隐花色素4b蛋白可能与欧洲知更鸟基于自由基对的磁接受无关。

IF 3.5 2区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
Journal of The Royal Society Interface Pub Date : 2025-08-01 Epub Date: 2025-08-20 DOI:10.1098/rsif.2025.0176
Jingjing Xu, Alisha Bhanu Pattani Ameerjan, Jonathan Hungerland, Georg Langebrake, Tina Ravnsborg, Ole N Jensen, Jessica Schmidt, Rabea Bartölke, Takaoki Kasahara, Baladev Satish, Leonard Schwigon, Karin Dedek, Arne W Nolte, Miriam Liedvogel, Ilia A Solovyov, Henrik Mouritsen
{"title":"隐花色素4b蛋白可能与欧洲知更鸟基于自由基对的磁接受无关。","authors":"Jingjing Xu, Alisha Bhanu Pattani Ameerjan, Jonathan Hungerland, Georg Langebrake, Tina Ravnsborg, Ole N Jensen, Jessica Schmidt, Rabea Bartölke, Takaoki Kasahara, Baladev Satish, Leonard Schwigon, Karin Dedek, Arne W Nolte, Miriam Liedvogel, Ilia A Solovyov, Henrik Mouritsen","doi":"10.1098/rsif.2025.0176","DOIUrl":null,"url":null,"abstract":"<p><p>Avian cryptochrome 4 (Cry4) protein is a putative magnetosensitive molecule facilitating precise long-distance navigation in migratory birds. Two splice variants of Cry4 have been reported in the European robin (<i>Erithacus rubecula</i>), namely <i>Er</i>Cry4a and <i>Er</i>Cry4b. <i>Er</i>Cry4a protein is known to generate magnetically sensitive radical pairs for magnetoreception through electron transfer between the flavin adenine dinucleotide (FAD) cofactor and tryptophan residues within the protein. However, little is known about the <i>Er</i>Cry4b isoform. We therefore characterize the properties of <i>Er</i>Cry4b to determine whether it fulfils the prerequisites to be a radical-pair magnetic sensor molecule. Our results show that <i>Er</i>Cry4b protein does not bind FAD <i>in vitro</i>. Computational simulations reveal that the lack of FAD binding in <i>Er</i>Cry4b is probably due to protein structural dynamics. Furthermore, immunoprecipitation assays coupled with mass spectrometry suggest that <i>Er</i>Cry4b protein is undetectable in the robin retina, cerebellum, and liver. Meanwhile, transcript analyses show that <i>ErCRY4b</i> mRNA abundance is 10 times lower than that of <i>ErCRY4a</i> in the retina. In conclusion, <i>Er</i>Cry4b does not fulfil the prerequisites to be a radical pair-based magnetic sensing molecule due to the lack of FAD binding, and it might not even be expressed as a functional protein in the European robin.</p>","PeriodicalId":17488,"journal":{"name":"Journal of The Royal Society Interface","volume":"22 229","pages":"20250176"},"PeriodicalIF":3.5000,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12364574/pdf/","citationCount":"0","resultStr":"{\"title\":\"Cryptochrome 4b protein is probably irrelevant for radical pair-based magnetoreception in the European robin.\",\"authors\":\"Jingjing Xu, Alisha Bhanu Pattani Ameerjan, Jonathan Hungerland, Georg Langebrake, Tina Ravnsborg, Ole N Jensen, Jessica Schmidt, Rabea Bartölke, Takaoki Kasahara, Baladev Satish, Leonard Schwigon, Karin Dedek, Arne W Nolte, Miriam Liedvogel, Ilia A Solovyov, Henrik Mouritsen\",\"doi\":\"10.1098/rsif.2025.0176\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Avian cryptochrome 4 (Cry4) protein is a putative magnetosensitive molecule facilitating precise long-distance navigation in migratory birds. Two splice variants of Cry4 have been reported in the European robin (<i>Erithacus rubecula</i>), namely <i>Er</i>Cry4a and <i>Er</i>Cry4b. <i>Er</i>Cry4a protein is known to generate magnetically sensitive radical pairs for magnetoreception through electron transfer between the flavin adenine dinucleotide (FAD) cofactor and tryptophan residues within the protein. However, little is known about the <i>Er</i>Cry4b isoform. We therefore characterize the properties of <i>Er</i>Cry4b to determine whether it fulfils the prerequisites to be a radical-pair magnetic sensor molecule. Our results show that <i>Er</i>Cry4b protein does not bind FAD <i>in vitro</i>. Computational simulations reveal that the lack of FAD binding in <i>Er</i>Cry4b is probably due to protein structural dynamics. Furthermore, immunoprecipitation assays coupled with mass spectrometry suggest that <i>Er</i>Cry4b protein is undetectable in the robin retina, cerebellum, and liver. Meanwhile, transcript analyses show that <i>ErCRY4b</i> mRNA abundance is 10 times lower than that of <i>ErCRY4a</i> in the retina. In conclusion, <i>Er</i>Cry4b does not fulfil the prerequisites to be a radical pair-based magnetic sensing molecule due to the lack of FAD binding, and it might not even be expressed as a functional protein in the European robin.</p>\",\"PeriodicalId\":17488,\"journal\":{\"name\":\"Journal of The Royal Society Interface\",\"volume\":\"22 229\",\"pages\":\"20250176\"},\"PeriodicalIF\":3.5000,\"publicationDate\":\"2025-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12364574/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of The Royal Society Interface\",\"FirstCategoryId\":\"103\",\"ListUrlMain\":\"https://doi.org/10.1098/rsif.2025.0176\",\"RegionNum\":2,\"RegionCategory\":\"综合性期刊\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/8/20 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"MULTIDISCIPLINARY SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of The Royal Society Interface","FirstCategoryId":"103","ListUrlMain":"https://doi.org/10.1098/rsif.2025.0176","RegionNum":2,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/8/20 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
引用次数: 0

