Enhancing the hypotensive effect and diminishing the cytolytic activity of hornet mastoparan B by D-amino acid substitution
Mastoparan B (MP-B) is a cationic tetradecapeptide (LKLKSIVSWAKKVL-CONH 2) isolated from the venom of the Taiwan hornet Vespa basalis. Unlike other vespid mastoparans, the peptide is capable of inducing short-term hypotension and causes hemolysis in animals. This study was aimed to find out MP-B ana...
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description | Mastoparan B (MP-B) is a cationic tetradecapeptide (LKLKSIVSWAKKVL-CONH
2) isolated from the venom of the Taiwan hornet
Vespa basalis. Unlike other vespid mastoparans, the peptide is capable of inducing short-term hypotension and causes hemolysis in animals. This study was aimed to find out MP-B analogs that possess higher hypotensive potency with the least lytic action by D-amino acid substitution, especially at lysine (Lys) residues. The synthetic MP-B isomer in which Lys
2 was replaced by D-Lys showed a significant decrease in both hemolytic and hypotensive activities. Substitution of Lys
4 by D-Lys in MP-B also caused a marked reduction of hemolytic activity, but its hypotensive action was only slightly affected. However, when Lys
11,12 were replaced by D-Lys, the resulting isomer ([D-Lys
11,12]MP-B) exhibited a higher hypotensive activity with negligible hemolytic activity as compared with the native peptide. The D-antipot of MP-B in which all amino acid residues were replaced by D-isomers showed the highest hypotensive activity with a hemolytic activity about 1/5 that of MP-B. The results reveal that D-Lys substitution at the N-terminus of MP-B (Lys
2,4) causes decreases in both hypotensive and hemolytic activities, while D-Lys substitution at the C-terminus (Lys
11,12) leads to a significant increase in hypotensive activity of MP-B with a remarkable decrease in hemolytic activity. The hypotensive effect of [D-Lys
11,12]MP-B was more prominent on spontaneously hypertensive rats. At a proper dose (0.3
mg/kg) the peptide could reduce the high blood pressure (~180
mm
Hg) of the rat to a normal level (~120
mm
Hg) for more than 3
h. [D-Lys
11,12]MP-B which possesses a potent hypotensive action with the least cytolytic side effect is the best MP-B analog for studying the mechanism of cardiovascular inhibition by MP-B and could be useful as a hypotensive agent in hypertension crisis. |
doi_str_mv | 10.1016/S0041-0101(01)00128-3 |
format | Article |
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2) isolated from the venom of the Taiwan hornet
Vespa basalis. Unlike other vespid mastoparans, the peptide is capable of inducing short-term hypotension and causes hemolysis in animals. This study was aimed to find out MP-B analogs that possess higher hypotensive potency with the least lytic action by D-amino acid substitution, especially at lysine (Lys) residues. The synthetic MP-B isomer in which Lys
2 was replaced by D-Lys showed a significant decrease in both hemolytic and hypotensive activities. Substitution of Lys
4 by D-Lys in MP-B also caused a marked reduction of hemolytic activity, but its hypotensive action was only slightly affected. However, when Lys
11,12 were replaced by D-Lys, the resulting isomer ([D-Lys
11,12]MP-B) exhibited a higher hypotensive activity with negligible hemolytic activity as compared with the native peptide. The D-antipot of MP-B in which all amino acid residues were replaced by D-isomers showed the highest hypotensive activity with a hemolytic activity about 1/5 that of MP-B. The results reveal that D-Lys substitution at the N-terminus of MP-B (Lys
2,4) causes decreases in both hypotensive and hemolytic activities, while D-Lys substitution at the C-terminus (Lys
11,12) leads to a significant increase in hypotensive activity of MP-B with a remarkable decrease in hemolytic activity. The hypotensive effect of [D-Lys
11,12]MP-B was more prominent on spontaneously hypertensive rats. At a proper dose (0.3
mg/kg) the peptide could reduce the high blood pressure (~180
mm
