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Understanding the Transepithelial Transport and Transbilayer Diffusion of the Antihypertensive Peptide Asn-Cys-Trp: Insights from Caco‑2 Cell Monolayers and the DPPC Model Membrane
Understanding the transport mechanism of the peptide Asn-Cys-Trp (NCW) is crucial to improving its intestinal absorption and bioavailability. This study investigated the absorption of NCW through Caco-2 cell monolayers and its interaction with the DPPC bilayers. Results revealed that after a 3 h inc...
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Published in: | Journal of agricultural and food chemistry 2024-05, Vol.72 (17), p.9828-9841 |
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creator | Wu, Sijia Jiang, Ping Zhang, Xiaoliang Mao, Chen Dai, Yaxi Zhuang, Hong Pang, Yong |
description | Understanding the transport mechanism of the peptide Asn-Cys-Trp (NCW) is crucial to improving its intestinal absorption and bioavailability. This study investigated the absorption of NCW through Caco-2 cell monolayers and its interaction with the DPPC bilayers. Results revealed that after a 3 h incubation, the Papp (AP-BL) and Papp (BL-AP) values of NCW at a concentration of 5 mmol/L were (22.24 ± 4.52) × 10–7 and (6.63 ± 2.31) × 10–7 cm/s, respectively, with the transport rates of 1.59 ± 0.32 and 0.62 ± 0.20%, indicating its moderate absorption. NCW was found to be transported via PepT1 and paracellular transport pathways, as evidenced by the significant impact of Gly-Pro and cytochalasin D on the Papp values. Moreover, NCW upregulated ZO-1 mRNA expression. Further investigation of the ZO-1-mediated interaction between NCW and tight junction proteins will contribute to a better understanding of the paracellular transport mechanism of NCW. The interaction between NCW and the DPPC bilayers was predominantly driven by entropy. NCW permeated the bilayers through electrostatic, hydrogen bonding, and hydrophobic interactions, resulting in increased fluidity, flexibility, and disorder as well as phase transition and phase separation of the bilayers. |
doi_str_mv | 10.1021/acs.jafc.4c00155 |
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This study investigated the absorption of NCW through Caco-2 cell monolayers and its interaction with the DPPC bilayers. Results revealed that after a 3 h incubation, the Papp (AP-BL) and Papp (BL-AP) values of NCW at a concentration of 5 mmol/L were (22.24 ± 4.52) × 10–7 and (6.63 ± 2.31) × 10–7 cm/s, respectively, with the transport rates of 1.59 ± 0.32 and 0.62 ± 0.20%, indicating its moderate absorption. NCW was found to be transported via PepT1 and paracellular transport pathways, as evidenced by the significant impact of Gly-Pro and cytochalasin D on the Papp values. Moreover, NCW upregulated ZO-1 mRNA expression. Further investigation of the ZO-1-mediated interaction between NCW and tight junction proteins will contribute to a better understanding of the paracellular transport mechanism of NCW. The interaction between NCW and the DPPC bilayers was predominantly driven by entropy. NCW permeated the bilayers through electrostatic, hydrogen bonding, and hydrophobic interactions, resulting in increased fluidity, flexibility, and disorder as well as phase transition and phase separation of the bilayers.</description><identifier>ISSN: 0021-8561</identifier><identifier>EISSN: 1520-5118</identifier><identifier>DOI: 10.1021/acs.jafc.4c00155</identifier><identifier>PMID: 38639269</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>1,2-Dipalmitoylphosphatidylcholine - chemistry ; 1,2-Dipalmitoylphosphatidylcholine - metabolism ; Antihypertensive Agents - chemistry ; Antihypertensive Agents - metabolism ; Bioactive Constituents, Metabolites, and Functions ; Biological Transport ; Caco-2 Cells ; Diffusion ; Humans ; Lipid Bilayers - chemistry ; Lipid Bilayers - metabolism ; Oligopeptides - chemistry ; Oligopeptides - metabolism ; Zonula Occludens-1 Protein - genetics ; Zonula Occludens-1 Protein - metabolism</subject><ispartof>Journal of agricultural and food chemistry, 2024-05, Vol.72 (17), p.9828-9841</ispartof><rights>2024 