摘要

禽隐色素4 (Cry4)蛋白被认为是一种磁敏感分子,有助于候鸟进行精确的远距离导航。在欧洲知更鸟(Erithacus rubecula)中已经报道了Cry4的两个剪接变体,即ErCry4a和ErCry4b。已知ErCry4a蛋白通过黄素腺嘌呤二核苷酸(FAD)辅助因子和色氨酸残基之间的电子转移产生磁敏感自由基对进行磁接受。然而,人们对ErCry4b亚型知之甚少。因此,我们表征了ErCry4b的性质,以确定它是否满足成为自由基对磁传感器分子的先决条件。结果表明,ErCry4b蛋白在体外不与FAD结合。计算模拟表明,ErCry4b中缺乏FAD结合可能是由于蛋白质结构动力学。此外,免疫沉淀试验结合质谱分析表明,在知更鸟视网膜、小脑和肝脏中检测不到ErCry4b蛋白。同时,转录本分析显示,视网膜中ErCRY4b mRNA丰度比ErCRY4a低10倍。综上所述,由于缺乏FAD结合,ErCry4b不具备成为基于自由基对的磁传感分子的先决条件,甚至可能无法在欧洲知更鸟中作为功能性蛋白表达。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cryptochrome 4b protein is probably irrelevant for radical pair-based magnetoreception in the European robin.

Avian cryptochrome 4 (Cry4) protein is a putative magnetosensitive molecule facilitating precise long-distance navigation in migratory birds. Two splice variants of Cry4 have been reported in the European robin (Erithacus rubecula), namely ErCry4a and ErCry4b. ErCry4a protein is known to generate magnetically sensitive radical pairs for magnetoreception through electron transfer between the flavin adenine dinucleotide (FAD) cofactor and tryptophan residues within the protein. However, little is known about the ErCry4b isoform. We therefore characterize the properties of ErCry4b to determine whether it fulfils the prerequisites to be a radical-pair magnetic sensor molecule. Our results show that ErCry4b protein does not bind FAD in vitro. Computational simulations reveal that the lack of FAD binding in ErCry4b is probably due to protein structural dynamics. Furthermore, immunoprecipitation assays coupled with mass spectrometry suggest that ErCry4b protein is undetectable in the robin retina, cerebellum, and liver. Meanwhile, transcript analyses show that ErCRY4b mRNA abundance is 10 times lower than that of ErCRY4a in the retina. In conclusion, ErCry4b does not fulfil the prerequisites to be a radical pair-based magnetic sensing molecule due to the lack of FAD binding, and it might not even be expressed as a functional protein in the European robin.

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
Journal of The Royal Society Interface
Journal of The Royal Society Interface 综合性期刊-综合性期刊
CiteScore
7.10
自引率
2.60%
发文量
234
审稿时长
2.5 months
期刊介绍: J. R. Soc. Interface welcomes articles of high quality research at the interface of the physical and life sciences. It provides a high-quality forum to publish rapidly and interact across this boundary in two main ways: J. R. Soc. Interface publishes research applying chemistry, engineering, materials science, mathematics and physics to the biological and medical sciences; it also highlights discoveries in the life sciences of relevance to the physical sciences. Both sides of the interface are considered equally and it is one of the only journals to cover this exciting new territory. J. R. Soc. Interface welcomes contributions on a diverse range of topics, including but not limited to; biocomplexity, bioengineering, bioinformatics, biomaterials, biomechanics, bionanoscience, biophysics, chemical biology, computer science (as applied to the life sciences), medical physics, synthetic biology, systems biology, theoretical biology and tissue engineering.
×
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