Hg) of the rat to a normal level (~120
mm
Hg) for more than 3
h. [D-Lys
11,12]MP-B which possesses a potent hypotensive action with the least cytolytic side effect is the best MP-B analog for studying the mechanism of cardiovascular inhibition by MP-B and could be useful as a hypotensive agent in hypertension crisis.</description><identifier>ISSN: 0041-0101</identifier><identifier>EISSN: 1879-3150</identifier><identifier>DOI: 10.1016/S0041-0101(01)00128-3</identifier><identifier>PMID: 11478963</identifier><identifier>CODEN: TOXIA6</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Amino Acid Sequence ; Amino Acid Substitution ; Animal poisons toxicology. Antivenoms ; Animals ; Biological and medical sciences ; Blood Pressure - physiology ; Chromatography, High Pressure Liquid ; Circular Dichroism ; Dose-Response Relationship, Drug ; Erythrocytes - drug effects ; Guinea Pigs ; Hemolysis - drug effects ; Hypotension - drug therapy ; lysine ; Lysine - chemistry ; Male ; mastoparan ; mastoparan B ; Medical sciences ; Peptides - chemical synthesis ; Peptides - chemistry ; Peptides - isolation & purification ; Peptides - physiology ; Rats ; Rats, Inbred SHR ; Rats, Wistar ; Stereoisomerism ; Structure-Activity Relationship ; Time Factors ; Toxicology ; Vespa basalis ; Vespidae ; Wasp Venoms - chemistry ; Wasp Venoms - isolation & purification ; Wasps</subject><ispartof>Toxicon (Oxford), 2001-10, Vol.39 (10), p.1561-1566</ispartof><rights>2001 Elsevier Science Ltd</rights><rights>2001 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c421t-5fe13970f4968231a557a1ecc0cb53eb28d9bdbc12cdf7dc2669483a615bad243</citedby><cites>FETCH-LOGICAL-c421t-5fe13970f4968231a557a1ecc0cb53eb28d9bdbc12cdf7dc2669483a615bad243</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0041010101001283$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1077734$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11478963$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ho, Chewn-Lang</creatorcontrib><creatorcontrib>Shih, Yan-Ping</creatorcontrib><creatorcontrib>Wang, Kung-Tsung</creatorcontrib><creatorcontrib>Yu, Hui-Ming</creatorcontrib><title>Enhancing the hypotensive effect and diminishing the cytolytic activity of hornet mastoparan B by D-amino acid substitution</title><title>Toxicon (Oxford)</title><addtitle>Toxicon</addtitle><description>Mastoparan B (MP-B) is a cationic tetradecapeptide (LKLKSIVSWAKKVL-CONH
2) isolated from the venom of the Taiwan hornet
Vespa basalis. Unlike other vespid mastoparans, the peptide is capable of inducing short-term hypotension and causes hemolysis in animals. This study was aimed to find out MP-B analogs that possess higher hypotensive potency with the least lytic action by D-amino acid substitution, especially at lysine (Lys) residues. The synthetic MP-B isomer in which Lys
2 was replaced by D-Lys showed a significant decrease in both hemolytic and hypotensive activities. Substitution of Lys
4 by D-Lys in MP-B also caused a marked reduction of hemolytic activity, but its hypotensive action was only slightly affected. However, when Lys
11,12 were replaced by D-Lys, the resulting isomer ([D-Lys
11,12]MP-B) exhibited a higher hypotensive activity with negligible hemolytic activity as compared with the native peptide. The D-antipot of MP-B in which all amino acid residues were replaced by D-isomers showed the highest hypotensive activity with a hemolytic activity about 1/5 that of MP-B. The results reveal that D-Lys substitution at the N-terminus of MP-B (Lys
2,4) causes decreases in both hypotensive and hemolytic activities, while D-Lys substitution at the C-terminus (Lys
11,12) leads to a significant increase in hypotensive activity of MP-B with a remarkable decrease in hemolytic activity. The hypotensive effect of [D-Lys
11,12]MP-B was more prominent on spontaneously hypertensive rats. At a proper dose (0.3
mg/kg) the peptide could reduce the high blood pressure (~180
mm
Hg) of the rat to a normal level (~120
mm
Hg) for more than 3
h. [D-Lys
