The design and delivery of a thermally responsive peptide to inhibit S100B-mediated neurodegeneration
Abstract S100B, a glial-secreted protein, is believed to play a major role in neurodegeneration in Alzheimer's disease, Down syndrome, traumatic brain injury, and spinocerebellar ataxia type 1 (SCA1). SCA1 is a trinucleotide repeat disorder in which the expanded polyglutamine mutation in the pr...
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description | Abstract S100B, a glial-secreted protein, is believed to play a major role in neurodegeneration in Alzheimer's disease, Down syndrome, traumatic brain injury, and spinocerebellar ataxia type 1 (SCA1). SCA1 is a trinucleotide repeat disorder in which the expanded polyglutamine mutation in the protein ataxin-1 primarily targets Purkinje cells of the cerebellum. Currently, the exact mechanism of S100B-mediated Purkinje cell damage in SCA1 is not clear. However, here we show that S100B may act via the activation of the receptor for advanced glycation end product (RAGE) signaling pathway, resulting in oxidative stress-mediated injury to mutant ataxin-1-expressing neurons. To combat S100B-mediated neurodegeneration, we have designed a selective thermally responsive S100B inhibitory peptide, Synb1-ELP-TRTK. Our therapeutic polypeptide was developed using three key elements: (1) the elastin-like polypeptide (ELP), a thermally responsive polypeptide, (2) the TRTK12 peptide, a known S100B inhibitory peptide, and (3) a cell-penetrating peptide, Synb1, to enhance intracellular delivery. Binding studies revealed that our peptide, Synb1-ELP-TRTK, interacts with its molecular target S100B and maintains a high S100B binding affinity as comparable with the TRTK12 peptide alone. In addition, in vitro studies revealed that Synb1-ELP-TRTK treatment reduces S100B uptake in SHSY5Y cells. Furthermore, the Synb1-ELP-TRTK peptide decreased S100B-induced oxidative damage to mutant ataxin-1-expressing neurons. To test the delivery capabilities of ELP-based therapeutic peptides to the cerebellum, we treated mice with fluorescently labeled Synb1-ELP and observed that thermal targeting enhanced peptide delivery to the cerebellum. Here, we have laid the framework for thermal-based therapeutic targeting to regions of the brain, particularly the cerebellum. Overall, our data suggest that thermal targeting of ELP-based therapeutic peptides to the cerebellum is a novel treatment strategy for cerebellar neurodegenerative disorders. |
doi_str_mv | 10.1016/j.neuroscience.2011.09.025 |
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SCA1 is a trinucleotide repeat disorder in which the expanded polyglutamine mutation in the protein ataxin-1 primarily targets Purkinje cells of the cerebellum. Currently, the exact mechanism of S100B-mediated Purkinje cell damage in SCA1 is not clear. However, here we show that S100B may act via the activation of the receptor for advanced glycation end product (RAGE) signaling pathway, resulting in oxidative stress-mediated injury to mutant ataxin-1-expressing neurons. To combat S100B-mediated neurodegeneration, we have designed a selective thermally responsive S100B inhibitory peptide, Synb1-ELP-TRTK. Our therapeutic polypeptide was developed using three key elements: (1) the elastin-like polypeptide (ELP), a thermally responsive polypeptide, (2) the TRTK12 peptide, a known S100B inhibitory peptide, and (3) a cell-penetrating peptide, Synb1, to enhance intracellular delivery. Binding studies revealed that our peptide, Synb1-ELP-TRTK, interacts with its molecular target S100B and maintains a high S100B binding affinity as comparable with the TRTK12 peptide alone. In addition, in vitro studies revealed that Synb1-ELP-TRTK treatment reduces S100B uptake in SHSY5Y cells. Furthermore, the Synb1-ELP-TRTK peptide decreased S100B-induced oxidative damage to mutant ataxin-1-expressing neurons. To test the delivery capabilities of ELP-based therapeutic peptides to the cerebellum, we treated mice with fluorescently labeled Synb1-ELP and observed that thermal targeting enhanced peptide delivery to the cerebellum. Here, we have laid the framework for thermal-based therapeutic targeting to regions of the brain, particularly the cerebellum. Overall, our data suggest that thermal targeting of ELP-based therapeutic peptides to the cerebellum is a novel treatment strategy for cerebellar neurodegenerative disorders.