Mehmet B. Karakaplan, Vinay S. Tiwari, Omer Agazani, Cécile Echalier, Gilles Subra and Meital Reches
{"title":"硅基化多肽作为溶胶-凝胶聚合材料合成的基石。","authors":"Mehmet B. Karakaplan, Vinay S. Tiwari, Omer Agazani, Cécile Echalier, Gilles Subra and Meital Reches","doi":"10.1039/D5FD00014A","DOIUrl":null,"url":null,"abstract":"<p >The bottom-up approach exploits simple building blocks to generate new materials with desired physical and chemical characteristics. Here, we combine two bottom-up routes that occur under mild conditions, self-assembly and sol–gel synthesis, to program the shape and structure of materials. While self-assembly occurs through non-covalent interactions, sol–gel synthesis involves forming covalent bonds. As a proof of concept, we chose the self-assembled peptide Phe-Phe and its fluorinated analogue Phe(4-F)-Phe(4-F) to template the sol–gel process. These peptides were silylated to allow their self-mineralization. Scanning electron microscopy and atomic force microscope analysis revealed the formation of rod-shaped structures for the silylated Phe-Phe while spherical particles were formed by its fluorinated analogue. The size of the particles ranges from nano to micron scale. Fourier transform infrared spectrometry suggested the presence of parallel β-sheet secondary structure and siloxane bond formation that can stabilize these structures. Overall this approach can be adopted for other self-assembled peptides for generating new materials using a bottom-up approach.</p>","PeriodicalId":49075,"journal":{"name":"Faraday Discussions","volume":"260 ","pages":" 204-214"},"PeriodicalIF":3.1000,"publicationDate":"2025-02-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2025/fd/d5fd00014a?page=search","citationCount":"0","resultStr":"{\"title\":\"Silylated peptides as building blocks for material synthesis using sol–gel polymerization†\",\"authors\":\"Mehmet B. Karakaplan, Vinay S. Tiwari, Omer Agazani, Cécile Echalier, Gilles Subra and Meital Reches\",\"doi\":\"10.1039/D5FD00014A\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >The bottom-up approach exploits simple building blocks to generate new materials with desired physical and chemical characteristics. Here, we combine two bottom-up routes that occur under mild conditions, self-assembly and sol–gel synthesis, to program the shape and structure of materials. While self-assembly occurs through non-covalent interactions, sol–gel synthesis involves forming covalent bonds. As a proof of concept, we chose the self-assembled peptide Phe-Phe and its fluorinated analogue Phe(4-F)-Phe(4-F) to template the sol–gel process. These peptides were silylated to allow their self-mineralization. Scanning electron microscopy and atomic force microscope analysis revealed the formation of rod-shaped structures for the silylated Phe-Phe while spherical particles were formed by its fluorinated analogue. The size of the particles ranges from nano to micron scale. Fourier transform infrared spectrometry suggested the presence of parallel β-sheet secondary structure and siloxane bond formation that can stabilize these structures. Overall this approach can be adopted for other self-assembled peptides for generating new materials using a bottom-up approach.</p>\",\"PeriodicalId\":49075,\"journal\":{\"name\":\"Faraday Discussions\",\"volume\":\"260 \",\"pages\":\" 204-214\"},\"PeriodicalIF\":3.1000,\"publicationDate\":\"2025-02-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://pubs.rsc.org/en/content/articlepdf/2025/fd/d5fd00014a?page=search\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Faraday Discussions\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2025/fd/d5fd00014a\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"Chemistry\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Faraday Discussions","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/fd/d5fd00014a","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Chemistry","Score":null,"Total":0}
Silylated peptides as building blocks for material synthesis using sol–gel polymerization†
The bottom-up approach exploits simple building blocks to generate new materials with desired physical and chemical characteristics. Here, we combine two bottom-up routes that occur under mild conditions, self-assembly and sol–gel synthesis, to program the shape and structure of materials. While self-assembly occurs through non-covalent interactions, sol–gel synthesis involves forming covalent bonds. As a proof of concept, we chose the self-assembled peptide Phe-Phe and its fluorinated analogue Phe(4-F)-Phe(4-F) to template the sol–gel process. These peptides were silylated to allow their self-mineralization. Scanning electron microscopy and atomic force microscope analysis revealed the formation of rod-shaped structures for the silylated Phe-Phe while spherical particles were formed by its fluorinated analogue. The size of the particles ranges from nano to micron scale. Fourier transform infrared spectrometry suggested the presence of parallel β-sheet secondary structure and siloxane bond formation that can stabilize these structures. Overall this approach can be adopted for other self-assembled peptides for generating new materials using a bottom-up approach.