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Article: Repurposing a pore: Highly conserved perforin-like proteins with alternative mechanisms

TitleRepurposing a pore: Highly conserved perforin-like proteins with alternative mechanisms
Authors
KeywordsAstrotactin
BRINP
Evolution
Perforin-like protein
Issue Date2017
Citation
Philosophical Transactions of the Royal Society B: Biological Sciences, 2017, v. 372, n. 1726, article no. 20160212 How to Cite?
AbstractPore-forming proteins play critical roles in pathogenic attack and immunological defence. The membrane attack complex/perforin (MACPF) group of homologues represents, with cholesterol-dependent cytolysins, the largest family of such proteins. In this review, we begin by describing briefly the structure of MACPF proteins, outlining their common mechanism of pore formation. We subsequently discuss some examples of MACPF proteins likely implicated in pore formation or other membrane-remodelling processes. Finally, we focus on astrotactin and bone morphogenetic protein and retinoic acid-induced neural-specific proteins, highly conserved MACPF family members involved in developmental processes, which have not been well studied to date or observed to form a pore-and which data suggest may act by alternative mechanisms. This article is part of the themed issue ‘Membrane pores: from structure and assembly, to medicine and technology’.
Persistent Identifierhttp://hdl.handle.net/10722/316472
ISSN
2023 Impact Factor: 5.4
2023 SCImago Journal Rankings: 2.035
PubMed Central ID
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorNi, Tao-
dc.contributor.authorGilbert, Robert J.C.-
dc.date.accessioned2022-09-14T11:40:31Z-
dc.date.available2022-09-14T11:40:31Z-
dc.date.issued2017-
dc.identifier.citationPhilosophical Transactions of the Royal Society B: Biological Sciences, 2017, v. 372, n. 1726, article no. 20160212-
dc.identifier.issn0962-8436-
dc.identifier.urihttp://hdl.handle.net/10722/316472-
dc.description.abstractPore-forming proteins play critical roles in pathogenic attack and immunological defence. The membrane attack complex/perforin (MACPF) group of homologues represents, with cholesterol-dependent cytolysins, the largest family of such proteins. In this review, we begin by describing briefly the structure of MACPF proteins, outlining their common mechanism of pore formation. We subsequently discuss some examples of MACPF proteins likely implicated in pore formation or other membrane-remodelling processes. Finally, we focus on astrotactin and bone morphogenetic protein and retinoic acid-induced neural-specific proteins, highly conserved MACPF family members involved in developmental processes, which have not been well studied to date or observed to form a pore-and which data suggest may act by alternative mechanisms. This article is part of the themed issue ‘Membrane pores: from structure and assembly, to medicine and technology’.-
dc.languageeng-
dc.relation.ispartofPhilosophical Transactions of the Royal Society B: Biological Sciences-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectAstrotactin-
dc.subjectBRINP-
dc.subjectEvolution-
dc.subjectPerforin-like protein-
dc.titleRepurposing a pore: Highly conserved perforin-like proteins with alternative mechanisms-
dc.typeArticle-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1098/rstb.2016.0212-
dc.identifier.pmid28630152-
dc.identifier.pmcidPMC5483515-
dc.identifier.scopuseid_2-s2.0-85021080181-
dc.identifier.volume372-
dc.identifier.issue1726-
dc.identifier.spagearticle no. 20160212-
dc.identifier.epagearticle no. 20160212-
dc.identifier.eissn1471-2970-
dc.identifier.isiWOS:000403552600005-

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