Using ApoE Nanolipoprotein Particles To Analyze SNARE-Induced Fusion Pores

Using ApoE Nanolipoprotein Particles To Analyze SNARE-Induced Fusion Pores

Here we introduce ApoE-based nanolipoprotein particle (NLP)-a soluble, discoidal bilayer mimetic of ∼23 nm in diameter, as fusion partners to study the dynamics of fusion pores induced by SNARE proteins. Using in vitro lipid mixing and content release assays, we report that NLPs reconstituted with s...

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Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1999. - 32(2016), 12 vom: 29. März, Seite 3015-23
1. Verfasser: Bello, Oscar D (VerfasserIn)
Weitere Verfasser: Auclair, Sarah M, Rothman, James E, Krishnakumar, Shyam S
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2016
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article Research Support, N.I.H., Extramural Apolipoproteins E Dextrans Fluorescent Dyes Liposomes Phosphatidylcholines Phosphatidylethanolamines Phosphatidylinositol 4,5-Diphosphate Phosphatidylinositols mehr... Phosphatidylserines Synaptosomal-Associated Protein 25 Syntaxin 1 Vesicle-Associated Membrane Protein 2 Dithionite 14844-07-6 N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl)phosphatidylethanolamine 64205-19-2 1,2-dioleoylphosphatidylserine 70614-14-1 Cholesterol 97C5T2UQ7J Calcium SY7Q814VUP 1-palmitoyl-2-oleoylphosphatidylcholine TE895536Y5 Dimyristoylphosphatidylcholine U86ZGC74V5 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphoethanolamine VM33LRU3A6
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100 1 |a Bello, Oscar D  |e verfasserin  |4 aut 
245 1 0 |a Using ApoE Nanolipoprotein Particles To Analyze SNARE-Induced Fusion Pores 
264 1 |c 2016 
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500 |a Date Revised 21.12.2018 
500 |a published: Print-Electronic 
500 |a Citation Status MEDLINE 
520 |a Here we introduce ApoE-based nanolipoprotein particle (NLP)-a soluble, discoidal bilayer mimetic of ∼23 nm in diameter, as fusion partners to study the dynamics of fusion pores induced by SNARE proteins. Using in vitro lipid mixing and content release assays, we report that NLPs reconstituted with synaptic v-SNARE VAMP2 (vNLP) fuse with liposomes containing the cognate t-SNARE (Syntaxin1/SNAP25) partner, with the resulting fusion pore opening directly to the external buffer. Efflux of encapsulated fluorescent dextrans of different sizes show that unlike the smaller nanodiscs, these larger NLPs accommodate the expansion of the fusion pore to at least ∼9 nm, and dithionite quenching of fluorescent lipid introduced in vNLP confirms that the NLP fusion pores are short-lived and eventually reseal. The NLPs also have capacity to accommodate larger number of proteins and using vNLPs with defined number of VAMP2 protein, including physiologically relevant copy numbers, we find that 3-4 copies of VAMP2 (minimum 2 per face) are required to keep a nascent fusion pore open, and the SNARE proteins act cooperatively to dilate the nascent fusion pore 
650 4 |a Journal Article 
650 4 |a Research Support, N.I.H., Extramural 
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650 7 |a Phosphatidylcholines  |2 NLM 
650 7 |a Phosphatidylethanolamines  |2 NLM 
650 7 |a Phosphatidylinositol 4,5-Diphosphate  |2 NLM 
650 7 |a Phosphatidylinositols  |2 NLM 
650 7 |a Phosphatidylserines  |2 NLM 
650 7 |a Synaptosomal-Associated Protein 25  |2 NLM 
650 7 |a Syntaxin 1  |2 NLM 
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650 7 |a 64205-19-2  |2 NLM 
650 7 |a 1,2-dioleoylphosphatidylserine  |2 NLM 
650 7 |a 70614-14-1  |2 NLM 
650 7 |a Cholesterol  |2 NLM 
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650 7 |a SY7Q814VUP  |2 NLM 
650 7 |a 1-palmitoyl-2-oleoylphosphatidylcholine  |2 NLM 
650 7 |a TE895536Y5  |2 NLM 
650 7 |a Dimyristoylphosphatidylcholine  |2 NLM 
650 7 |a U86ZGC74V5  |2 NLM 
650 7 |a 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphoethanolamine  |2 NLM 
650 7 |a VM33LRU3A6  |2 NLM 
700 1 |a Auclair, Sarah M  |e verfasserin  |4 aut 
700 1 |a Rothman, James E  |e verfasserin  |4 aut 
700 1 |a Krishnakumar, Shyam S  |e verfasserin  |4 aut 
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