</description><identifier>ISSN: 0306-4522</identifier><identifier>EISSN: 1873-7544</identifier><identifier>DOI: 10.1016/j.neuroscience.2011.09.025</identifier><identifier>PMID: 21958864</identifier><identifier>CODEN: NRSCDN</identifier><language>eng</language><publisher>Amsterdam: Elsevier Ltd</publisher><subject>Animals ; Biological and medical sciences ; CapZ Actin Capping Protein ; Cell Line ; cerebellum ; Drug Design ; elastin-like polypeptide ; Fundamental and applied biological sciences. Psychology ; Humans ; Immunoblotting ; Mice ; Nerve Degeneration - prevention & control ; Nerve Growth Factors - antagonists & inhibitors ; neurodegeneration ; Neurology ; Neuroprotective Agents - chemical synthesis ; Neuroprotective Agents - metabolism ; Neuroprotective Agents - pharmacology ; Oligopeptides - metabolism ; Oligopeptides - pharmacology ; Peptide Fragments ; Protein Binding - physiology ; Proteins - metabolism ; Proteins - pharmacology ; S100 Calcium Binding Protein beta Subunit ; S100 Proteins - antagonists & inhibitors ; S100B ; Somesthesis and somesthetic pathways (proprioception, exteroception, nociception); interoception; electrolocation. Sensory receptors ; spinocerebellar ataxia type 1 ; Temperature ; thermal targeting ; Vertebrates: nervous system and sense organs</subject><ispartof>Neuroscience, 2011-12, Vol.197, p.369-380</ispartof><rights>IBRO</rights><rights>2011 IBRO</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2011 IBRO. Published by Elsevier Ltd. All rights reserved.</rights><rights>2011 IBRO. Published by Elsevier Ltd. All rights reserved. 2011</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c603t-5a99444563f594957e2efa281a45ee6e45ae049e3b0eb0c06f2f2dac1d1a9d943</citedby><cites>FETCH-LOGICAL-c603t-5a99444563f594957e2efa281a45ee6e45ae049e3b0eb0c06f2f2dac1d1a9d943</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0306452211010797$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24781783$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21958864$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hearst, S.M</creatorcontrib><creatorcontrib>Walker, L.R</creatorcontrib><creatorcontrib>Shao, Q</creatorcontrib><creatorcontrib>Lopez, M</creatorcontrib><creatorcontrib>Raucher, D</creatorcontrib><creatorcontrib>Vig, P.J.S</creatorcontrib><title>The design and delivery of a thermally responsive peptide to inhibit S100B-mediated neurodegeneration</title><title>Neuroscience</title><addtitle>Neuroscience</addtitle><description>Abstract S100B, a glial-secreted protein, is believed to play a major role in neurodegeneration in Alzheimer's disease, Down syndrome, traumatic brain injury, and spinocerebellar ataxia type 1 (SCA1). SCA1 is a trinucleotide repeat disorder in which the expanded polyglutamine mutation in the protein ataxin-1 primarily targets Purkinje cells of the cerebellum. Currently, the exact mechanism of S100B-mediated Purkinje cell damage in SCA1 is not clear. However, here we show that S100B may act via the activation of the receptor for advanced glycation end product (RAGE) signaling pathway, resulting in oxidative stress-mediated injury to mutant ataxin-1-expressing neurons. To combat S100B-mediated neurodegeneration, we have designed a selective thermally responsive S100B inhibitory peptide, Synb1-ELP-TRTK. Our therapeutic polypeptide was developed using three key elements: (1) the elastin-like polypeptide (ELP), a thermally responsive polypeptide, (2) the TRTK12 peptide, a known S100B inhibitory peptide, and (3) a cell-penetrating peptide, Synb1, to enhance intracellular delivery. Binding studies revealed that our peptide, Synb1-ELP-TRTK, interacts with its molecular target S100B and maintains a high S100B binding affinity as comparable with the TRTK12 peptide alone. In addition, in vitro studies revealed that Synb1-ELP-TRTK treatment reduces S100B uptake in SHSY5Y cells. Furthermore, the Synb1-ELP-TRTK peptide decreased S100B-induced oxidative damage to mutant ataxin-1-expressing neurons. To test the delivery capabilities of ELP-based therapeutic peptides to the cerebellum, we treated mice with fluorescently labeled Synb1-ELP and observed that thermal targeting enhanced peptide delivery to the cerebellum. Here, we have laid the framework for thermal-based therapeutic targeting to regions of the brain, particularly the cerebellum. Overall, our data suggest that thermal targeting of ELP-based therapeutic peptides to the cerebellum is a novel treatment strategy for cerebellar neurodegenerative disorders.