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Fusion of synaptic vesicles and plasma membrane in the presence of synaptosomal soluble proteins
Fusion between synaptic vesicles and plasma membranes isolated from rat brain synaptosomes is regarded as a model of neurosecretion. The main aim of current study is to investigate whether the synaptosomal soluble proteins are essential members of Ca 2+-triggered fusion examined in this system. Fusi...
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Published in: | Neurochemistry international 2006-08, Vol.49 (3), p.270-275 |
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description | Fusion between synaptic vesicles and plasma membranes isolated from rat brain synaptosomes is regarded as a model of neurosecretion. The main aim of current study is to investigate whether the synaptosomal soluble proteins are essential members of Ca
2+-triggered fusion examined in this system.
Fusion experiments were performed using fluorescent dye octadecylrhodamine B, which was incorporated into synaptic vesicle membranes at self-quenching concentration. The fusion of synaptic vesicles, containing marker octadecylrhodamine B, with plasma membranes was detected by dequenching of the probe fluorescence. Membrane fusion was not found in Ca
2+-supplemented buffer solution, but was initiated by the addition of the synaptosomal soluble proteins. When soluble proteins were treated with trypsin, they lost completely the fusion activity. These experiments confirmed that soluble proteins of synaptosomes are sensitive to Ca
2+ signal and essential for membrane fusion. The experiments, in which members of fusion process were treated with monoclonal antibodies raised against synaptotagmin and synaptobrevin, have shown that antibodies only partially inhibited fusion of synaptic vesicles and plasma membranes in vitro. These results indicate that other additional component(s), which may or may not be related to synaptobrevin or synaptotagmin, mediate this process. It can be assumed that fusion of synaptic vesicles with plasma membranes in vitro depends upon the complex interaction of a large number of protein factors. |
doi_str_mv | 10.1016/j.neuint.2006.01.014 |
format | article |
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2+-triggered fusion examined in this system.
Fusion experiments were performed using fluorescent dye octadecylrhodamine B, which was incorporated into synaptic vesicle membranes at self-quenching concentration. The fusion of synaptic vesicles, containing marker octadecylrhodamine B, with plasma membranes was detected by dequenching of the probe fluorescence. Membrane fusion was not found in Ca
2+-supplemented buffer solution, but was initiated by the addition of the synaptosomal soluble proteins. When soluble proteins were treated with trypsin, they lost completely the fusion activity. These experiments confirmed that soluble proteins of synaptosomes are sensitive to Ca
2+ signal and essential for membrane fusion. The experiments, in which members of fusion process were treated with monoclonal antibodies raised against synaptotagmin and synaptobrevin, have shown that antibodies only partially inhibited fusion of synaptic vesicles and plasma membranes in vitro. These results indicate that other additional component(s), which may or may not be related to synaptobrevin or synaptotagmin, mediate this process. It can be assumed that fusion of synaptic vesicles with plasma membranes in vitro depends upon the complex interaction of a large number of protein factors.</description><identifier>ISSN: 0197-0186</identifier><identifier>EISSN: 1872-9754</identifier><identifier>DOI: 10.1016/j.neuint.2006.01.014</identifier><identifier>PMID: 16581156</identifier><identifier>CODEN: NEUIDS</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Animals ; Biological and medical sciences ; Cell Membrane - metabolism ; Cell-free model system ; Exocytosis ; Fundamental and applied biological sciences. Psychology ; Membrane fusion ; Membrane Fusion - physiology ; Membrane Proteins - metabolism ; Rats ; Rats, Wistar ; SNARE proteins ; SNARE Proteins - metabolism ; Solubility ; Synaptic Membranes - metabolism ; Synaptic Vesicles - metabolism ; Synaptosomes - metabolism ; Vertebrates: nervous system and sense organs</subject><ispartof>Neurochemistry international, 2006-08, Vol.49 (3), p.270-275</ispartof><rights>2006 Elsevier Ltd</rights><rights>2006 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c421t-27418d382e84861d11ff963caede76a80c565a81b68f12a761db0d1be08c61853</citedby><cites>FETCH-LOGICAL-c421t-27418d382e84861d11ff963caede76a80c565a81b68f12a761db0d1be08c61853</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17944612$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16581156$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Trikash, I.O.</creatorcontrib><creatorcontrib>Kolchinskaya, L.I.</creatorcontrib><title>Fusion of synaptic vesicles and plasma membrane in the presence of synaptosomal soluble proteins</title><title>Neurochemistry international</title><addtitle>Neurochem Int</addtitle><description>Fusion between synaptic vesicles and plasma membranes isolated from rat brain synaptosomes is regarded as a model of neurosecretion. The main aim of current study is to investigate whether the synaptosomal soluble proteins are essential members of Ca
2+-triggered fusion examined in this system.
