Type I Brain Hexokinase: Axonal Transport and Membrane Associations Within Central Nervous System Presynaptic Terminals
: While studying the delivery of cytoplasmic proteins to the presynaptic terminals of CNS neurons, we discovered unique characteristics of one protein (p118) conveyed in slow component b (SCb) of axonal transport, the large group of proteins representing the cytoplasmic matrix. Alone among the SCb g...
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Veröffentlicht in: | Journal of neurochemistry 1996-08, Vol.67 (2), p.845-856 |
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description | : While studying the delivery of cytoplasmic proteins to the presynaptic terminals of CNS neurons, we discovered unique characteristics of one protein (p118) conveyed in slow component b (SCb) of axonal transport, the large group of proteins representing the cytoplasmic matrix. Alone among the SCb group, p118 coisolated with the synaptic junctional complex on biochemical fractionation of the radiolabeled synaptic regions. Purification and amino acid sequencing of this protein revealed it is most likely the guinea pig form of type I (brain) hexokinase (ATP:d‐hexose 6‐phosphotransferase, EC 2.7.1.1). Further biochemical treatments were consistent with this identity. The majority of type I brain hexokinase has been thought to be associated primarily with membranes, in particular the mitochondrial outer membrane. We found that the majority of type I hexokinase is transported toward the terminals at a rate at least 10 times slower than that exhibited by the maximal or average rate of mitochondria. This suggests that, in the axon, the enzyme exhibits transient or dynamic interactions with mitochondria that are moving more rapidly. It is not clear whether hexokinase binds exclusively to mitochondria, or also exhibits association with nonmitochondrial membranes. The unexpected enrichment of hexokinase during synaptic junctional complex purification may result from its strong association with the presynaptic membrane portion of the synapse. |
doi_str_mv | 10.1046/j.1471-4159.1996.67020845.x |
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Alone among the SCb group, p118 coisolated with the synaptic junctional complex on biochemical fractionation of the radiolabeled synaptic regions. Purification and amino acid sequencing of this protein revealed it is most likely the guinea pig form of type I (brain) hexokinase (ATP:d‐hexose 6‐phosphotransferase, EC 2.7.1.1). Further biochemical treatments were consistent with this identity. The majority of type I brain hexokinase has been thought to be associated primarily with membranes, in particular the mitochondrial outer membrane. We found that the majority of type I hexokinase is transported toward the terminals at a rate at least 10 times slower than that exhibited by the maximal or average rate of mitochondria. This suggests that, in the axon, the enzyme exhibits transient or dynamic interactions with mitochondria that are moving more rapidly. It is not clear whether hexokinase binds exclusively to mitochondria, or also exhibits association with nonmitochondrial membranes. The unexpected enrichment of hexokinase during synaptic junctional complex purification may result from its strong association with the presynaptic membrane portion of the synapse.</description><identifier>ISSN: 0022-3042</identifier><identifier>EISSN: 1471-4159</identifier><identifier>DOI: 10.1046/j.1471-4159.1996.67020845.x</identifier><identifier>PMID: 8764615</identifier><identifier>CODEN: JONRA9</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Science Ltd</publisher><subject>Amino Acid Sequence ; Animals ; Axonal Transport ; Biochemistry and metabolism ; Biological and medical sciences ; Brain - enzymology ; Cattle ; Cell Compartmentation ; Central nervous system ; Fundamental and applied biological sciences. Psychology ; Guinea Pigs ; Hexokinase ; Hexokinase - metabolism ; Isoenzymes - metabolism ; Macromolecular Substances ; Male ; Mitochondria - enzymology ; Molecular Sequence Data ; Nerve Tissue Proteins - metabolism ; Presynaptic terminal ; Rats ; Sequence Alignment ; Sequence Homology, Amino Acid ; Synaptic junctional complex ; Vertebrates: nervous system and sense organs</subject><ispartof>Journal of neurochemistry, 1996-08, Vol.67 (2), p.845-856</ispartof><rights>1996 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4375-82e4d596915b6049197e39549b360105df26acb4f62a0a9782c7093636aeb4f63</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1046%2Fj.1471-4159.1996.67020845.