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Dynamic landscape of the intracellular termini of acid-sensing ion channel 1a.


ABSTRACT: Acid-sensing ion channels (ASICs) are trimeric proton-gated sodium channels. Recently it has been shown that these channels play a role in necroptosis following prolonged acidic exposure like occurs in stroke. The C-terminus of the channel is thought to mediate necroptotic cell death through interaction with receptor interacting serine threonine kinase 1 (RIPK1). This interaction is suggested to be inhibited at rest via an interaction between the C-terminus and the N-terminus which blocks the RIPK1 binding site. Here, we use a combination of two transition metal ion FRET (tmFRET) methods to investigate the conformational dynamics of the termini while the channel is closed and desensitized. We do not find evidence that the termini are close enough to be bound while the channel is at rest and find that the termini may modestly move closer together when desensitized. At rest, the N-terminus adopts a conformation parallel to the membrane about 10 Å away. The C-terminus, including the distal end, may also spend time close to the membrane at rest. After prolonged acidification, the proximal portion of the N-terminus moves marginally closer to the membrane whereas the distal portion of the C-terminus swings away from the membrane. Together these data suggest that a new hypothesis for RIPK1 binding during stroke is needed.

SUBMITTER: Cullinan MM 

PROVIDER: S-EPMC10350031 | biostudies-literature | 2023 Jul

REPOSITORIES: biostudies-literature

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Dynamic landscape of the intracellular termini of acid-sensing ion channel 1a.

Cullinan Megan M MM   Klipp Robert C RC   Camenisch Abigail A   Bankston John R JR  

bioRxiv : the preprint server for biology 20230919


Acid-sensing ion channels (ASICs) are trimeric proton-gated sodium channels. Recently it has been shown that these channels play a role in necroptosis following prolonged acidic exposure like occurs in stroke. The C-terminus of the channel is thought to mediate necroptotic cell death through interaction with receptor interacting serine threonine kinase 1 (RIPK1). This interaction is hypothesized to be inhibited at rest via an interaction between the C-terminus and the N-terminus which blocks the  ...[more]

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