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大鼠交感神经元中与G蛋白亚基融合的绿色荧光蛋白的功能表达及荧光共振能量转移分析

Functional expression and FRET analysis of green fluorescent proteins fused to G-protein subunits in rat sympathetic neurons.

作者信息

Ruiz-Velasco V, Ikeda S R

机构信息

Laboratory of Molecular Physiology, Guthrie Research Institute, 1 Guthrie Square, Sayre, PA 18840, USA.

出版信息

J Physiol. 2001 Dec 15;537(Pt 3):679-92. doi: 10.1111/j.1469-7793.2001.00679.x.

Abstract
  1. cDNA constructs coding for a yellow-emitting green fluorescent protein (GFP) mutant fused to the N-terminus of the G-protein subunit beta 1 (YFP-beta 1) and a cyan-emitting GFP mutant fused to the N-terminus of the G-protein subunit gamma 2 (CFP-gamma 2) were heterologously expressed in rat superior cervical ganglion (SCG) neurons following intranuclear injection of the tagged subunits. The ability of the tagged subunits to modulate effectors, form a heterotrimer and couple to receptors was characterized using the whole-cell patch-clamp technique. Fluorescent resonance energy transfer (FRET) was also measured to determine the protein-protein interaction between the two fusion proteins. 2. Similar to co-expression of untagged beta 1/gamma 2, co-expression of YFP-beta 1/gamma 2, beta 1/CFP-gamma 2, or YFP-beta 1/CFP-gamma 2 resulted in a significant increase in basal N-type Ca(2+) channel facilitation when compared to uninjected neurons. Furthermore, the noradrenaline (NA)-mediated inhibition of Ca(2+) channels was significantly attenuated. 3. Co-expression of YFP-beta 1/CFP-gamma 2 with G-protein-gated inwardly rectifying K(+) channels (GIRK1 and GIRK4) resulted in tonic GIRK currents that were blocked by Ba(2+). 4. The ability of the tagged subunits to form heterotrimers was tested by co-injecting either tagged or untagged G beta 1 and G gamma 2 with excess G alpha(oA) cDNA. Under these conditions, the NA-mediated Ca(2+) current inhibition was significantly decreased when compared to uninjected neurons. 5. Coupling to the alpha 2-adrenergic receptor was reconstituted in neurons expressing pertussis toxin (PTX)-insensitive G alpha(oA) and either tagged or untagged G beta 1 gamma 2 subunits. Application of NA to PTX-treated cells resulted in a voltage-dependent inhibition of N-type Ca(2+) currents. 6. FRET measurements in the SCG revealed an in vivo interaction between YFP-beta 1 and CFP-gamma 2. Co-expression of untagged beta 1 significantly decreased the interaction between the two fusion proteins. 7. In summary, the attachment of GFP mutants to the N-terminus of G beta 1 or G gamma 2 does not qualitatively impair their ability to form a heterotrimer, modulate effectors (N-type Ca(2+) and GIRK channels), or couple to receptors.
摘要
  1. 将编码与G蛋白亚基β1的N端融合的黄色荧光蛋白(GFP)突变体的cDNA构建体和与G蛋白亚基γ2的N端融合的青色荧光蛋白(CFP)突变体在核内注射标记亚基后在大鼠颈上神经节(SCG)神经元中进行异源表达。使用全细胞膜片钳技术表征标记亚基调节效应器、形成异源三聚体以及与受体偶联的能力。还测量了荧光共振能量转移(FRET)以确定两种融合蛋白之间的蛋白质-蛋白质相互作用。2. 与未标记的β1/γ2共表达类似,YFP-β1/γ2、β1/CFP-γ2或YFP-β1/CFP-γ2共表达与未注射的神经元相比,导致基础N型Ca(2+)通道易化作用显著增加。此外,去甲肾上腺素(NA)介导的Ca(2+)通道抑制作用显著减弱。3. YFP-β1/CFP-γ2与G蛋白门控内向整流钾通道(GIRK1和GIRK4)共表达导致被Ba(2+)阻断的强直GIRK电流。4. 通过将标记的或未标记的Gβ1和Gγ2与过量的Gα(oA) cDNA共注射来测试标记亚基形成异源三聚体的能力。在这些条件下,与未注射的神经元相比,NA介导的Ca(2+)电流抑制作用显著降低。5. 在表达百日咳毒素(PTX)不敏感的Gα(oA)以及标记的或未标记的Gβ1γ2亚基的神经元中重建与α2-肾上腺素能受体的偶联。将NA应用于PTX处理的细胞导致N型Ca(2+)电流的电压依赖性抑制。6. SCG中的FRET测量揭示了YFP-β1和CFP-γ2之间的体内相互作用。未标记的β1共表达显著降低了两种融合蛋白之间的相互作用。7. 总之,将GFP突变体连接到Gβ1或Gγ2的N端在质量上不会损害它们形成异源三聚体、调节效应器(N型Ca(2+)和GIRK通道)或与受体偶联

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