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1046%2Fj.1471-4159.1996.67020845.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,781,785,1418,27928,27929,45578,45579</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3198447$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8764615$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Garner, Judy A.</creatorcontrib><creatorcontrib>Linse, Klaus D.</creatorcontrib><creatorcontrib>Polk, Roberta K.</creatorcontrib><title>Type I Brain Hexokinase: Axonal Transport and Membrane Associations Within Central Nervous System Presynaptic Terminals</title><title>Journal of neurochemistry</title><addtitle>J Neurochem</addtitle><description>: While studying the delivery of cytoplasmic proteins to the presynaptic terminals of CNS neurons, we discovered unique characteristics of one protein (p118) conveyed in slow component b (SCb) of axonal transport, the large group of proteins representing the cytoplasmic matrix. Alone among the SCb group, p118 coisolated with the synaptic junctional complex on biochemical fractionation of the radiolabeled synaptic regions. Purification and amino acid sequencing of this protein revealed it is most likely the guinea pig form of type I (brain) hexokinase (ATP:d‐hexose 6‐phosphotransferase, EC 2.7.1.1). Further biochemical treatments were consistent with this identity. The majority of type I brain hexokinase has been thought to be associated primarily with membranes, in particular the mitochondrial outer membrane. We found that the majority of type I hexokinase is transported toward the terminals at a rate at least 10 times slower than that exhibited by the maximal or average rate of mitochondria. This suggests that, in the axon, the enzyme exhibits transient or dynamic interactions with mitochondria that are moving more rapidly. It is not clear whether hexokinase binds exclusively to mitochondria, or also exhibits association with nonmitochondrial membranes. The unexpected enrichment of hexokinase during synaptic junctional complex purification may result from its strong association with the presynaptic membrane portion of the synapse.</description><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Axonal Transport</subject><subject>Biochemistry and metabolism</subject><subject>Biological and medical sciences</subject><subject>Brain - enzymology</subject><subject>Cattle</subject><subject>Cell Compartmentation</subject><subject>Central nervous system</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Guinea Pigs</subject><subject>Hexokinase</subject><subject>Hexokinase - metabolism</subject><subject>Isoenzymes - metabolism</subject><subject>Macromolecular Substances</subject><subject>Male</subject><subject>Mitochondria - enzymology</subject><subject>Molecular Sequence Data</subject><subject>Nerve Tissue Proteins - metabolism</subject><subject>Presynaptic terminal</subject><subject>Rats</subject><subject>Sequence Alignment</subject><subject>Sequence Homology, Amino Acid</subject><subject>Synaptic junctional complex</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0022-3042</issn><issn>1471-4159</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVUU1vEzEUtBCohMJPQLIE4raLvf5awymElhaVgkQQR8vrvBUO-4W9odl_j5ekuSJOz34z897Yg9ALSnJKuHy9zSlXNONU6JxqLXOpSEFKLvL9A7Q4YQ_RgpCiyBjhxWP0JMYtIVRySc_QWanmg1igu_U0AL7G74L1Hb6Cff_TdzbCG7zc951t8DrYLg59GLHtNvgTtFVqAF7G2DtvR993EX_344-kXkE3hiS5hfC730X8dYojtPhLgDh1dhi9w2sIbZrfxKfoUZ0KPDvWc_Tt8mK9uspuPn-4Xi1vMseZEllZAN8ILTUVlSRcU62AacF1xSShRGzqQlpX8VoWllitysIpoplk0sLcZefo1WHuEPpfO4ijaX100DTpEcmjSQqmSqb-SaSilELwmfj2QHShjzFAbYbgWxsmQ4mZ8zFbM2dg5gzMnI-5z8fsk_r5cc2uamFz0h4DSfjLI26js02dPtv5eKIxqkv-18T7A-3ONzD9jwPz8XZ1f2N_APy9rSM</recordid><startdate>199608</startdate><enddate>199608</enddate><creator>Garner, Judy A.</creator><creator>Linse, Klaus D.</creator><creator>Polk, Roberta K.