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a336t-2bea8bd64544ab89e8405bfde74869d8f66da5bd9ff894b6057730330c60b1b93</citedby><cites>FETCH-LOGICAL-a336t-2bea8bd64544ab89e8405bfde74869d8f66da5bd9ff894b6057730330c60b1b93</cites><orcidid>0000-0002-9767-9966</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38639269$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wu, Sijia</creatorcontrib><creatorcontrib>Jiang, Ping</creatorcontrib><creatorcontrib>Zhang, Xiaoliang</creatorcontrib><creatorcontrib>Mao, Chen</creatorcontrib><creatorcontrib>Dai, Yaxi</creatorcontrib><creatorcontrib>Zhuang, Hong</creatorcontrib><creatorcontrib>Pang, Yong</creatorcontrib><title>Understanding the Transepithelial Transport and Transbilayer Diffusion of the Antihypertensive Peptide Asn-Cys-Trp: Insights from Caco‑2 Cell Monolayers and the DPPC Model Membrane</title><title>Journal of agricultural and food chemistry</title><addtitle>J. Agric. Food Chem</addtitle><description>Understanding the transport mechanism of the peptide Asn-Cys-Trp (NCW) is crucial to improving its intestinal absorption and bioavailability. This study investigated the absorption of NCW through Caco-2 cell monolayers and its interaction with the DPPC bilayers. Results revealed that after a 3 h incubation, the Papp (AP-BL) and Papp (BL-AP) values of NCW at a concentration of 5 mmol/L were (22.24 ± 4.52) × 10–7 and (6.63 ± 2.31) × 10–7 cm/s, respectively, with the transport rates of 1.59 ± 0.32 and 0.62 ± 0.20%, indicating its moderate absorption. NCW was found to be transported via PepT1 and paracellular transport pathways, as evidenced by the significant impact of Gly-Pro and cytochalasin D on the Papp values. Moreover, NCW upregulated ZO-1 mRNA expression. Further investigation of the ZO-1-mediated interaction between NCW and tight junction proteins will contribute to a better understanding of the paracellular transport mechanism of NCW. The interaction between NCW and the DPPC bilayers was predominantly driven by entropy. NCW permeated the bilayers through electrostatic, hydrogen bonding, and hydrophobic interactions, resulting in increased fluidity, flexibility, and disorder as well as phase transition and phase separation of the bilayers.</description><subject>1,2-Dipalmitoylphosphatidylcholine - chemistry</subject><subject>1,2-Dipalmitoylphosphatidylcholine - metabolism</subject><subject>Antihypertensive Agents - chemistry</subject><subject>Antihypertensive Agents - metabolism</subject><subject>Bioactive Constituents, Metabolites, and Functions</subject><subject>Biological Transport</subject><subject>Caco-2 Cells</subject><subject>Diffusion</subject><subject>Humans</subject><subject>Lipid Bilayers - chemistry</subject><subject>Lipid Bilayers - metabolism</subject><subject>Oligopeptides - chemistry</subject><subject>Oligopeptides - metabolism</subject><subject>Zonula Occludens-1 Protein - genetics</subject><subject>Zonula Occludens-1 Protein - metabolism</subject><issn>0021-8561</issn><issn>1520-5118</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp1UbuO1DAUtRCIHRZ6KuSSggx2HDsO3SrLY6VFTDFbR3Z8veNVxg52stJ0_AI_wwfxJXgmAx2VfX0e91gHodeUrCkp6XvVp_WDsv266gmhnD9BK8pLUnBK5VO0IplTSC7oBXqR0gMhRPKaPEcXTArWlKJZoV933kBMk_LG-Xs87QBvo_IJRpfvg1PDMo8hTjiTlkm7QR0g4mtn7Zxc8DjYk_bKT253GCFO4JN7BLyBcXImA8kX7SEV2zh-wDcZu99NCdsY9rhVffj942eJWxgG_DX4cDJPp3VH0-vNps3vBjIKe50DwEv0zKohwavzeYnuPn3ctl-K22-fb9qr20IxJqai1KCkNqLiVaW0bEBWhGtroK6kaIy0QhjFtWmslU2lBeF1zQhjpBdEU92wS_R28R1j-D5Dmrq9S33OmTOEOXWMVIzUrKp5ppKF2seQUgTbjdHtVTx0lHTHtrrcVndsqzu3lSVvzu6z3oP5J_hbTya8WwgnaZijz5_9v98fBPKkuw</recordid><startdate>20240501</startdate><enddate>20240501</enddate><creator>Wu, Sijia</creator><creator>Jiang, Ping</creator><creator>Zhang, Xiaoliang</creator><creator>Mao, Chen</creator><creator>Dai, Yaxi</creator><creator>Zhuang, Hong</creator><creator>Pang, Yong</creator><general>American Chemical Society</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><orcidid>https://orcid.org/0000-0002-9767-9966</orcidid></search><sort><creationdate>20240501</creationdate><title>Understanding the Transepithelial Transport and Transbilayer Diffusion of the Antihypertensive Peptide Asn-Cys-Trp: Insights from Caco‑2 Cell Monolayers and the DPPC Model Membrane</title><author>Wu, Sijia ; Jiang, Ping ; Zhang, Xiaoliang ; Mao, Chen ; Dai, Yaxi ; Zhuang, Hong ; Pang, Yong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a336t-2bea8bd64544ab89e8405bfde74869d8f66da5bd9ff894b6057730330c60b1b93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>1,2-Dipalmitoylphosphatidylcholine - chemistry</topic><topic>1,2-Dipalmitoylphosphatidylcholine - metabolism</topic><topic>Antihypertensive Agents - chemistry</topic><topic>Antihypertensive Agents - metabolism</topic><topic>Bioactive Constituents, Metabolites, and Functions</topic><topic>Biological Transport</topic><topic>Caco-2 Cells</topic><topic>Diffusion</topic><topic>Humans</topic><topic>Lipid Bilayers - chemistry</topic><topic>Lipid Bilayers - metabolism</topic><topic>Oligopeptides - chemistry</topic><topic>Oligopeptides - metabolism</topic><topic>Zonula Occludens-1 Protein - genetics</topic><topic>Zonula Occludens-1 Protein - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wu, Sijia</creatorcontrib><creatorcontrib>Jiang, Ping</creatorcontrib><creatorcontrib>Zhang, Xiaoliang</creatorcontrib><creatorcontrib>Mao, Chen</creatorcontrib><creatorcontrib>Dai, Yaxi</creatorcontrib><creatorcontrib>Zhuang, Hong</creatorcontrib><creatorcontrib>Pang, Yong</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>Journal of agricultural and food chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wu, Sijia</au><au>Jiang, Ping</au><au>Zhang, Xiaoliang</au><au>Mao, Chen</au><au>Dai, Yaxi</au><au>Zhuang, Hong</au><au>Pang, Yong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Understanding the Transepithelial Transport and Transbilayer Diffusion of the Antihypertensive Peptide Asn-Cys-Trp: Insights from Caco‑2 Cell Monolayers and the DPPC Model Membrane</atitle><jtitle>Journal of agricultural and food chemistry</jtitle><addtitle>J. Agric. Food Chem</addtitle><date>2024-05-01</date><risdate>2024</risdate><volume>72</volume><issue>17</issue><spage>9828</spage><epage>9841</epage><pages>9828-9841</pages><issn>0021-8561</issn><eissn>1520-5118</eissn><abstract>Understanding the transport mechanism of the peptide Asn-Cys-Trp (NCW) is crucial to improving its intestinal absorption and bioavailability. This study investigated the absorption of NCW through Caco-2 cell monolayers and its interaction with the DPPC bilayers. Results revealed that after a 3 h incubation, the Papp (AP-BL) and Papp (BL-AP) values of NCW at a concentration of 5 mmol/L were (22.24 ± 4.52) × 10–7 and (6.63 ± 2.31) × 10–7 cm/s, respectively, with the transport rates of 1.59 ± 0.32 and 0.62 ± 0.20%, indicating its moderate absorption. NCW was found to be transported via PepT1 and paracellular transport pathways, as evidenced by the significant impact of Gly-Pro and cytochalasin D on the Papp values. Moreover, NCW upregulated ZO-1 mRNA expression. Further investigation of the ZO-1-mediated interaction between NCW and tight junction proteins will contribute to a better understanding of the paracellular transport mechanism of NCW. The interaction between NCW and the DPPC bilayers was predominantly driven by entropy. NCW permeated the bilayers through electrostatic, hydrogen bonding, and hydrophobic interactions, resulting in increased fluidity, flexibility, and disorder as well as phase transition and phase separation of the bilayers.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>38639269</pmid><doi>10.1021/acs.jafc.4c00155</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0002-9767-9966</orcidid></addata></record> |
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subjects | 1,2-Dipalmitoylphosphatidylcholine - chemistry 1,2-Dipalmitoylphosphatidylcholine - metabolism Antihypertensive Agents - chemistry Antihypertensive Agents - metabolism Bioactive Constituents, Metabolites, and Functions Biological Transport Caco-2 Cells Diffusion Humans Lipid Bilayers - chemistry Lipid Bilayers - metabolism Oligopeptides - chemistry Oligopeptides - metabolism Zonula Occludens-1 Protein - genetics Zonula Occludens-1 Protein - metabolism |
title | Understanding the Transepithelial Transport and Transbilayer Diffusion of the Antihypertensive Peptide Asn-Cys-Trp: Insights from Caco‑2 Cell Monolayers and the DPPC Model Membrane |
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