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>CapZ Actin Capping Protein</subject><subject>Cell Line</subject><subject>cerebellum</subject><subject>Drug Design</subject><subject>elastin-like polypeptide</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>Immunoblotting</subject><subject>Mice</subject><subject>Nerve Degeneration - prevention & control</subject><subject>Nerve Growth Factors - antagonists & inhibitors</subject><subject>neurodegeneration</subject><subject>Neurology</subject><subject>Neuroprotective Agents - chemical synthesis</subject><subject>Neuroprotective Agents - metabolism</subject><subject>Neuroprotective Agents - pharmacology</subject><subject>Oligopeptides - metabolism</subject><subject>Oligopeptides - pharmacology</subject><subject>Peptide Fragments</subject><subject>Protein Binding - physiology</subject><subject>Proteins - metabolism</subject><subject>Proteins - pharmacology</subject><subject>S100 Calcium Binding Protein beta Subunit</subject><subject>S100 Proteins - antagonists & inhibitors</subject><subject>S100B</subject><subject>Somesthesis and somesthetic pathways (proprioception, exteroception, nociception); interoception; electrolocation. Sensory receptors</subject><subject>spinocerebellar ataxia type 1</subject><subject>Temperature</subject><subject>thermal targeting</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0306-4522</issn><issn>1873-7544</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkk2P0zAQhiMEYsvCX0AWEuKUMHbsJOaw0rJ8Sitx2OVsufakdUntYCeV-u9xaVkWLuCLLc0zM6_nnaJ4QaGiQJvXm8rjHEMyDr3BigGlFcgKmHhQLGjX1mUrOH9YLKCGpuSCsbPiSUobyEfw-nFxxqgUXdfwRYG3ayQWk1t5or3Nz8HtMO5J6Ikm0xrjVg_DnkRMY_Apx8iI4-QskikQ59du6SZyQwHellu0Tk9oyU95FlfoMerJBf-0eNTrIeGz031efP3w_vbqU3n95ePnq8vr0jRQT6XQUnLORVP3QnIpWmTYa9ZRzQVig1xoBC6xXgIuwUDTs55ZbailWlrJ6_Pi4lh3nJdZjUE_RT2oMbqtjnsVtFN_Rrxbq1XYqZpR4NDkAq9OBWL4PmOa1NYlg8OgPYY5KUkpFa1sxb9JYE0rKIVMvjmSJnuWIvZ3eiiog6Fqo-4bqg6GKpAqG5qTn9__0V3qLwcz8PIE6GT00EftjUu_Od52tO3qzL07cpjnv3MY1amddRHNpGxw_6fn4q8yZnDe5c7fcI9pE-bos8OKqsQUqJvDCh42MA-CQh5c_QPsPdyJ</recordid><startdate>20111201</startdate><enddate>20111201</enddate><creator>Hearst, S.M</creator><creator>Walker, L.R</creator><creator>Shao, Q</creator><creator>Lopez, M</creator><creator>Raucher, D</creator><creator>Vig, P.J.S</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>7X8</scope><scope>7TK</scope><scope>5PM</scope></search><sort><creationdate>20111201</creationdate><title>The design and delivery of a thermally responsive peptide to inhibit S100B-mediated neurodegeneration</title><author>Hearst, S.M ; Walker, L.R ; Shao, Q ; Lopez, M ; Raucher, D ; Vig, P.J.S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c603t-5a99444563f594957e2efa281a45ee6e45ae049e3b0eb0c06f2f2dac1d1a9d943</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>CapZ Actin Capping Protein</topic><topic>Cell Line</topic><topic>cerebellum</topic><topic>Drug Design</topic><topic>elastin-like polypeptide</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Humans</topic><topic>Immunoblotting</topic><topic>Mice</topic><topic>Nerve Degeneration - prevention & control</topic><topic>Nerve Growth Factors - antagonists & inhibitors</topic><topic>neurodegeneration</topic><topic>Neurology</topic><topic>Neuroprotective Agents - chemical synthesis</topic><topic>Neuroprotective Agents - metabolism</topic><topic>Neuroprotective Agents - pharmacology</topic><topic>Oligopeptides - metabolism</topic><topic>Oligopeptides - pharmacology</topic><topic>Peptide Fragments</topic><topic>Protein Binding - physiology</topic><topic>Proteins - metabolism</topic><topic>Proteins - pharmacology</topic><topic>S100 Calcium Binding Protein beta Subunit</topic><topic>S100 Proteins - antagonists & inhibitors</topic><topic>S100B</topic><topic>Somesthesis and somesthetic pathways (proprioception, exteroception, nociception); interoception; electrolocation. Sensory receptors</topic><topic>spinocerebellar ataxia type 