Amphipathic peptide–phospholipid nanofibers: Kinetics of fiber formation and molecular transfer between assemblies
Understanding the kinetics of nano-assembly formation is important to elucidate the biological processes involved and develop novel nanomaterials with biological functions. In the present study, we report the kinetic mechanisms of nanofiber formation from a mixture of phospholipids and the amphipath...
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Veröffentlicht in: | Biophysical chemistry 2023-05, Vol.296, p.106985-106985, Article 106985 |
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description | Understanding the kinetics of nano-assembly formation is important to elucidate the biological processes involved and develop novel nanomaterials with biological functions. In the present study, we report the kinetic mechanisms of nanofiber formation from a mixture of phospholipids and the amphipathic peptide 18A[A11C], carrying cysteine substitution of the apolipoprotein A-I-derived peptide 18A at residue 11. 18A[A11C] with acetylated N-terminus and amidated C-terminus can associate with phosphatidylcholine to form fibrous aggregates at neutral pH and lipid-to-peptide molar ratio of ∼1, although the reaction pathways of self-assembly remain unclear. Here, the peptide was added to giant 1-palmitoyl-2-oleoyl phosphatidylcholine vesicles to monitor nanofiber formation under fluorescence microscopy. The peptide initially solubilized the lipid vesicles into particles smaller than the resolution of optical microscope, and fibrous aggregates appeared subsequently. Transmission electron microscopy and dynamic light scattering analyses revealed that the vesicle-solubilized particles were spherical or circular, measuring ∼10–20 nm in diameter. The rate of nanofiber formation of 18A with 1,2-dipalmitoyl phosphatidylcholine from the particles was proportional to the square of lipid–peptide concentration in the system, suggesting that the association of particles, accompanied by conformational changes, was the rate-limiting step. Moreover, molecules in the nanofibers could be transferred between aggregates faster than those in the lipid vesicles. These findings provide useful information for the development and control of nano-assembling structures using peptides and phospholipids.
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•Chemical kinetics of phospholipid–peptide nanofiber formation is investigated.•18A[A11C] peptide first solubilizes lipid vesicles into small micellar particles.•Nanofibers are formed by the association of the small particles.•The lipid transfer between nanofibers is more facilitated than between vesicles. |
doi_str_mv | 10.1016/j.bpc.2023.106985 |
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[Display omitted]
•Chemical kinetics of phospholipid–peptide nanofiber formation is investigated.•18A[A11C] peptide first solubilizes lipid vesicles into small micellar particles.•Nanofibers are formed by the association of the small particles.•The lipid transfer between nanofibers is more facilitated than between vesicles.</description><identifier>ISSN: 0301-4622</identifier><identifier>EISSN: 1873-4200</identifier><identifier>DOI: 10.1016/j.bpc.2023.106985</identifier><identifier>PMID: 36863073</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Amino Acid Sequence ; Kinetics ; Lipid transfer ; Nanofiber ; Nanofibers ; Peptide ; Peptides - chemistry ; Phosphatidylcholines ; Phospholipid ; Phospholipids - metabolism ; Reaction kinetics ; Self-assembly</subject><ispartof>Biophysical chemistry, 2023-05, Vol.296, p.106985-106985, Article 106985</ispartof><rights>2023 Elsevier B.V.