11,12]MP-B which possesses a potent hypotensive action with the least cytolytic side effect is the best MP-B analog for studying the mechanism of cardiovascular inhibition by MP-B and could be useful as a hypotensive agent in hypertension crisis.</description><subject>Amino Acid Sequence</subject><subject>Amino Acid Substitution</subject><subject>Animal poisons toxicology. Antivenoms</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Blood Pressure - physiology</subject><subject>Chromatography, High Pressure Liquid</subject><subject>Circular Dichroism</subject><subject>Dose-Response Relationship, Drug</subject><subject>Erythrocytes - drug effects</subject><subject>Guinea Pigs</subject><subject>Hemolysis - drug effects</subject><subject>Hypotension - drug therapy</subject><subject>lysine</subject><subject>Lysine - chemistry</subject><subject>Male</subject><subject>mastoparan</subject><subject>mastoparan B</subject><subject>Medical sciences</subject><subject>Peptides - chemical synthesis</subject><subject>Peptides - chemistry</subject><subject>Peptides - isolation & purification</subject><subject>Peptides - physiology</subject><subject>Rats</subject><subject>Rats, Inbred SHR</subject><subject>Rats, Wistar</subject><subject>Stereoisomerism</subject><subject>Structure-Activity Relationship</subject><subject>Time Factors</subject><subject>Toxicology</subject><subject>Vespa basalis</subject><subject>Vespidae</subject><subject>Wasp Venoms - chemistry</subject><subject>Wasp Venoms - isolation & purification</subject><subject>Wasps</subject><issn>0041-0101</issn><issn>1879-3150</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1v1DAQhi0EotvCTwD5gFA5BDxxEienCkr5kCpxAM6WY0-IUWIvtrNSxJ_HYZePWyVLnsMz4_H7EPIE2Etg0Lz6zFgFBcv1JYMXjEHZFvwe2UEruoJDze6T3V_kjJzH-J0xxtuueUjOACqRK74jP2_cqJy27htNI9Jx3fuELtoDUhwG1IkqZ6ixs3U2jn8wvSY_rclqqnSyB5tW6gc6-uAw0VnF5PcqKEff0H6lbwuVu31GraFx6WOyaUnWu0fkwaCmiI9P9wX5-u7my_WH4vbT-4_Xr28LXZWQinpA4J1gQ9U1bclB1bVQgFoz3dcc-7I1XW96DaU2gzC6bJquarlqoO6VKSt-QZ4f5-6D_7FgTHK2UeM0KYd-iVIAq3grmjtBaKHM-bYZrI-gDj7GgIPcBzursEpgctMjf-uRW_ZyO5seyXPf09MDSz-j-dd18pGBZydARa2mIWxu4n_ThRB8-9HVEcMc28FikFFbdBqNDdmZNN7esckvCJatpg</recordid><startdate>20011001</startdate><enddate>20011001</enddate><creator>Ho, Chewn-Lang</creator><creator>Shih, Yan-Ping</creator><creator>Wang, Kung-Tsung</creator><creator>Yu, Hui-Ming</creator><general>Elsevier Ltd</general><general>Elsevier Science</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>7SS</scope><scope>7U7</scope><scope>C1K</scope><scope>7X8</scope></search><sort><creationdate>20011001</creationdate><title>Enhancing the hypotensive effect and diminishing the cytolytic activity of hornet mastoparan B by D-amino acid substitution</title><author>Ho, Chewn-Lang ; Shih, Yan-Ping ; Wang, Kung-Tsung ; Yu, Hui-Ming</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c421t-5fe13970f4968231a557a1ecc0cb53eb28d9bdbc12cdf7dc2669483a615bad243</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>Amino Acid Sequence</topic><topic>Amino Acid Substitution</topic><topic>Animal poisons toxicology. Antivenoms</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Blood Pressure - physiology</topic><topic>Chromatography, High Pressure Liquid</topic><topic>Circular Dichroism</topic><topic>Dose-Response Relationship, Drug</topic><topic>Erythrocytes - drug effects</topic><topic>Guinea Pigs</topic><topic>Hemolysis - drug effects</topic><topic>Hypotension - drug therapy</topic><topic>lysine</topic><topic>Lysine - chemistry</topic><topic>Male</topic><topic>mastoparan</topic><topic>mastoparan B</topic><topic>Medical sciences</topic><topic>Peptides - chemical synthesis</topic><topic>Peptides - chemistry</topic><topic>Peptides - isolation & purification</topic><topic>Peptides - physiology</topic><topic>Rats</topic><topic>Rats, Inbred SHR</topic><topic>Rats, Wistar</topic><topic>Stereoisomerism</topic><topic>Structure-Activity Relationship</topic><topic>Time Factors</topic><topic>Toxicology</topic><topic>Vespa basalis</topic><topic>Vespidae</topic><topic>Wasp Venoms - chemistry</topic><topic>Wasp Venoms - isolation & purification</topic><topic>Wasps</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ho, Chewn-Lang</creatorcontrib><creatorcontrib>Shih, Yan-Ping</creatorcontrib><creatorcontrib>Wang, Kung-Tsung</creatorcontrib><creatorcontrib>Yu, Hui-Ming</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>Entomology Abstracts (Full archive)</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><jtitle>Toxicon (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ho, Chewn-Lang</au><au>Shih, Yan-Ping</au><au>Wang, Kung-Tsung</au><au>Yu, Hui-Ming</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Enhancing the hypotensive effect and diminishing the cytolytic activity of hornet mastoparan B by D-amino acid substitution</atitle><jtitle>Toxicon (Oxford)</jtitle><addtitle>Toxicon</addtitle><date>2001-10-01</date><risdate>2001</risdate><volume>39</volume><issue>10</issue><spage>1561</spage><epage>1566</epage><pages>1561-1566</pages><issn>0041-0101</issn><eissn>1879-3150</eissn><coden>TOXIA6</coden><abstract>Mastoparan B (MP-B) is a cationic tetradecapeptide (LKLKSIVSWAKKVL-CONH
2) isolated from the venom of the Taiwan hornet
Vespa basalis. Unlike other vespid mastoparans, the peptide is capable of inducing short-term hypotension and causes hemolysis in animals. This study was aimed to find out MP-B analogs that possess higher hypotensive potency with the least lytic action by D-amino acid substitution, especially at lysine (Lys) residues. The synthetic MP-B isomer in which Lys
2 was replaced by D-Lys showed a significant decrease in both hemolytic and hypotensive activities. Substitution of Lys
4 by D-Lys in MP-B also caused a marked reduction of hemolytic activity, but its hypotensive action was only slightly affected. However, when Lys
11,12 were replaced by D-Lys, the resulting isomer ([D-Lys
11,12]MP-B) exhibited a higher hypotensive activity with negligible hemolytic activity as compared with the native peptide. The D-antipot of MP-B in which all amino acid residues were replaced by D-isomers showed the highest hypotensive activity with a hemolytic activity about 1/5 that of MP-B. The results reveal that D-Lys substitution at the N-terminus of MP-B (Lys
2,4) causes decreases in both hypotensive and hemolytic activities, while D-Lys substitution at the C-terminus (Lys
11,12) leads to a significant increase in hypotensive activity of MP-B with a remarkable decrease in hemolytic activity. The hypotensive effect of [D-Lys
11,12]MP-B was more prominent on spontaneously hypertensive rats. At a proper dose (0.3
mg/kg) the peptide could reduce the high blood pressure (~180
mm
Hg) of the rat to a normal level (~120
mm
Hg) for more than 3
h. [D-Lys
11,12]MP-B which possesses a potent hypotensive action with the least cytolytic side effect is the best MP-B analog for studying the mechanism of cardiovascular inhibition by MP-B and could be useful as a hypotensive agent in hypertension crisis.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>11478963</pmid><doi>10.1016/S0041-0101(01)00128-3</doi><tpages>6</tpages></addata></record> |
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source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | Amino Acid Sequence Amino Acid Substitution Animal poisons toxicology. Antivenoms Animals Biological and medical sciences Blood Pressure - physiology Chromatography, High Pressure Liquid Circular Dichroism Dose-Response Relationship, Drug Erythrocytes - drug effects Guinea Pigs Hemolysis - drug effects Hypotension - drug therapy lysine Lysine - chemistry Male mastoparan mastoparan B Medical sciences Peptides - chemical synthesis Peptides - chemistry Peptides - isolation & purification Peptides - physiology Rats Rats, Inbred SHR Rats, Wistar Stereoisomerism Structure-Activity Relationship Time Factors Toxicology Vespa basalis Vespidae Wasp Venoms - chemistry Wasp Venoms - isolation & purification Wasps |
title | Enhancing the hypotensive effect and diminishing the cytolytic activity of hornet mastoparan B by D-amino acid substitution |
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