Fluorescent indicators for inositol 1,4,5-trisphosphate based on bioconjugates of pleckstrin homology domain and fluorescent dyes

K. Hirose, H. Takeshima, M. Iino
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引用次数: 5

Abstract

Bioconjugates of fluorescent dyes and the recombinant pleckstrin homology (PH) domain of phospholipase Cδ1 were produced with the aim of developing a method to quantify inositol 1,4,5-trisphosphate (IP3) in biological samples. We replaced Cys-96 of the PH domain with Ser while retaining Cys-48 to which thiol-reactive fluorescent dyes can be coupled specifically. Acrylodan- and Dapoxyl-labelled C96S PH domain mutants exhibited fluorescence upon UV illumination with an emission peak at wavelengths of 505 and 514 nm, respectively. IP3 induced decreases in the fluorescence intensity with a red shift in the emission spectra. The dissociation constants (Kds) of the acrylodan- and Dapoxyl-labelled PH domains for IP3 were 659 and 586 nM, respectively. An additional mutation (C96S/V58K) in the PH domain decreased the Kds by ≡50%, providing a more sensitive method. The results indicate that these bioconjugates are promising as fluorescent indicators for IP3 quantification.
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基于pleckstrin同源结构域生物偶联物和荧光染料的1,4,5-三磷酸肌醇荧光指示剂
为了建立一种定量测定生物样品中肌醇1,4,5-三磷酸(IP3)的方法,制备了荧光染料的生物偶联物和重组磷脂酶Cδ1的pleckstrin同源(PH)结构域。我们用丝氨酸取代了PH结构域的Cys-96,同时保留了可与巯基反应性荧光染料特异性偶联的Cys-48。在紫外照射下,丙烯醛标记的C96S PH结构域突变体和达泊酚标记的C96S PH结构域突变体分别在505 nm和514 nm处显示荧光。IP3诱导荧光强度降低,发射光谱发生红移。IP3的丙烯醛和达泊酚标记的PH结构域的解离常数(Kds)分别为659 nM和586 nM。PH结构域的另一个突变(C96S/V58K)使Kds降低了≡50%,提供了一种更敏感的方法。结果表明,这些生物偶联物很有希望作为IP3定量的荧光指标。
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