A genetically encoded sensor for H2O2 with expanded dynamic range

被引:135
作者
Markvicheva, Kseniya N. [1 ]
Bilan, Dmitry S. [1 ]
Mishina, Natalia M. [1 ]
Gorokhovatsky, Andrey Yu. [2 ]
Vinokurov, Leonid M. [2 ]
Lukyanov, Sergey [1 ]
Belousov, Vsevolod V. [1 ]
机构
[1] RAS, Shemyakin Ovchinnikov Inst Bioorgan Chem, Moscow 117997, Russia
[2] RAS, Pushchino Branch, Shemyakin Ovchinnikov Inst Bioorgan Chem, Pushchino, Russia
基金
俄罗斯基础研究基金会;
关键词
Hydrogen peroxide; HyPer; HyPer-2; OxyR; Imaging; GFP; TRANSCRIPTIONAL REGULATOR OXYR; DISULFIDE BOND FORMATION; MUTATIONAL ANALYSIS; REGIONS IMPORTANT; INACTIVATION; ACTIVATION; OXIDATION;
D O I
10.1016/j.bmc.2010.07.014
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hydrogen peroxide is an important second messenger controlling intracellular signaling cascades by selective oxidation of redox active thiolates in proteins. Changes in intracellular [H2O2] can be tracked in real time using HyPer, a ratiometric genetically encoded fluorescent probe. Although HyPer is sensitive and selective for H2O2 due to the properties of its sensing domain derived from the Escherichia coli OxyR protein, many applications may benefit from an improvement of the indicator's dynamic range. We here report HyPer-2, a probe that fills this demand. Upon saturating [H2O2] exposure, HyPer-2 undergoes an up to sixfold increase of the ratio F500/F420 versus a threefold change in HyPer. HyPer-2 was generated by a single point mutation A406V from HyPer corresponding to A233V in wtOxyR. This mutation was previously shown to destabilize interface between monomers in OxyR dimers. However, in HyPer-2, the A233V mutation stabilizes the dimer and expands the dynamic range of the probe. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1079 / 1084
页数:6
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