</creator><general>Blackwell Science Ltd</general><general>Blackwell</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>7TK</scope><scope>7X8</scope></search><sort><creationdate>199608</creationdate><title>Type I Brain Hexokinase: Axonal Transport and Membrane Associations Within Central Nervous System Presynaptic Terminals</title><author>Garner, Judy A. ; Linse, Klaus D. ; Polk, Roberta K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4375-82e4d596915b6049197e39549b360105df26acb4f62a0a9782c7093636aeb4f63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Axonal Transport</topic><topic>Biochemistry and metabolism</topic><topic>Biological and medical sciences</topic><topic>Brain - enzymology</topic><topic>Cattle</topic><topic>Cell Compartmentation</topic><topic>Central nervous system</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Guinea Pigs</topic><topic>Hexokinase</topic><topic>Hexokinase - metabolism</topic><topic>Isoenzymes - metabolism</topic><topic>Macromolecular Substances</topic><topic>Male</topic><topic>Mitochondria - enzymology</topic><topic>Molecular Sequence Data</topic><topic>Nerve Tissue Proteins - metabolism</topic><topic>Presynaptic terminal</topic><topic>Rats</topic><topic>Sequence Alignment</topic><topic>Sequence Homology, Amino Acid</topic><topic>Synaptic junctional complex</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Garner, Judy A.</creatorcontrib><creatorcontrib>Linse, Klaus D.</creatorcontrib><creatorcontrib>Polk, Roberta K.</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>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of neurochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Garner, Judy A.</au><au>Linse, Klaus D.</au><au>Polk, Roberta K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Type I Brain Hexokinase: Axonal Transport and Membrane Associations Within Central Nervous System Presynaptic Terminals</atitle><jtitle>Journal of neurochemistry</jtitle><addtitle>J Neurochem</addtitle><date>1996-08</date><risdate>1996</risdate><volume>67</volume><issue>2</issue><spage>845</spage><epage>856</epage><pages>845-856</pages><issn>0022-3042</issn><eissn>1471-4159</eissn><coden>JONRA9</coden><abstract>: While studying the delivery of cytoplasmic proteins to the presynaptic terminals of CNS neurons, we discovered unique characteristics of one protein (p118) conveyed in slow component b (SCb) of axonal transport, the large group of proteins representing the cytoplasmic matrix. Alone among the SCb group, p118 coisolated with the synaptic junctional complex on biochemical fractionation of the radiolabeled synaptic regions. Purification and amino acid sequencing of this protein revealed it is most likely the guinea pig form of type I (brain) hexokinase (ATP:d‐hexose 6‐phosphotransferase, EC 2.7.1.1). Further biochemical treatments were consistent with this identity. The majority of type I brain hexokinase has been thought to be associated primarily with membranes, in particular the mitochondrial outer membrane. We found that the majority of type I hexokinase is transported toward the terminals at a rate at least 10 times slower than that exhibited by the maximal or average rate of mitochondria. This suggests that, in the axon, the enzyme exhibits transient or dynamic interactions with mitochondria that are moving more rapidly. It is not clear whether hexokinase binds exclusively to mitochondria, or also exhibits association with nonmitochondrial membranes. The unexpected enrichment of hexokinase during synaptic junctional complex purification may result from its strong association with the presynaptic membrane portion of the synapse.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science Ltd</pub><pmid>8764615</pmid><doi>10.1046/j.1471-4159.1996.67020845.x</doi><tpages>12</tpages></addata></record> |
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subjects | Amino Acid Sequence Animals Axonal Transport Biochemistry and metabolism Biological and medical sciences Brain - enzymology Cattle Cell Compartmentation Central nervous system Fundamental and applied biological sciences. Psychology Guinea Pigs Hexokinase Hexokinase - metabolism Isoenzymes - metabolism Macromolecular Substances Male Mitochondria - enzymology Molecular Sequence Data Nerve Tissue Proteins - metabolism Presynaptic terminal Rats Sequence Alignment Sequence Homology, Amino Acid Synaptic junctional complex Vertebrates: nervous system and sense organs |
title | Type I Brain Hexokinase: Axonal Transport and Membrane Associations Within Central Nervous System Presynaptic Terminals |
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