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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Veröffentlicht in:Toxicon (Oxford) 2001-10, Vol.39 (10), p.1561-1566
Hauptverfasser: Ho, Chewn-Lang, Shih, Yan-Ping, Wang, Kung-Tsung, Yu, Hui-Ming
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Shih, Yan-Ping
Wang, Kung-Tsung
Yu, Hui-Ming
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
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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. 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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 &amp; 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 &amp; 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 &amp; 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 &amp; 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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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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