Protein inhibitor of retinal membrane guanylyl cyclase suppresses cGMP synthesis in photoreceptors.

IF 4 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Igor V Peshenko,Elena V Olshevskaya,Alexander M Dizhoor
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引用次数: 0

Abstract

Retinal membrane guanylyl cyclase (RetGC) regulated by RetGC activating proteins (GCAPs) imparts light-sensitivity to rods and cones by producing cGMP to open cGMP-gated channels in the photoreceptor outer segments. However, excessive cGMP synthesis by deregulated RetGC:GCAP complex provokes cone-rod degeneration and causes congenital blindness. We developed the first to date specific protein inhibitor of retinal guanylyl cyclase (PIGCY) capable of reducing RetGC activity in photoreceptor outer segment. PIGCY was constructed by modifying GCAP1 to eliminate its ability to activate RetGC while increasing its affinity for RetGC. PIGCY uncouples RetGC1:GCAP1 complex in vitro, reducing Vmax and increasing KmGTP of RetGC activity. PIGCY inhibits both basal and GCAP-stimulated RetGC activity from wild type, GCAP1-/-, GCAP2-/-, and GCAPs-/- mouse retinas homogenates and in isolated rod outer segments (ROS). When expressed in mouse rods, PIGCY accumulates in outer segments and decelerates endogenous GCAP-stimulated RetGC activity in PIGCYTg retina.
视网膜膜鸟苷环化酶蛋白抑制剂抑制光感受器中cGMP的合成。
视网膜膜观酰基环化酶(RetGC)受RetGC激活蛋白(GCAPs)调控,通过产生cGMP打开感光器外节的cGMP门控通道,赋予视杆细胞和视锥细胞光敏性。然而,通过解除调控的RetGC:GCAP复合体合成过量的cGMP可引起锥杆变性并导致先天性失明。我们开发了迄今为止第一个能够降低光感受器外段RetGC活性的特异性视网膜观酰基环化酶(PIGCY)蛋白抑制剂。PIGCY是通过修饰GCAP1来消除其激活RetGC的能力,同时增加其对RetGC的亲和力来构建的。PIGCY在体外解耦RetGC1:GCAP1复合物,降低Vmax,增加RetGC活性的KmGTP。PIGCY抑制野生型、GCAP1-/-、GCAP2-/-和gcap -/-小鼠视网膜匀浆和离体杆外段(ROS)的基础和gcap刺激的RetGC活性。当在小鼠棒中表达时,PIGCY在外节段积累,并减缓内源性gcap刺激的PIGCYTg视网膜中的RetGC活性。
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来源期刊
Journal of Biological Chemistry
Journal of Biological Chemistry Biochemistry, Genetics and Molecular Biology-Biochemistry
自引率
4.20%
发文量
1233
期刊介绍: The Journal of Biological Chemistry welcomes high-quality science that seeks to elucidate the molecular and cellular basis of biological processes. Papers published in JBC can therefore fall under the umbrellas of not only biological chemistry, chemical biology, or biochemistry, but also allied disciplines such as biophysics, systems biology, RNA biology, immunology, microbiology, neurobiology, epigenetics, computational biology, ’omics, and many more. The outcome of our focus on papers that contribute novel and important mechanistic insights, rather than on a particular topic area, is that JBC is truly a melting pot for scientists across disciplines. In addition, JBC welcomes papers that describe methods that will help scientists push their biochemical inquiries forward and resources that will be of use to the research community.
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