{"title":"Hi1a 对酸感应离子通道的调节机制","authors":"Kyle D Berger, David M MacLean","doi":"10.1085/jgp.202313519","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":54828,"journal":{"name":"Journal of General Physiology","volume":"156 12","pages":""},"PeriodicalIF":3.3000,"publicationDate":"2024-12-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11513431/pdf/","citationCount":"0","resultStr":"{\"title\":\"Mechanism of acid-sensing ion channel modulation by Hi1a.\",\"authors\":\"Kyle D Berger, David M MacLean\",\"doi\":\"10.1085/jgp.202313519\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>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. 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引用次数: 0
摘要
酸感应离子通道(ASIC)是由细胞外酸化激活的三聚阳离子选择性通道。在许多病理作用中,ASIC 是缺血性细胞死亡的重要介质,因此是治疗中风和其他疾病的一个有吸引力的药物靶点。从澳大利亚漏网蜘蛛毒液中分离出的一种名为 Hi1a 的多肽能抑制 ASIC1a,并在中风诱导后 8 小时内减轻中风模型中的细胞死亡。在此,我们着手了解 Hi1a 作用的分子基础。Hi1a 是一种二价毒素,有两个抑制性胱氨酸结结构域,由一个短连接体连接。我们发现,Hi1a 的两个结构域都能调节人类 ASIC1a 的门控,其中 N 端结构域会损害通道的激活,而 C 端结构域即使在亚摩尔浓度下也会产生 "促进开放 "的表型。有趣的是,这两个结构域结合在同一个位点,因为单点突变 F352A 在表面等离子体共振测量中取消了功能效应并降低了毒素亲和力。因此,Hi1a 对 ASIC1a 的作用似乎是通过一种相互排斥的结合模式产生的,即单个 Hi1a 的 N 或 C 结构域与一个 ASIC1a 亚基结合。ASIC1a 三聚体可能同时结合多个抑制性 N 结构域和一个或多个促进开放的 C 结构域,这就是野生型 Hi1a 抑制作用不完全的原因。我们还发现,这两个结构域之间的功能差异可通过诱变进行部分转移,从而为了解通道功能提供了新的视角,并为药物设计提供了可能的新途径。
Mechanism of acid-sensing ion channel modulation by Hi1a.
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.
期刊介绍:
General physiology is the study of biological mechanisms through analytical investigations, which decipher the molecular and cellular mechanisms underlying biological function at all levels of organization.
The mission of Journal of General Physiology (JGP) is to publish mechanistic and quantitative molecular and cellular physiology of the highest quality, to provide a best-in-class author experience, and to nurture future generations of independent researchers. The major emphasis is on physiological problems at the cellular and molecular level.