1</topic><topic>Temperature</topic><topic>thermal targeting</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hearst, S.M</creatorcontrib><creatorcontrib>Walker, L.R</creatorcontrib><creatorcontrib>Shao, Q</creatorcontrib><creatorcontrib>Lopez, M</creatorcontrib><creatorcontrib>Raucher, D</creatorcontrib><creatorcontrib>Vig, P.J.S</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>MEDLINE - Academic</collection><collection>Neurosciences Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hearst, S.M</au><au>Walker, L.R</au><au>Shao, Q</au><au>Lopez, M</au><au>Raucher, D</au><au>Vig, P.J.S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The design and delivery of a thermally responsive peptide to inhibit S100B-mediated neurodegeneration</atitle><jtitle>Neuroscience</jtitle><addtitle>Neuroscience</addtitle><date>2011-12-01</date><risdate>2011</risdate><volume>197</volume><spage>369</spage><epage>380</epage><pages>369-380</pages><issn>0306-4522</issn><eissn>1873-7544</eissn><coden>NRSCDN</coden><abstract>Abstract S100B, a glial-secreted protein, is believed to play a major role in neurodegeneration in Alzheimer's disease, Down syndrome, traumatic brain injury, and spinocerebellar ataxia type 1 (SCA1). SCA1 is a trinucleotide repeat disorder in which the expanded polyglutamine mutation in the protein ataxin-1 primarily targets Purkinje cells of the cerebellum. Currently, the exact mechanism of S100B-mediated Purkinje cell damage in SCA1 is not clear. However, here we show that S100B may act via the activation of the receptor for advanced glycation end product (RAGE) signaling pathway, resulting in oxidative stress-mediated injury to mutant ataxin-1-expressing neurons. To combat S100B-mediated neurodegeneration, we have designed a selective thermally responsive S100B inhibitory peptide, Synb1-ELP-TRTK. Our therapeutic polypeptide was developed using three key elements: (1) the elastin-like polypeptide (ELP), a thermally responsive polypeptide, (2) the TRTK12 peptide, a known S100B inhibitory peptide, and (3) a cell-penetrating peptide, Synb1, to enhance intracellular delivery. Binding studies revealed that our peptide, Synb1-ELP-TRTK, interacts with its molecular target S100B and maintains a high S100B binding affinity as comparable with the TRTK12 peptide alone. In addition, in vitro studies revealed that Synb1-ELP-TRTK treatment reduces S100B uptake in SHSY5Y cells. Furthermore, the Synb1-ELP-TRTK peptide decreased S100B-induced oxidative damage to mutant ataxin-1-expressing neurons. To test the delivery capabilities of ELP-based therapeutic peptides to the cerebellum, we treated mice with fluorescently labeled Synb1-ELP and observed that thermal targeting enhanced peptide delivery to the cerebellum. Here, we have laid the framework for thermal-based therapeutic targeting to regions of the brain, particularly the cerebellum. Overall, our data suggest that thermal targeting of ELP-based therapeutic peptides to the cerebellum is a novel treatment strategy for cerebellar neurodegenerative disorders.</abstract><cop>Amsterdam</cop><pub>Elsevier Ltd</pub><pmid>21958864</pmid><doi>10.1016/j.neuroscience.2011.09.025</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Biological and medical sciences CapZ Actin Capping Protein Cell Line cerebellum Drug Design elastin-like polypeptide Fundamental and applied biological sciences. Psychology Humans Immunoblotting Mice Nerve Degeneration - prevention & control Nerve Growth Factors - antagonists & inhibitors neurodegeneration Neurology Neuroprotective Agents - chemical synthesis Neuroprotective Agents - metabolism Neuroprotective Agents - pharmacology Oligopeptides - metabolism Oligopeptides - pharmacology Peptide Fragments Protein Binding - physiology Proteins - metabolism Proteins - pharmacology S100 Calcium Binding Protein beta Subunit S100 Proteins - antagonists & inhibitors S100B Somesthesis and somesthetic pathways (proprioception, exteroception, nociception) interoception electrolocation. Sensory receptors spinocerebellar ataxia type 1 Temperature thermal targeting Vertebrates: nervous system and sense organs |
title | The design and delivery of a thermally responsive peptide to inhibit S100B-mediated neurodegeneration |
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