Characterization of Poly-Leucine Substituted Analogues of the Human Surfactant Protein SP-C

A series of novel amphipathic peptides constituted of an N-terminal hydrophilic portion (CPVHLKR, residues 6-12) of human pulmonary surfactant protein-C (SP-C) and a poly-leucine (poly-L) stretch of various chain lengths as the C-terminal hydrophobic tail were synthesized and evaluated relevant to t...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Biological & pharmaceutical bulletin 1996/12/15, Vol.19(12), pp.1550-1555
Hauptverfasser: TAKEI, Tsunetomo, HASHIMOTO, Yohichi, OHTSUBO, Eiji, SAKAI, Kaoru, OHKAWA, Hiroshi
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1555
container_issue 12
container_start_page 1550
container_title Biological & pharmaceutical bulletin
container_volume 19
creator TAKEI, Tsunetomo
HASHIMOTO, Yohichi
OHTSUBO, Eiji
SAKAI, Kaoru
OHKAWA, Hiroshi
description A series of novel amphipathic peptides constituted of an N-terminal hydrophilic portion (CPVHLKR, residues 6-12) of human pulmonary surfactant protein-C (SP-C) and a poly-leucine (poly-L) stretch of various chain lengths as the C-terminal hydrophobic tail were synthesized and evaluated relevant to their ability to improve the surface activity of a ternary lipid mixture composed of dipalmitoylphosphatidylcholine, egg-phosphatidylglycerol and palmitic acid (DPPC/E-PG/PA, 75 : 25 : 10, w/w) in a Langmuir-Wilhelmy surface balance. CPVHLKRL11, a human SP-C analogue bearing an 11-residue poly-L tail, and its related peptides with longer tails in the ternary lipid mixture, accelerated not only the surface spreading at the air-water interface but also exhibited significantly improved dynamic surface activity, compared to the ternary lipid mixture. Their surface activities were almost indiscernible from those of the synthetic human SP-C. When reconstituted into a ternary lipid mixture containing members of the homologous series of n-saturated diacylphosphatidylglycerol, the surface activities of the poly-L analogues were almost completely unaffected, whereas replica peptides carrying the hydrophobic portion of native SP-C were found to have distinct surface activities depending upon the acyl-chain lengths of phosphatidylglycerol. The poly-L stretch of a poly-L analogue could be replaced with poly-norleucine of the same chain length without a significant loss of surface activity.Substitution of the poly-L portion in the analogues with poly-valine or poly-isoleucine resulted in a considerable decrease in surface activity. The poly-L analogue in the DPPC/E-PG/PA mixture was demonstrated to act as an excellent surfactant comparable with Surfactan[○!R], a modified bovine surfactant preparation that was used for treatment for infant respiratory distress syndrome, based on evaluation of the lung pressure-volume characteristics using premature rabbit neonates.
doi_str_mv 10.1248/bpb.19.1550
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_78659217</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3120325061</sourcerecordid><originalsourceid>FETCH-LOGICAL-c507t-5d3fb40a8ecf57e720dbc8aaf9d7f4de2aaadaad361dc0fa553b83ff6a411ac3</originalsourceid><addsrcrecordid>eNpdkc9rFDEcxYModa2ePAsDiheZbX5OkmNZrC0suNDePITvZJI2y-xkTTKH-tebddc9FEICeR_e--YFoY8ELwnl6qrf90uil0QI_AotCOOyFZSI12iBNVFtR4R6i97lvMUYS0zZBbpQWncdkwv0a_UECWxxKfyBEuLURN9s4vjcrt1sw-Sa-7nPJZS5uKG5nmCMj7PLB6o8ueZ23sFUkeSrB0yl2aRYXKhXm3b1Hr3xMGb34XReooeb7w-r23b988fd6nrdWoFlacXAfM8xKGe9kE5SPPRWAXg9SM8HRwFgqIt1ZLDYgxCsV8z7DjghYNkl-nq03af4u85WzC5k68YRJhfnbKTqhKZEVvDzC3Ab51SflA3hXJOOao4r9e1I2RRzTs6bfQo7SM-GYHPo29S-DdHm0HelP508537nhjN7KrjqX046ZAujTzDZkM8YFVJxxSp2c8S2ucCjO-uQSrCjO0QSrdm_WPp_r_lnwNZvNG5ifwFcE6Gt</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1449162940</pqid></control><display><type>article</type><title>Characterization