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本文引用的文献

1
Commentary: MagR Alone Is Insufficient to Confer Cellular Calcium Responses to Magnetic Stimulation.评论:仅磁受体蛋白不足以赋予细胞对磁刺激产生钙反应。
Front Neural Circuits. 2018 Nov 12;12:97. doi: 10.3389/fncir.2018.00097. eCollection 2018.
2
Protein crystallization in living cells.活细胞中的蛋白质结晶。
Biol Chem. 2018 Jun 27;399(7):751-772. doi: 10.1515/hsz-2018-0158.
3
From bead to rod: Comparison of theories by measuring translational drag coefficients of micron-sized magnetic bead-chains in Stokes flow.从珠子到杆:通过测量斯托克斯流中微米级磁珠链的平移阻力系数比较理论
PLoS One. 2017 Nov 16;12(11):e0188015. doi: 10.1371/journal.pone.0188015. eCollection 2017.
4
Engineered Ferritin for Magnetogenetic Manipulation of Proteins and Organelles Inside Living Cells.工程化铁蛋白用于在活细胞内对蛋白质和细胞器进行磁遗传学操作。
Adv Mater. 2017 Nov;29(42). doi: 10.1002/adma.201700189. Epub 2017 Sep 28.
5
Magnetothermal genetic deep brain stimulation of motor behaviors in awake, freely moving mice.在清醒、自由活动的小鼠中进行磁热基因深脑刺激以调节运动行为。
Elife. 2017 Aug 15;6:e27069. doi: 10.7554/eLife.27069.
6
Buffers Strongly Modulate Fibrin Self-Assembly into Fibrous Networks.缓冲液强烈调节纤维蛋白原自组装成纤维网络。
Langmuir. 2017 Jun 27;33(25):6342-6352. doi: 10.1021/acs.langmuir.7b00527. Epub 2017 Jun 13.
7
Is magnetogenetics the new optogenetics?磁遗传学是新的光遗传学吗?
EMBO J. 2017 Jun 14;36(12):1643-1646. doi: 10.15252/embj.201797177. Epub 2017 May 23.
8
MagR Alone Is Insufficient to Confer Cellular Calcium Responses to Magnetic Stimulation.单独的MagR不足以赋予细胞对磁刺激的钙反应。
Front Neural Circuits. 2017 Mar 16;11:11. doi: 10.3389/fncir.2017.00011. eCollection 2017.
9
Widespread distribution of encapsulin nanocompartments reveals functional diversity.封装蛋白纳米容器的广泛分布揭示了功能多样性。
Nat Microbiol. 2017 Mar 6;2:17029. doi: 10.1038/nmicrobiol.2017.29.
10
Crystal Engineering of Self-Assembled Porous Protein Materials in Living Cells.活细胞中自组装多孔蛋白材料的晶体工程。
ACS Nano. 2017 Mar 28;11(3):2410-2419. doi: 10.1021/acsnano.6b06099. Epub 2017 Feb 9.

工程化遗传编码磁性蛋白晶体。

Engineering a Genetically Encoded Magnetic Protein Crystal.

机构信息

Department of Chemistry , Stanford University , Stanford , California 94305 , United States.

Department of Psychiatry and Behavioral Sciences , Stanford University , Stanford , California 94305 , United States.

出版信息

Nano Lett. 2019 Oct 9;19(10):6955-6963. doi: 10.1021/acs.nanolett.9b02266. Epub 2019 Sep 25.

DOI:10.1021/acs.nanolett.9b02266
PMID:31552740
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7265822/
Abstract

Magnetogenetics is a new field that leverages genetically encoded proteins and protein assemblies that are sensitive to magnetic fields to study and manipulate cell behavior. Theoretical studies show that many proposed magnetogenetic proteins do not contain enough iron to generate substantial magnetic forces. Here, we have engineered a genetically encoded ferritin-containing protein crystal that grows inside mammalian cells. Each of these crystals contains more than 10 million ferritin subunits and is capable of mineralizing substantial amounts of iron. When isolated from cells and loaded with iron , these crystals generate magnetic forces that are 9 orders of magnitude larger than the forces from the single ferritin cages used in previous studies. These protein crystals are attracted to an applied magnetic field and move toward magnets even when internalized into cells. While additional studies are needed to realize the full potential of magnetogenetics, these results demonstrate the feasibility of engineering protein assemblies for magnetic sensing.

摘要

磁遗传学是一个新兴领域,它利用对磁场敏感的基因编码蛋白和蛋白组装体来研究和操纵细胞行为。理论研究表明,许多提出的磁遗传学蛋白中并不含有足够的铁来产生实质性的磁场力。在这里,我们设计了一种基因编码的含铁蛋白晶体,它在哺乳动物细胞内生长。这些晶体中的每一个都含有超过 1000 万个铁蛋白亚基,能够矿化大量的铁。当从细胞中分离出来并加载铁时,这些晶体产生的磁场力比以前研究中使用的单个铁蛋白笼大 9 个数量级。这些蛋白晶体被施加的磁场吸引,并在被内化到细胞内时向磁铁移动。虽然还需要进一步的研究来实现磁遗传学的全部潜力,但这些结果证明了为磁传感工程设计蛋白组装体的可行性。