</rights><rights>Copyright © 2023 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c419t-f2335808e5633e4be7f18dd404dde1732f538ff74c1966f0d3a25aafdd5cfe5f3</citedby><cites>FETCH-LOGICAL-c419t-f2335808e5633e4be7f18dd404dde1732f538ff74c1966f0d3a25aafdd5cfe5f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0301462223000364$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36863073$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shimizu, Chinatsu</creatorcontrib><creatorcontrib>Ikeda, Keisuke</creatorcontrib><creatorcontrib>Nakao, Hiroyuki</creatorcontrib><creatorcontrib>Nakano, Minoru</creatorcontrib><title>Amphipathic peptide–phospholipid nanofibers: Kinetics of fiber formation and molecular transfer between assemblies</title><title>Biophysical chemistry</title><addtitle>Biophys Chem</addtitle><description>Understanding the kinetics of nano-assembly formation is important to elucidate the biological processes involved and develop novel nanomaterials with biological functions. In the present study, we report the kinetic mechanisms of nanofiber formation from a mixture of phospholipids and the amphipathic peptide 18A[A11C], carrying cysteine substitution of the apolipoprotein A-I-derived peptide 18A at residue 11. 18A[A11C] with acetylated N-terminus and amidated C-terminus can associate with phosphatidylcholine to form fibrous aggregates at neutral pH and lipid-to-peptide molar ratio of ∼1, although the reaction pathways of self-assembly remain unclear. Here, the peptide was added to giant 1-palmitoyl-2-oleoyl phosphatidylcholine vesicles to monitor nanofiber formation under fluorescence microscopy. The peptide initially solubilized the lipid vesicles into particles smaller than the resolution of optical microscope, and fibrous aggregates appeared subsequently. Transmission electron microscopy and dynamic light scattering analyses revealed that the vesicle-solubilized particles were spherical or circular, measuring ∼10–20 nm in diameter. The rate of nanofiber formation of 18A with 1,2-dipalmitoyl phosphatidylcholine from the particles was proportional to the square of lipid–peptide concentration in the system, suggesting that the association of particles, accompanied by conformational changes, was the rate-limiting step. Moreover, molecules in the nanofibers could be transferred between aggregates faster than those in the lipid vesicles. These findings provide useful information for the development and control of nano-assembling structures using peptides and phospholipids.
[Display omitted]
•Chemical kinetics of phospholipid–peptide nanofiber formation is investigated.•18A[A11C] peptide first solubilizes lipid vesicles into small micellar particles.•Nanofibers are formed by the association of the small particles.•The lipid transfer between nanofibers is more facilitated than between vesicles.</description><subject>Amino Acid Sequence</subject><subject>Kinetics</subject><subject>Lipid transfer</subject><subject>Nanofiber</subject><subject>Nanofibers</subject><subject>Peptide</subject><subject>Peptides - chemistry</subject><subject>Phosphatidylcholines</subject><subject>Phospholipid</subject><subject>Phospholipids - metabolism</subject><subject>Reaction kinetics</subject><subject>Self-assembly</subject><issn>0301-4622</issn><issn>1873-4200</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kM1OGzEQx62qqAmBB-il8rGXDf7YD4eeUNQCIhIXOFtee6w42l27tlPUW9-hb8iT4DTQIyONRjPzn780P4Q-U7KkhLYXu2Uf9JIRxkvfrkTzAc2p6HhVM0I-ojnhhFZ1y9gMnaa0IyUEIZ_QjLei5aTjc5SvxrB1QeWt0zhAyM7A85-_YetTycEFZ_CkJm9dDzFd4js3QXY6YW_xvxm2Po4qOz9hNRk8-gH0flAR56imZIugh_wEUNYpwdgPDtIZOrFqSHD-Whfo8cf3h_VNtbm_vl1fbSpd01WuLOO8EURA03IOdQ-dpcKYmtTGAO04sw0X1na1pqu2tcRwxRqlrDGNttBYvkBfj74h-p97SFmOLmkYBjWB3yfJOsHrFRcF4ALRo1RHn1IEK0N0o4q_JSXyAFvuZIEtD7DlEXa5-fJqv-9HMP8v3ugWwbejAMqTvxxEmbSDSYNxEXSWxrt37F8At9iTQw</recordid><startdate>202305</startdate><enddate>202305</enddate><creator>Shimizu, Chinatsu</creator><creator>Ikeda, Keisuke</creator><creator>Nakao, Hiroyuki</creator><creator>Nakano, Minoru</creator><general>Elsevier B.V</general><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></search><sort><creationdate>202305</creationdate><title>Amphipathic peptide–phospholipid nanofibers: Kinetics of fiber formation and molecular transfer between assemblies</title><author>Shimizu, Chinatsu ; Ikeda, Keisuke ; Nakao, Hiroyuki ; Nakano, Minoru</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c419t-f2335808e5633e4be7f18dd404dde1732f538ff74c1966f0d3a25aafdd5cfe5f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Amino Acid Sequence</topic><topic>Kinetics</topic><topic>Lipid transfer</topic><topic>Nanofiber</topic><topic>Nanofibers</topic><topic>Peptide</topic><topic>Peptides - chemistry</topic><topic>Phosphatidylcholines</topic><topic>Phospholipid</topic><topic>Phospholipids - metabolism</topic><topic>Reaction kinetics</topic><topic>Self-assembly</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shimizu, Chinatsu</creatorcontrib><creatorcontrib>Ikeda, Keisuke</creatorcontrib><creatorcontrib>Nakao, Hiroyuki</creatorcontrib><creatorcontrib>Nakano, Minoru</creatorcontrib><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><jtitle>Biophysical chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shimizu, Chinatsu</au><au>Ikeda, Keisuke</au><au>Nakao, Hiroyuki</au><au>Nakano, Minoru</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Amphipathic peptide–phospholipid nanofibers: Kinetics of fiber formation and molecular transfer between assemblies</atitle><jtitle>Biophysical chemistry</jtitle><addtitle>Biophys Chem</addtitle><date>2023-05</date><risdate>2023</risdate><volume>296</volume><spage>106985</spage><epage>106985</epage><pages>106985-106985</pages><artnum>106985</artnum><issn>0301-4622</issn><eissn>1873-4200</eissn><abstract>Understanding the kinetics of nano-assembly formation is important to elucidate the biological processes involved and develop novel nanomaterials with biological functions. In the present study, we report the kinetic mechanisms of nanofiber formation from a mixture of phospholipids and the amphipathic peptide 18A[A11C], carrying cysteine substitution of the apolipoprotein A-I-derived peptide 18A at residue 11. 18A[A11C] with acetylated N-terminus and amidated C-terminus can associate with phosphatidylcholine to form fibrous aggregates at neutral pH and lipid-to-peptide molar ratio of ∼1, although the reaction pathways of self-assembly remain unclear. Here, the peptide was added to giant 1-palmitoyl-2-oleoyl phosphatidylcholine vesicles to monitor nanofiber formation under fluorescence microscopy. The peptide initially solubilized the lipid vesicles into particles smaller than the resolution of optical microscope, and fibrous aggregates appeared subsequently. Transmission electron microscopy and dynamic light scattering analyses revealed that the vesicle-solubilized particles were spherical or circular, measuring ∼10–20 nm in diameter. The rate of nanofiber formation of 18A with 1,2-dipalmitoyl phosphatidylcholine from the particles was proportional to the square of lipid–peptide concentration in the system, suggesting that the association of particles, accompanied by conformational changes, was the rate-limiting step. Moreover, molecules in the nanofibers could be transferred between aggregates faster than those in the lipid vesicles. These findings provide useful information for the development and control of nano-assembling structures using peptides and phospholipids.
[Display omitted]
•Chemical kinetics of phospholipid–peptide nanofiber formation is investigated.•18A[A11C] peptide first solubilizes lipid vesicles into small micellar particles.•Nanofibers are formed by the association of the small particles.•The lipid transfer between nanofibers is more facilitated than between vesicles.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>36863073</pmid><doi>10.1016/j.bpc.2023.106985</doi><tpages>1</tpages></addata></record> |
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subjects | Amino Acid Sequence Kinetics Lipid transfer Nanofiber Nanofibers Peptide Peptides - chemistry Phosphatidylcholines Phospholipid Phospholipids - metabolism Reaction kinetics Self-assembly |
title | Amphipathic peptide–phospholipid nanofibers: Kinetics of fiber formation and molecular transfer between assemblies |
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