of Poly-Leucine Substituted Analogues of the Human Surfactant Protein SP-C</title><source>J-STAGE Free</source><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Free Full-Text Journals in Chemistry</source><creator>TAKEI, Tsunetomo ; HASHIMOTO, Yohichi ; OHTSUBO, Eiji ; SAKAI, Kaoru ; OHKAWA, Hiroshi</creator><creatorcontrib>TAKEI, Tsunetomo ; HASHIMOTO, Yohichi ; OHTSUBO, Eiji ; SAKAI, Kaoru ; OHKAWA, Hiroshi</creatorcontrib><description>A series of novel amphipathic peptides constituted of an N-terminal hydrophilic portion (CPVHLKR, residues 6-12) of human pulmonary surfactant protein-C (SP-C) and a poly-leucine (poly-L) stretch of various chain lengths as the C-terminal hydrophobic tail were synthesized and evaluated relevant to their ability to improve the surface activity of a ternary lipid mixture composed of dipalmitoylphosphatidylcholine, egg-phosphatidylglycerol and palmitic acid (DPPC/E-PG/PA, 75 : 25 : 10, w/w) in a Langmuir-Wilhelmy surface balance. CPVHLKRL11, a human SP-C analogue bearing an 11-residue poly-L tail, and its related peptides with longer tails in the ternary lipid mixture, accelerated not only the surface spreading at the air-water interface but also exhibited significantly improved dynamic surface activity, compared to the ternary lipid mixture. Their surface activities were almost indiscernible from those of the synthetic human SP-C. When reconstituted into a ternary lipid mixture containing members of the homologous series of n-saturated diacylphosphatidylglycerol, the surface activities of the poly-L analogues were almost completely unaffected, whereas replica peptides carrying the hydrophobic portion of native SP-C were found to have distinct surface activities depending upon the acyl-chain lengths of phosphatidylglycerol. The poly-L stretch of a poly-L analogue could be replaced with poly-norleucine of the same chain length without a significant loss of surface activity.Substitution of the poly-L portion in the analogues with poly-valine or poly-isoleucine resulted in a considerable decrease in surface activity. The poly-L analogue in the DPPC/E-PG/PA mixture was demonstrated to act as an excellent surfactant comparable with Surfactan[○!R], a modified bovine surfactant preparation that was used for treatment for infant respiratory distress syndrome, based on evaluation of the lung pressure-volume characteristics using premature rabbit neonates.</description><identifier>ISSN: 0918-6158</identifier><identifier>EISSN: 1347-5215</identifier><identifier>DOI: 10.1248/bpb.19.1550</identifier><identifier>PMID: 8996637</identifier><language>eng</language><publisher>Tokyo: The Pharmaceutical Society of Japan</publisher><subject>Amino Acid Sequence ; Animals ; Biological and medical sciences ; Biophysical Phenomena ; Biophysics ; Chemical Phenomena ; Chemistry, Physical ; Diseases of the respiratory system ; Female ; Humans ; Lipids - chemistry ; Medical sciences ; Molecular Sequence Data ; Peptides - chemical synthesis ; Peptides - chemistry ; poly-leucine substituted analogue ; Pregnancy ; Proteolipids - chemical synthesis ; Proteolipids - chemistry ; pulmonary surfactant ; Pulmonary Surfactants - chemical synthesis ; Pulmonary Surfactants - chemistry ; Rabbits ; Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects) ; surface activity ; Surface-Active Agents - chemical synthesis ; Surface-Active Agents - chemistry ; surfactant protein-C (SP-C) ; synthetic peptide</subject><ispartof>Biological and Pharmaceutical Bulletin, 1996/12/15, Vol.19(12), pp.1550-1555</ispartof><rights>The Pharmaceutical Society of Japan</rights><rights>1997 INIST-CNRS</rights><rights>Copyright Japan Science and Technology Agency 