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本文引用的文献

1
Chromophore aspartate oxidation-decarboxylation in the green-to-red conversion of a fluorescent protein from Zoanthus sp. 2.来自绿纽扣珊瑚2号荧光蛋白从绿色到红色转变过程中的发色团天冬氨酸氧化脱羧作用。
Biochemistry. 2007 Oct 16;46(41):11528-35. doi: 10.1021/bi700721x. Epub 2007 Sep 25.
2
Refined crystal structures of red and green fluorescent proteins from the button polyp Zoanthus.来自纽扣海葵(Zoanthus)的红色和绿色荧光蛋白的精细晶体结构。
Acta Crystallogr D Biol Crystallogr. 2007 Oct;63(Pt 10):1082-93. doi: 10.1107/S0907444907042461. Epub 2007 Sep 19.
3
Crystallographic evidence for water-assisted photo-induced peptide cleavage in the stony coral fluorescent protein Kaede.石珊瑚荧光蛋白Kaede中光辅助水诱导肽裂解的晶体学证据。
J Mol Biol. 2007 Sep 28;372(4):918-926. doi: 10.1016/j.jmb.2007.06.037. Epub 2007 Jun 19.
4
Bright monomeric red fluorescent protein with an extended fluorescence lifetime.具有延长荧光寿命的明亮单体红色荧光蛋白。
Nat Methods. 2007 Jul;4(7):555-7. doi: 10.1038/nmeth1062. Epub 2007 Jun 17.
5
Chromophore structure of the kindling fluorescent protein asFP595 from Anemonia sulcata.来自沟迎风海葵的点燃荧光蛋白 asFP595 的发色团结构。
J Am Chem Soc. 2007 Jun 27;129(25):7748-9. doi: 10.1021/ja071992c. Epub 2007 May 31.
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Fluorescent proteins: maturation, photochemistry and photophysics.荧光蛋白:成熟、光化学与光物理
Curr Opin Struct Biol. 2006 Dec;16(6):714-21. doi: 10.1016/j.sbi.2006.10.001. Epub 2006 Oct 24.
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Novel chromophores and buried charges control color in mFruits.新型发色团和埋藏电荷控制着微型水果的颜色。
Biochemistry. 2006 Aug 15;45(32):9639-47. doi: 10.1021/bi060773l.
8
In vivo oxygen imaging using green fluorescent protein.利用绿色荧光蛋白进行体内氧成像。
Am J Physiol Cell Physiol. 2006 Oct;291(4):C781-7. doi: 10.1152/ajpcell.00067.2006. Epub 2006 May 31.
9
Structure of a red fluorescent protein from Zoanthus, zRFP574, reveals a novel chromophore.来自纽扣珊瑚的红色荧光蛋白zRFP574的结构揭示了一种新型发色团。
Acta Crystallogr D Biol Crystallogr. 2006 May;62(Pt 5):527-32. doi: 10.1107/S0907444906007852. Epub 2006 Apr 19.
10
Engineering of a monomeric green-to-red photoactivatable fluorescent protein induced by blue light.蓝光诱导的单体绿色到红色光激活荧光蛋白的工程改造。
Nat Biotechnol. 2006 Apr;24(4):461-5. doi: 10.1038/nbt1191. Epub 2006 Mar 19.

维多利亚多管水母绿色荧光蛋白的首个形成红色发色团的突变体。

The first mutant of the Aequorea victoria green fluorescent protein that forms a red chromophore.

作者信息

Mishin Alexander S, Subach Fedor V, Yampolsky Ilia V, King William, Lukyanov Konstantin A, Verkhusha Vladislav V

机构信息

Shemiakin-Ovchinnikov Institute of Bioorganic Chemistry, Miklukho-Maklaya 16/10, Moscow 117997, Russia.

出版信息

Biochemistry. 2008 Apr 22;47(16):4666-73. doi: 10.1021/bi702130s. Epub 2008 Mar 27.

DOI:10.1021/bi702130s
PMID:18366185
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2900791/
Abstract

Green fluorescent protein (GFP) from a jellyfish, Aequorea victoria, and its mutants are widely used in biomedical studies as fluorescent markers. In spite of the enormous efforts of academia and industry toward generating its red fluorescent mutants, no GFP variants with emission maximum at more than 529 nm have been developed during the 15 years since its cloning. Here, we used a new strategy of molecular evolution aimed at generating a red-emitting mutant of GFP. As a result, we have succeeded in producing the first GFP mutant that substantially matures to the red-emitting state with excitation and emission maxima at 555 and 585 nm, respectively. A novel, nonoxidative mechanism for formation of the red chromophore in this mutant that includes a dehydration of the Ser65 side chain has been proposed. Model experiments showed that the novel dual-color GFP mutant with green and red emission is suitable for multicolor flow cytometry as an additional color since it is clearly separable from both green and red fluorescent tags.

摘要

来自维多利亚多管水母的绿色荧光蛋白(GFP)及其突变体作为荧光标记物在生物医学研究中被广泛应用。尽管学术界和工业界为生成其红色荧光突变体付出了巨大努力,但自其克隆后的15年里,尚未开发出最大发射波长超过529nm的GFP变体。在此,我们采用了一种新的分子进化策略来生成GFP的红色发射突变体。结果,我们成功制备出了首个GFP突变体,它能基本成熟至红色发射状态,其激发和发射最大值分别为555nm和585nm。已提出一种在该突变体中形成红色发色团的新型非氧化机制,其中包括Ser65侧链的脱水。模型实验表明,这种具有绿色和红色发射的新型双色GFP突变体适合作为额外的一种颜色用于多色流式细胞术,因为它能与绿色和红色荧光标签清晰区分。