial rhodopsins having a DSE motif in the third transmembrane helix from members of the Actinobacteria. Although the expressed proteins exhibited blue-green light absorption, either no or extremely small outward H<sup>+</sup> pump activity was observed. The turnover rate of the photocycle reaction of the purified proteins was extremely slow compared to typical H<sup>+</sup> pumps, suggesting these rhodopsins would work as photosensors or H<sup>+</sup> pumps whose activities are enhanced by an unknown regulatory system in the hosts. The discovery of this rhodopsin group with the unique motif and functionality expands our understanding of the biological role of microbial rhodopsins.</p>","PeriodicalId":8976,"journal":{"name":"Biophysics and Physicobiology","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2023-03-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10865882/pdf/","citationCount":"0","resultStr":"{\"title\":\"Biophysical characterization of microbial rhodopsins with DSE motif.\",\"authors\":\"María Del Carmen Marín, Alexander L Jaffe, Patrick T West, Masae Konno, Jillian F Banfield, Keiichi Inoue\",\"doi\":\"10.2142/biophysico.bppb-v20.s023\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Microbial rhodopsins are photoreceptive transmembrane proteins that transport ions or regulate other intracellular biological processes. Recent genomic and metagenomic analyses found many microbial rhodopsins with unique sequences distinct from known ones. Functional characterization of these new types of microbial rhodopsins is expected to expand our understanding of their physiological roles. Here, we found microbial rhodopsins having a DSE motif in the third transmembrane helix from members of the Actinobacteria. Although the expressed proteins exhibited blue-green light absorption, either no or extremely small outward H<sup>+</sup> pump activity was observed. The turnover rate of the photocycle reaction of the purified proteins was extremely slow compared to typical H<sup>+</sup> pumps, suggesting these rhodopsins would work as photosensors or H<sup>+</sup> pumps whose activities are enhanced by an unknown regulatory system in the hosts. The discovery of this rhodopsin group with the unique motif and functionality expands our understanding of the biological role of microbial rhodopsins.</p>\",\"PeriodicalId\":8976,\"journal\":{\"name\":\"Biophysics and Physicobiology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-03-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10865882/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Biophysics and Physicobiology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2142/biophysico.bppb-v20.s023\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2023/3/21 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biophysics and Physicobiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2142/biophysico.bppb-v20.s023","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/3/21 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

微生物菱形蛋白是一种感光跨膜蛋白,可运输离子或调节其他细胞内生物过程。最近的基因组学和元基因组学分析发现了许多具有不同于已知的独特序列的微生物菱形蛋白。对这些新型微生物荷尔蒙蛋白进行功能表征有望扩大我们对其生理作用的了解。在这里,我们从放线菌中发现了在第三跨膜螺旋中具有 DSE 基序的微生物犀角蛋白。虽然表达的蛋白质具有蓝绿光吸收功能,但没有观察到或观察到极小的外向 H+ 泵活性。与典型的 H+ 泵相比,纯化蛋白的光周期反应周转率极慢,这表明这些斜视蛋白可作为光敏元件或 H+ 泵工作,其活性可通过宿主体内的未知调节系统得到增强。这种具有独特图案和功能的犀牛蛋白群的发现,拓展了我们对微生物犀牛蛋白生物学作用的认识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Biophysical characterization of microbial rhodopsins with DSE motif.

Microbial rhodopsins are photoreceptive transmembrane proteins that transport ions or regulate other intracellular biological processes. Recent genomic and metagenomic analyses found many microbial rhodopsins with unique sequences distinct from known ones. Functional characterization of these new types of microbial rhodopsins is expected to expand our understanding of their physiological roles. Here, we found microbial rhodopsins having a DSE motif in the third transmembrane helix from members of the Actinobacteria. Although the expressed proteins exhibited blue-green light absorption, either no or extremely small outward H+ pump activity was observed. The turnover rate of the photocycle reaction of the purified proteins was extremely slow compared to typical H+ pumps, suggesting these rhodopsins would work as photosensors or H+ pumps whose activities are enhanced by an unknown regulatory system in the hosts. The discovery of this rhodopsin group with the unique motif and functionality expands our understanding of the biological role of microbial rhodopsins.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
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:481959085
Book学术官方微信