1996</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c507t-5d3fb40a8ecf57e720dbc8aaf9d7f4de2aaadaad361dc0fa553b83ff6a411ac3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,1884,27929,27930</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=2578483$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8996637$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>TAKEI, Tsunetomo</creatorcontrib><creatorcontrib>HASHIMOTO, Yohichi</creatorcontrib><creatorcontrib>OHTSUBO, Eiji</creatorcontrib><creatorcontrib>SAKAI, Kaoru</creatorcontrib><creatorcontrib>OHKAWA, Hiroshi</creatorcontrib><title>Characterization of Poly-Leucine Substituted Analogues of the Human Surfactant Protein SP-C</title><title>Biological &amp; pharmaceutical bulletin</title><addtitle>Biol Pharm Bull</addtitle><description>A series of novel amphipathic peptides constituted of an N-terminal hydrophilic portion (CPVHLKR, residues 6-12) of human pulmonary surfactant protein-C (SP-C) and a poly-leucine (poly-L) stretch of various chain lengths as the C-terminal hydrophobic tail were synthesized and evaluated relevant to their ability to improve the surface activity of a ternary lipid mixture composed of dipalmitoylphosphatidylcholine, egg-phosphatidylglycerol and palmitic acid (DPPC/E-PG/PA, 75 : 25 : 10, w/w) in a Langmuir-Wilhelmy surface balance. CPVHLKRL11, a human SP-C analogue bearing an 11-residue poly-L tail, and its related peptides with longer tails in the ternary lipid mixture, accelerated not only the surface spreading at the air-water interface but also exhibited significantly improved dynamic surface activity, compared to the ternary lipid mixture. Their surface activities were almost indiscernible from those of the synthetic human SP-C. When reconstituted into a ternary lipid mixture containing members of the homologous series of n-saturated diacylphosphatidylglycerol, the surface activities of the poly-L analogues were almost completely unaffected, whereas replica peptides carrying the hydrophobic portion of native SP-C were found to have distinct surface activities depending upon the acyl-chain lengths of phosphatidylglycerol. The poly-L stretch of a poly-L analogue could be replaced with poly-norleucine of the same chain length without a significant loss of surface activity.Substitution of the poly-L portion in the analogues with poly-valine or poly-isoleucine resulted in a considerable decrease in surface activity. The poly-L analogue in the DPPC/E-PG/PA mixture was demonstrated to act as an excellent surfactant comparable with Surfactan[○!R], a modified bovine surfactant preparation that was used for treatment for infant respiratory distress syndrome, based on evaluation of the lung pressure-volume characteristics using premature rabbit neonates.</description><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Biophysical Phenomena</subject><subject>Biophysics</subject><subject>Chemical Phenomena</subject><subject>Chemistry, Physical</subject><subject>Diseases of the respiratory system</subject><subject>Female</subject><subject>Humans</subject><subject>Lipids - chemistry</subject><subject>Medical sciences</subject><subject>Molecular Sequence Data</subject><subject>Peptides - chemical synthesis</subject><subject>Peptides - chemistry</subject><subject>poly-leucine substituted analogue</subject><subject>Pregnancy</subject><subject>Proteolipids - chemical synthesis</subject><subject>Proteolipids - chemistry</subject><subject>pulmonary surfactant</subject><subject>Pulmonary Surfactants - chemical synthesis</subject><subject>Pulmonary Surfactants - chemistry</subject><subject>Rabbits</subject><subject>Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects)</subject><subject>surface activity</subject><subject>Surface-Active Agents - chemical synthesis</subject><subject>Surface-Active Agents - chemistry</subject><subject>surfactant protein-C (SP-C)</subject><subject>synthetic peptide</subject><issn>0918-6158</issn><issn>1347-5215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkc9rFDEcxYModa2ePAsDiheZbX5OkmNZrC0suNDePITvZJI2y-xkTTKH-tebddc9FEICeR_e--YFoY8ELwnl6qrf90uil0QI_AotCOOyFZSI12iBNVFtR4R6i97lvMUYS0zZBbpQWncdkwv0a_UECWxxKfyBEuLURN9s4vjcrt1sw-Sa-7nPJZS5uKG5nmCMj7PLB6o8ueZ23sFUkeSrB0yl2aRYXKhXm3b1Hr3xMGb34XReooeb7w-r23b988fd6nrdWoFlacXAfM8xKGe9kE5SPPRWAXg9SM8HRwFgqIt1ZLDYgxCsV8z7DjghYNkl-nq03af4u85WzC5k68YRJhfnbKTqhKZEVvDzC3Ab51SflA3hXJOOao4r9e1I2RRzTs6bfQo7SM-GYHPo29S-DdHm0HelP508537nhjN7KrjqX046ZAujTzDZkM8YFVJxxSp2c8S2ucCjO-uQSrCjO0QSrdm_WPp_r_lnwNZvNG5ifwFcE6Gt</recordid><startdate>19961201</startdate><enddate>19961201</enddate><creator>TAKEI, Tsunetomo</creator><creator>HASHIMOTO, Yohichi</creator><creator>OHTSUBO, Eiji</creator><creator>SAKAI, Kaoru</creator><creator>OHKAWA, Hiroshi</creator><general>The Pharmaceutical Society of Japan</general><general>Maruzen</general><general>Japan Science and Technology Agency</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>7QR</scope><scope>7TK</scope><scope>7U9</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>19961201</creationdate><title>Characterization of Poly-Leucine Substituted Analogues of the Human Surfactant Protein SP-C</title><author>TAKEI, Tsunetomo ; HASHIMOTO, Yohichi ; OHTSUBO, Eiji ; SAKAI, Kaoru ; OHKAWA, Hiroshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c507t-5d3fb40a8ecf57e720dbc8aaf9d7f4de2aaadaad361dc0fa553b83ff6a411ac3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Biophysical Phenomena</topic><topic>Biophysics</topic><topic>Chemical Phenomena</topic><topic>Chemistry, Physical</topic><topic>Diseases of the respiratory system</topic><topic>Female</topic><topic>Humans</topic><topic>Lipids - chemistry</topic><topic>Medical sciences</topic><topic>Molecular Sequence Data</topic><topic>Peptides - chemical synthesis</topic><topic>Peptides - chemistry</topic><topic>poly-leucine substituted analogue</topic><topic>Pregnancy</topic><topic>Proteolipids - chemical synthesis</topic><topic>Proteolipids - chemistry</topic><topic>pulmonary surfactant</topic><topic>Pulmonary Surfactants - chemical synthesis</topic><topic>Pulmonary Surfactants - chemistry</topic><topic>Rabbits</topic><topic>Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects)</topic><topic>surface activity</topic><topic>Surface-Active Agents - chemical synthesis</topic><topic>Surface-Active Agents - chemistry</topic><topic>surfactant protein-C (SP-C)</topic><topic>synthetic peptide</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>TAKEI, Tsunetomo</creatorcontrib><creatorcontrib>HASHIMOTO, Yohichi</creatorcontrib><creatorcontrib>OHTSUBO, Eiji</creatorcontrib><creatorcontrib>SAKAI, Kaoru</creatorcontrib><creatorcontrib>OHKAWA, Hiroshi</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 &amp; Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Biological &amp; pharmaceutical bulletin</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>TAKEI, Tsunetomo</au><au>HASHIMOTO, Yohichi</au><au>OHTSUBO, Eiji</au><au>SAKAI, Kaoru</au><au>OHKAWA, Hiroshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Characterization of Poly-Leucine Substituted Analogues of the Human Surfactant Protein SP-C</atitle><jtitle>Biological &amp; pharmaceutical bulletin</jtitle><addtitle>Biol Pharm Bull</addtitle><date>1996-12-01</date><risdate>1996</risdate><volume>19</volume><issue>12</issue><spage>1550</spage><epage>1555</epage><pages>1550-1555</pages><issn>0918-6158</issn><eissn>1347-5215</eissn><abstract>A series of novel amphipathic peptides constituted of an N-terminal hydrophilic portion (CPVHLKR, residues 6-12) of human pulmonary surfactant protein-C (SP-C) and a poly-leucine (poly-L) stretch