Mehmet B. Karakaplan, Vinay S. Tiwari, Omer Agazani, Cécile Echalier, Gilles Subra and Meital Reches
{"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}
引用次数: 0
Abstract
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.