Abstract

Acid-sensing ion channels (ASICs) are cation-selective proton-gated channels expressed in neurons that participate in diverse physiological processes, including nociception, synaptic plasticity, learning, and memory. ASIC subunits contain intracellular N and C termini, two transmembrane domains that constitute the pore, and a large extracellular loop with defined domains termed the finger, β-ball, thumb, palm, and knuckle. Here we examined the contribution of the finger, β-ball, and thumb domains to activation and desensitization through the analysis of chimeras and the assessment of the effect of covalent modification of introduced Cys at the domain-domain interfaces. Our studies with ASIC1a-ASIC2a chimeras showed that swapping the thumb domain between subunits results in faster channel desensitization. Likewise, the covalent modification of Cys residues at selected positions in the β-ball-thumb interface accelerates the desensitization of the mutant channels. Studies of accessibility with thiol-reactive reagents revealed that the β-ball and thumb domains reside apart in the resting state but that they become closer to each other in response to extracellular acidification. We propose that the thumb domain moves upon continuous exposure to an acidic extracellular milieu, assisting with the closing of the pore during channel desensitization.

Highlights

  • (16), Huntington disease [17], Parkinson disease [18], and spinal cord injury [19]

  • Role of the Finger and Thumb Domains in Activation—Jasti et al [30] initially proposed that a cluster of adjacent acidic residues between the ␤-ball, thumb, and palm domains of chicken ASIC1 (cASIC1) served as proton-coordination sites

  • In addition to the mentioned region, we identified a proton coordination site in the lower palm domain of ASIC1a formed by residues Glu79 and Glu416 [46]

Read more

Summary

Mechanism of ASIC Desensitization

Given the importance of the thumb and neighboring domains to channel activation and desensitization, we examined their contribution to these processes through the analysis of ASIC1a-ASIC2a chimeras, by assessing the effect of covalent modification of introduced Cys at the finger-thumb and ␤-ballthumb interfaces, and through studies of accessibility with thiol-reactive reagents in the resting and desensitized states. Our data indicate that the introduction of structural changes at the ␤-ball-thumb interface accelerates channel desensitization. Studies with thiol-reactive reagents showed a change in accessibility in the thumb domain when the channel transitions from the resting to the desensitized state. Based on these results, we propose that the thumb domain moves in response to extracellular acidification to contain the movements of the ␤-ball and palm domains. Our data indicate that the thumb domain plays an essential role in the process that shuts down ion conduction during desensitization

Experimental Procedures
Results
Discussion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call