抗纤颤肽 TNGQ 与胰岛淀粉样多肽的跨域结合可在巨型单层囊泡和胰腺 β 细胞中发挥细胞保护作用。

IF 5.1 1区 农林科学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Food & Function Pub Date : 2024-11-20 DOI:10.1039/d4fo03322a
Raliat O Abioye, Martha S Yiridoe, Chenyang Wang, Tyler J Avis, Tamer A E Ahmed, Riadh Hammami, Chibuike C Udenigwe
{"title":"抗纤颤肽 TNGQ 与胰岛淀粉样多肽的跨域结合可在巨型单层囊泡和胰腺 β 细胞中发挥细胞保护作用。","authors":"Raliat O Abioye, Martha S Yiridoe, Chenyang Wang, Tyler J Avis, Tamer A E Ahmed, Riadh Hammami, Chibuike C Udenigwe","doi":"10.1039/d4fo03322a","DOIUrl":null,"url":null,"abstract":"<p><p>Islet amyloid polypeptide (IAPP) fibrillation induces β-cell dysfunction and toxicity in patients with type 2 diabetes. Cytotoxicity is caused by the ability of IAPP fibrils and fibrillar intermediates to permeate the cellular membrane of pancreatic β-cells, trigger endoplasmic reticular stress, induce reactive oxygen species production, and upregulate apoptosis-related genes. Thus, inhibition of IAPP fibrillation is of great interest for preventing associated cytotoxicity. In this study, the cellular protective effects of three anti-fibrillation tetrapeptides, YMSV, MANT, and TNGQ, against IAPP fibrillation-induced membrane leakage in giant unilamellar vesicles (GUVs) and toxicity in RIN-m cells were evaluated. The anti-fibrillation activity of TNGQ translated to cytoprotective effects as it resulted in a 69.0 ± 7.9% decrease in calcein release in GUVs and a significant increase in cell viability from 6.4 ± 6.4% with IAPP to 47.5 ± 3.8% with the addition of TNGQ. MANT slightly inhibited IAPP-induced GUV leakage and increased cell viability. In contrast, the protective effect of YMSV against IAPP fibrillation-induced membrane damage in GUVs was completely diminished in β-cells. Molecular docking of pentameric IAPP showed that Asn21 and Asn22 of IAPP are important for inhibitor binding, which, coupled with the cross-domain binding interactions of TNGQ, explains its stronger anti-fibrillation and cytoprotective effects than MANT and YMSV. These findings provide insights into the functional significance of peptide-IAPP binding interactions in mitigating fibrillation and IAPP fibrillation-induced cytotoxicity.</p>","PeriodicalId":77,"journal":{"name":"Food & Function","volume":" ","pages":""},"PeriodicalIF":5.1000,"publicationDate":"2024-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Cross-domain binding of anti-fibrillation peptide TNGQ to islet amyloid polypeptide provides cytoprotective effects in giant unilamellar vesicles and pancreatic β-cells.\",\"authors\":\"Raliat O Abioye, Martha S Yiridoe, Chenyang Wang, Tyler J Avis, Tamer A E Ahmed, Riadh Hammami, Chibuike C Udenigwe\",\"doi\":\"10.1039/d4fo03322a\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Islet amyloid polypeptide (IAPP) fibrillation induces β-cell dysfunction and toxicity in patients with type 2 diabetes. Cytotoxicity is caused by the ability of IAPP fibrils and fibrillar intermediates to permeate the cellular membrane of pancreatic β-cells, trigger endoplasmic reticular stress, induce reactive oxygen species production, and upregulate apoptosis-related genes. Thus, inhibition of IAPP fibrillation is of great interest for preventing associated cytotoxicity. In this study, the cellular protective effects of three anti-fibrillation tetrapeptides, YMSV, MANT, and TNGQ, against IAPP fibrillation-induced membrane leakage in giant unilamellar vesicles (GUVs) and toxicity in RIN-m cells were evaluated. The anti-fibrillation activity of TNGQ translated to cytoprotective effects as it resulted in a 69.0 ± 7.9% decrease in calcein release in GUVs and a significant increase in cell viability from 6.4 ± 6.4% with IAPP to 47.5 ± 3.8% with the addition of TNGQ. MANT slightly inhibited IAPP-induced GUV leakage and increased cell viability. In contrast, the protective effect of YMSV against IAPP fibrillation-induced membrane damage in GUVs was completely diminished in β-cells. Molecular docking of pentameric IAPP showed that Asn21 and Asn22 of IAPP are important for inhibitor binding, which, coupled with the cross-domain binding interactions of TNGQ, explains its stronger anti-fibrillation and cytoprotective effects than MANT and YMSV. These findings provide insights into the functional significance of peptide-IAPP binding interactions in mitigating fibrillation and IAPP fibrillation-induced cytotoxicity.</p>\",\"PeriodicalId\":77,\"journal\":{\"name\":\"Food & Function\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":5.1000,\"publicationDate\":\"2024-11-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Food & Function\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://doi.org/10.1039/d4fo03322a\",\"RegionNum\":1,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Food & Function","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1039/d4fo03322a","RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