Fusion experiments were performed using fluorescent dye octadecylrhodamine B, which was incorporated into synaptic vesicle membranes at self-quenching concentration. The fusion of synaptic vesicles, containing marker octadecylrhodamine B, with plasma membranes was detected by dequenching of the probe fluorescence. Membrane fusion was not found in Ca
2+-supplemented buffer solution, but was initiated by the addition of the synaptosomal soluble proteins. When soluble proteins were treated with trypsin, they lost completely the fusion activity. These experiments confirmed that soluble proteins of synaptosomes are sensitive to Ca
2+ signal and essential for membrane fusion. The experiments, in which members of fusion process were treated with monoclonal antibodies raised against synaptotagmin and synaptobrevin, have shown that antibodies only partially inhibited fusion of synaptic vesicles and plasma membranes in vitro. These results indicate that other additional component(s), which may or may not be related to synaptobrevin or synaptotagmin, mediate this process. It can be assumed that fusion of synaptic vesicles with plasma membranes in vitro depends upon the complex interaction of a large number of protein factors.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cell Membrane - metabolism</subject><subject>Cell-free model system</subject><subject>Exocytosis</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Membrane fusion</subject><subject>Membrane Fusion - physiology</subject><subject>Membrane Proteins - metabolism</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>SNARE proteins</subject><subject>SNARE Proteins - metabolism</subject><subject>Solubility</subject><subject>Synaptic Membranes - metabolism</subject><subject>Synaptic Vesicles - metabolism</subject><subject>Synaptosomes - metabolism</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0197-0186</issn><issn>1872-9754</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNqFkUGLFDEQhYMo7uzqPxDJRW89pjLpJH0RZHFdYcGLnmM6XY0Z0snY1b2w_34zzMDcFArq8r1XxXuMvQOxBQH6036bcY152Uoh9FZAHfWCbcAa2XSmVS_ZRkBnGgFWX7Fror0QwnSifc2uQLcWoNUb9vtupVgyLyOnp-wPSwz8ESmGhMR9HvgheZo8n3DqZ5-Rx8yXP8gPMxLmgBdhoTL5xKmktU9HoCwYM71hr0afCN-e9w37dff15-198_Dj2_fbLw9NUBKWRhoFdthZiVZZDQPAOHZ6FzwOaLS3IrS69RZ6bUeQ3lSkFwP0KGzQYNvdDft48q2H_65Ii5siBUypPl1WctpqaSzY_4JgpFJG7SqoTmCYC9GMozvMcfLzkwPhjhW4vTtV4I4VOAF1VJW9P_uv_YTDRXTOvAIfzoCn4NNYYw2RLpzplNIgK_f5xGGN7THi7CjEY-ZDnDEsbijx3588A-3Ap0k</recordid><startdate>20060801</startdate><enddate>20060801</enddate><creator>Trikash, I.O.</creator><creator>Kolchinskaya, L.I.</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7TK</scope><scope>7X8</scope></search><sort><creationdate>20060801</creationdate><title>Fusion of synaptic vesicles and plasma membrane in the presence of synaptosomal soluble proteins</title><author>Trikash, I.O. ; Kolchinskaya, L.I.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c421t-27418d382e84861d11ff963caede76a80c565a81b68f12a761db0d1be08c61853</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cell Membrane - metabolism</topic><topic>Cell-free model system</topic><topic>Exocytosis</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Membrane fusion</topic><topic>Membrane Fusion - physiology</topic><topic>Membrane Proteins - metabolism</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>SNARE proteins</topic><topic>SNARE Proteins - metabolism</topic><topic>Solubility</topic><topic>Synaptic Membranes - metabolism</topic><topic>Synaptic Vesicles - metabolism</topic><topic>Synaptosomes - metabolism</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Trikash, I.O.</creatorcontrib><creatorcontrib>Kolchinskaya, L.I.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Neurochemistry international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Trikash, I.O.</au><au>Kolchinskaya, L.I.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fusion of synaptic vesicles and plasma membrane in the presence of synaptosomal soluble proteins</atitle><jtitle>Neurochemistry international</jtitle><addtitle>Neurochem Int</addtitle><date>2006-08-01</date><risdate>2006</risdate><volume>49</volume><issue>3</issue><spage>270</spage><epage>275</epage><pages>270-275</pages><issn>0197-0186</issn><eissn>1872-9754</eissn><coden>NEUIDS</coden><abstract>Fusion between synaptic vesicles and plasma membranes isolated from rat brain synaptosomes is regarded as a model of neurosecretion. The main aim of current study is to investigate whether the synaptosomal soluble proteins are essential members of Ca
2+-triggered fusion examined in this system.
Fusion experiments were performed using fluorescent dye octadecylrhodamine B, which was incorporated into synaptic vesicle membranes at self-quenching concentration. The fusion of synaptic vesicles, containing marker octadecylrhodamine B, with plasma membranes was detected by dequenching of the probe fluorescence. Membrane fusion was not found in Ca
2+-supplemented buffer solution, but was initiated by the addition of the synaptosomal soluble proteins. When soluble proteins were treated with trypsin, they lost completely the fusion activity. These experiments confirmed that soluble proteins of synaptosomes are sensitive to Ca
2+ signal and essential for membrane fusion. The experiments, in which members of fusion process were treated with monoclonal antibodies raised against synaptotagmin and synaptobrevin, have shown that antibodies only partially inhibited fusion of synaptic vesicles and plasma membranes in vitro. These results indicate that other additional component(s), which may or may not be related to synaptobrevin or synaptotagmin, mediate this process. It can be assumed that fusion of synaptic vesicles with plasma membranes in vitro depends upon the complex interaction of a large number of protein factors.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>16581156</pmid><doi>10.1016/j.neuint.2006.01.014</doi><tpages>6</tpages></addata></record> |
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subjects | Animals Biological and medical sciences Cell Membrane - metabolism Cell-free model system Exocytosis Fundamental and applied biological sciences. Psychology Membrane fusion Membrane Fusion - physiology Membrane Proteins - metabolism Rats Rats, Wistar SNARE proteins SNARE Proteins - metabolism Solubility Synaptic Membranes - metabolism Synaptic Vesicles - metabolism Synaptosomes - metabolism Vertebrates: nervous system and sense organs |
title | Fusion of synaptic vesicles and plasma membrane in the presence of synaptosomal soluble proteins |
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