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了解细胞中血红素的分布物流。

Understanding the Logistics for the Distribution of Heme in Cells.

作者信息

Gallio Andrea E, Fung Simon S-P, Cammack-Najera Ana, Hudson Andrew J, Raven Emma L

机构信息

School of Chemistry, University of Bristol, Cantock's Close, Bristol BS8 1TS, U.K.

Department of Chemistry and Leicester Institute of Structural and Chemical Biology, University of Leicester, Leicester LE1 7RH, U.K.

出版信息

JACS Au. 2021 Aug 10;1(10):1541-1555. doi: 10.1021/jacsau.1c00288. eCollection 2021 Oct 25.

DOI:10.1021/jacsau.1c00288
PMID:34723258
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8549057/
Abstract

Heme is essential for the survival of virtually all living systems-from bacteria, fungi, and yeast, through plants to animals. No eukaryote has been identified that can survive without heme. There are thousands of different proteins that require heme in order to function properly, and these are responsible for processes such as oxygen transport, electron transfer, oxidative stress response, respiration, and catalysis. Further to this, in the past few years, heme has been shown to have an important regulatory role in cells, in processes such as transcription, regulation of the circadian clock, and the gating of ion channels. To act in a regulatory capacity, heme needs to move from its place of synthesis (in mitochondria) to other locations in cells. But while there is detailed information on how the heme lifecycle begins (heme synthesis), and how it ends (heme degradation), what happens in between is largely a mystery. Here we summarize recent information on the quantification of heme in cells, and we present a discussion of a mechanistic framework that could meet the logistical challenge of heme distribution.

摘要

血红素对于几乎所有生命系统的生存都至关重要——从细菌、真菌、酵母到植物,再到动物。尚未发现任何真核生物能够在没有血红素的情况下存活。有成千上万种不同的蛋白质需要血红素才能正常发挥功能,这些蛋白质负责氧气运输、电子传递、氧化应激反应、呼吸作用和催化作用等过程。此外,在过去几年中,血红素已被证明在细胞中具有重要的调节作用,例如在转录、生物钟调节和离子通道门控等过程中。为了发挥调节作用,血红素需要从其合成位置(线粒体)转移到细胞中的其他位置。但是,虽然关于血红素生命周期如何开始(血红素合成)以及如何结束(血红素降解)有详细信息,但其间发生的事情在很大程度上仍是个谜。在这里,我们总结了细胞中血红素定量的最新信息,并讨论了一个能够应对血红素分布后勤挑战的机制框架。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec86/8549057/af2bc5232e88/au1c00288_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec86/8549057/0e68917ad3cb/au1c00288_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec86/8549057/86ce45ce5442/au1c00288_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec86/8549057/9e8ca04a10ea/au1c00288_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec86/8549057/95b346a0fabf/au1c00288_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec86/8549057/af2bc5232e88/au1c00288_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec86/8549057/0e68917ad3cb/au1c00288_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec86/8549057/86ce45ce5442/au1c00288_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec86/8549057/9e8ca04a10ea/au1c00288_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec86/8549057/95b346a0fabf/au1c00288_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec86/8549057/af2bc5232e88/au1c00288_0005.jpg

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Sci Transl Med. 2021 May 19;13(594). doi: 10.1126/scitranslmed.abd1869.
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Heme Detoxification in the Malaria Parasite: A Target for Antimalarial Drug Development.疟原虫血红素解毒:抗疟药物研发的新靶点
生化图谱揭示了在I型细菌细胞色素生物合成中通过CcmCD的保守血红素转运机制。
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Heme regulates protein interactions and phosphorylation of BACH2 intrinsically disordered region in humoral response.血红素在体液免疫反应中调节蛋白质相互作用以及BACH2内在无序区域的磷酸化。
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Discovery and binding mode of small molecule inhibitors of the apo form of human TDO2.人源脱羧酶 TDO2 无酶形式的小分子抑制剂的发现及结合模式。
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