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Hi1a 调节酸敏感离子通道的机制。

Mechanism of acid-sensing ion channel modulation by Hi1a.

机构信息

Department of Biology, University of Rochester, Rochester, NY, USA.

Department of Pharmacology and Physiology, University of Rochester Medical Center, Rochester, NY, USA.

出版信息

J Gen Physiol. 2024 Dec 2;156(12). doi: 10.1085/jgp.202313519. Epub 2024 Oct 24.

Abstract

Acid-sensing ion channels (ASICs) are trimeric cation-selective channels activated by extracellular acidification. Amongst many pathological roles, ASICs are an important mediator of ischemic cell death and hence an attractive drug target for stroke treatment as well as other conditions. A peptide called Hi1a, isolated from Australian funnel web spider venom, inhibits ASIC1a and attenuates cell death in a stroke model up to 8 h after stroke induction. Here, we set out to understand the molecular basis for Hi1a's action. Hi1a is a bivalent toxin with two inhibitory cystine knot domains joined by a short linker. We found that both Hi1a domains modulate human ASIC1a gating with the N-terminal domain impairing channel activation while the C-terminal domain produces a "pro-open" phenotype even at submicromolar concentrations. Interestingly, both domains bind at the same site since a single point mutation, F352A, abolishes functional effects and reduces toxin affinity in surface plasmon resonance measurements. Therefore, the action of Hi1a at ASIC1a appears to arise through a mutually exclusive binding model where either the N or C domain of a single Hi1a binds one ASIC1a subunit. An ASIC1a trimer may bind several inhibitory N domains and one or more pro-open C domains at any one time, accounting for the incomplete inhibition of wild type Hi1a. We also found that the functional differences between these two domains are partially transferred by mutagenesis, affording new insight into the channel function and possible novel avenues of drug design.

摘要

酸敏离子通道(ASICs)是三聚体阳离子选择性通道,可被细胞外酸化激活。在许多病理作用中,ASICs 是缺血性细胞死亡的重要介导物,因此是治疗中风以及其他疾病的有吸引力的药物靶点。一种名为 Hi1a 的肽,从澳大利亚漏斗网蜘蛛毒液中分离出来,可抑制 ASIC1a,并在中风诱导后 8 小时内减轻中风模型中的细胞死亡。在这里,我们着手了解 Hi1a 作用的分子基础。Hi1a 是一种双价毒素,由两个抑制性半胱氨酸结结构域通过短连接子连接而成。我们发现,Hi1a 的两个结构域都可调节人类 ASIC1a 的门控作用,其中 N 端结构域损害通道激活,而 C 端结构域即使在亚微摩尔浓度下也会产生“预开放”表型。有趣的是,两个结构域都结合在同一部位,因为单个点突变 F352A 会消除功能效应并降低表面等离子体共振测量中的毒素亲和力。因此,Hi1a 在 ASIC1a 上的作用似乎是通过一种相互排斥的结合模式产生的,其中单个 Hi1a 的 N 或 C 结构域与一个 ASIC1a 亚基结合。一个 ASIC1a 三聚体可能同时结合几个抑制性 N 结构域和一个或多个预开放 C 结构域,这解释了野生型 Hi1a 不完全抑制的原因。我们还发现,这两个结构域之间的功能差异部分通过突变发生转移,为通道功能提供了新的见解,并为可能的新药设计开辟了新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4046/11513431/ea7118d38635/JGP_202313519_Fig1.jpg

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