of various chain lengths as the C-terminal hydrophobic tail were synthesized and evaluated relevant to their ability to improve the surface activity of a ternary lipid mixture composed of dipalmitoylphosphatidylcholine, egg-phosphatidylglycerol and palmitic acid (DPPC/E-PG/PA, 75 : 25 : 10, w/w) in a Langmuir-Wilhelmy surface balance. CPVHLKRL11, a human SP-C analogue bearing an 11-residue poly-L tail, and its related peptides with longer tails in the ternary lipid mixture, accelerated not only the surface spreading at the air-water interface but also exhibited significantly improved dynamic surface activity, compared to the ternary lipid mixture. Their surface activities were almost indiscernible from those of the synthetic human SP-C. When reconstituted into a ternary lipid mixture containing members of the homologous series of n-saturated diacylphosphatidylglycerol, the surface activities of the poly-L analogues were almost completely unaffected, whereas replica peptides carrying the hydrophobic portion of native SP-C were found to have distinct surface activities depending upon the acyl-chain lengths of phosphatidylglycerol. The poly-L stretch of a poly-L analogue could be replaced with poly-norleucine of the same chain length without a significant loss of surface activity.Substitution of the poly-L portion in the analogues with poly-valine or poly-isoleucine resulted in a considerable decrease in surface activity. The poly-L analogue in the DPPC/E-PG/PA mixture was demonstrated to act as an excellent surfactant comparable with Surfactan[○!R], a modified bovine surfactant preparation that was used for treatment for infant respiratory distress syndrome, based on evaluation of the lung pressure-volume characteristics using premature rabbit neonates.</abstract><cop>Tokyo</cop><pub>The Pharmaceutical Society of Japan</pub><pmid>8996637</pmid><doi>10.1248/bpb.19.1550</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0918-6158
ispartof Biological and Pharmaceutical Bulletin, 1996/12/15, Vol.19(12), pp.1550-1555
issn 0918-6158
1347-5215
language eng
recordid cdi_proquest_miscellaneous_78659217
source J-STAGE Free; MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Free Full-Text Journals in Chemistry
subjects Amino Acid Sequence
Animals
Biological and medical sciences
Biophysical Phenomena
Biophysics
Chemical Phenomena
Chemistry, Physical
Diseases of the respiratory system
Female
Humans
Lipids - chemistry
Medical sciences
Molecular Sequence Data
Peptides - chemical synthesis
Peptides - chemistry
poly-leucine substituted analogue
Pregnancy
Proteolipids - chemical synthesis
Proteolipids - chemistry
pulmonary surfactant
Pulmonary Surfactants - chemical synthesis
Pulmonary Surfactants - chemistry
Rabbits
Radiotherapy. Instrumental treatment. Physiotherapy. Reeducation. Rehabilitation, orthophony, crenotherapy. Diet therapy and various other treatments (general aspects)
surface activity
Surface-Active Agents - chemical synthesis
Surface-Active Agents - chemistry
surfactant protein-C (SP-C)
synthetic peptide
title Characterization of Poly-Leucine Substituted Analogues of the Human Surfactant Protein SP-C
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-14T22%3A02%3A07IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Characterization%20of%20Poly-Leucine%20Substituted%20Analogues%20of%20the%20Human%20Surfactant%20Protein%20SP-C&rft.jtitle=Biological%20&%20pharmaceutical%20bulletin&rft.au=TAKEI,%20Tsunetomo&rft.date=1996-12-01&rft.volume=19&rft.issue=12&rft.spage=1550&rft.epage=1555&rft.pages=1550-1555&rft.issn=0918-6158&rft.eissn=1347-5215&rft_id=info:doi/10.1248/bpb.19.1550&rft_dat=%3Cproquest_cross%3E3120325061%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1449162940&rft_id=info:pmid/8996637&rfr_iscdi=true