胰岛淀粉样多肽(IAPP)纤维化会诱发2型糖尿病患者的β细胞功能障碍和毒性。细胞毒性是由 IAPP 纤维和纤维状中间产物渗透胰腺 β 细胞的细胞膜、引发内质网应激、诱导活性氧生成和上调凋亡相关基因的能力造成的。因此,抑制 IAPP 纤维化对于防止相关的细胞毒性具有重要意义。本研究评估了三种抗纤化四肽(YMSV、MANT和TNGQ)对IAPP纤化诱导的巨型单纤毛泡(GUVs)膜渗漏和RIN-m细胞毒性的细胞保护作用。TNGQ 的抗纤化活性转化为细胞保护作用,因为它使 GUVs 中的钙蓝蛋白释放量减少了 69.0 ± 7.9%,并使细胞存活率从 IAPP 诱导的 6.4 ± 6.4% 显著提高到 TNGQ 诱导的 47.5 ± 3.8%。MANT 可轻微抑制 IAPP 诱导的 GUV 泄漏并提高细胞活力。相反,YMSV 对 IAPP 纤维化诱导的 GUV 膜损伤的保护作用在 β 细胞中完全减弱。五聚体 IAPP 的分子对接显示,IAPP 的 Asn21 和 Asn22 对抑制剂的结合很重要,再加上 TNGQ 的跨域结合相互作用,这就解释了为什么 TNGQ 比 MANT 和 YMSV 具有更强的抗纤化和细胞保护作用。这些发现让我们深入了解了多肽-IAPP结合相互作用在减轻纤颤和IAPP纤颤诱导的细胞毒性方面的功能意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cross-domain binding of anti-fibrillation peptide TNGQ to islet amyloid polypeptide provides cytoprotective effects in giant unilamellar vesicles and pancreatic β-cells.

Islet amyloid polypeptide (IAPP) fibrillation induces β-cell dysfunction and toxicity in patients with type 2 diabetes. Cytotoxicity is caused by the ability of IAPP fibrils and fibrillar intermediates to permeate the cellular membrane of pancreatic β-cells, trigger endoplasmic reticular stress, induce reactive oxygen species production, and upregulate apoptosis-related genes. Thus, inhibition of IAPP fibrillation is of great interest for preventing associated cytotoxicity. In this study, the cellular protective effects of three anti-fibrillation tetrapeptides, YMSV, MANT, and TNGQ, against IAPP fibrillation-induced membrane leakage in giant unilamellar vesicles (GUVs) and toxicity in RIN-m cells were evaluated. The anti-fibrillation activity of TNGQ translated to cytoprotective effects as it resulted in a 69.0 ± 7.9% decrease in calcein release in GUVs and a significant increase in cell viability from 6.4 ± 6.4% with IAPP to 47.5 ± 3.8% with the addition of TNGQ. MANT slightly inhibited IAPP-induced GUV leakage and increased cell viability. In contrast, the protective effect of YMSV against IAPP fibrillation-induced membrane damage in GUVs was completely diminished in β-cells. Molecular docking of pentameric IAPP showed that Asn21 and Asn22 of IAPP are important for inhibitor binding, which, coupled with the cross-domain binding interactions of TNGQ, explains its stronger anti-fibrillation and cytoprotective effects than MANT and YMSV. These findings provide insights into the functional significance of peptide-IAPP binding interactions in mitigating fibrillation and IAPP fibrillation-induced cytotoxicity.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Food & Function
Food & Function BIOCHEMISTRY & MOLECULAR BIOLOGY-FOOD SCIENCE & TECHNOLOGY
CiteScore
10.10
自引率
6.60%
发文量
957
审稿时长
1.8 months
期刊介绍: Food & Function provides a unique venue for physicists, chemists, biochemists, nutritionists and other food scientists to publish work at the interface of the chemistry, physics and biology of food. The journal focuses on food and the functions of food in relation to health.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信