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Positional editing of transmembrane domains during ion channel assembly
Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för biokemi och biofysik.
Vise andre og tillknytning
2013 (engelsk)Inngår i: Journal of Cell Science, ISSN 0021-9533, E-ISSN 1477-9137, Vol. 126, nr 2, s. 464-472Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

The integration of transmembrane (TM)-spanning regions of many channels and ion transporters is potentially compromised by the presence of polar and charged residues required for biological function. Although the two TMs of the ATP-gated ion channel subunit P2X2 each contain charged/polar amino acids, we found that each TM is efficiently membrane inserted when it is analysed in isolation, and uncovered no evidence for cooperativity between these two TMs during P2X2 integration. However, using minimal N-glycosylation distance mapping, we find that the positioning of TM2 in newly synthesized P2X2 monomers is distinct from that seen in subunits of the high-resolution structures of assembled homologous trimers. We conclude that P2X2 monomers are initially synthesised at the endoplasmic reticulum in a distinct conformation, where the extent of the TM-spanning regions is primarily defined by the thermodynamic cost of their membrane integration at the Sec61 translocon. In this model, TM2 of P2X2 subsequently undergoes a process of positional editing within the membrane that correlates with trimerisation of the monomer, a process requiring specific polar/charged residues in both TM1 and TM2. We postulate that the assembly process offsets any energetic cost of relocating TM2, and find evidence that positional editing of TM2 in the acid-sensing ion channel (ASIC1a) is even more pronounced than that observed for P2X2. Taken together, these data further underline the potential complexities involved in accurately predicting TM domains. We propose that the orchestrated repositioning of TM segments during subunit oligomerisation plays an important role in generating the functional architecture of active ion channels, and suggest that the regulation of this underappreciated biosynthetic step may provide an elegant mechanism for maintaining ER homeostasis.

sted, utgiver, år, opplag, sider
2013. Vol. 126, nr 2, s. 464-472
Emneord [en]
ASIC, Endoplasmic reticulum, Membrane insertion, Oligomerisation, P2X channels
HSV kategori
Identifikatorer
URN: urn:nbn:se:su:diva-89741DOI: 10.1242/jcs.111773ISI: 000316945600010OAI: oai:DiVA.org:su-89741DiVA, id: diva2:619985
Forskningsfinansiär
Swedish Cancer Society, 120837Swedish Research Council, 621-2010-5250Swedish Foundation for Strategic Research , A3-05:200EU, European Research Council, ERC-2008-AdG 232648
Merknad

AuthorCount:7;

Tilgjengelig fra: 2013-05-07 Laget: 2013-05-06 Sist oppdatert: 2022-03-23bibliografisk kontrollert

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Öjemalm, Karinvon Heijne, Gunnar

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