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一种在生物材料上定量合成肽浓度的简易方法。

A Facile Method to Quantify Synthetic Peptide Concentrations on Biomaterials.

机构信息

Department of Materials, Department of Bioengineering and Institute of Biomedical Engineering, Imperial College London, London, SW7 2AZ, United Kingdom.

Kavli Institute for Nanoscience Discovery, Department of Physiology, Anatomy and Genetics, Department of Engineering Science, University of Oxford, Oxford, OX1 3QU, United Kingdom.

出版信息

ACS Appl Mater Interfaces. 2024 Sep 18;16(37):49880-49888. doi: 10.1021/acsami.4c07164. Epub 2024 Sep 9.

Abstract

While it is well understood that peptides can greatly improve cell-material interactions, it is often challenging to determine the concentration of the peptide which decorates a material. Herein, we describe a straightforward method using readily, synthetically accessible Fmoc peptides and commercially available reagents to measure the concentration of peptides on nanoparticles, surfaces, and hydrogels. To achieve this, the Fmoc protecting group from immobilized peptides is removed under optimized basic conditions. The dibenzofulvene released can be quantified by HPLC or UV-vis spectroscopy, enabling a direct experimental measurement of the concentration of the peptide. We show that we can measure the concentration of a BMP-2 peptide mimic on a hydrogel to determine the concentration required to stimulate osteogenesis of human mesenchymal stem cells. We envision that this methodology will enable a more thorough understanding of the concentration of synthetic peptides decorated on many biomaterials (e.g., nanoparticles, surfaces, hydrogels) to improve deconvolution of the interactions at the cell-material interface.

摘要

虽然人们已经充分了解到肽可以极大地改善细胞与材料的相互作用,但确定修饰材料的肽的浓度通常具有挑战性。在此,我们描述了一种使用现成的、易于合成的 Fmoc 肽和市售试剂来测量纳米颗粒、表面和水凝胶上肽浓度的简单方法。为了实现这一点,在优化的碱性条件下去除固定化肽的 Fmoc 保护基团。通过 HPLC 或 UV-vis 光谱法可以定量测定释放的二苯并富烯,从而可以直接测量肽的浓度。我们表明,我们可以测量水凝胶上 BMP-2 肽模拟物的浓度,以确定刺激人骨髓间充质干细胞成骨所需的浓度。我们设想这种方法将使我们能够更深入地了解许多生物材料(例如纳米颗粒、表面、水凝胶)上修饰的合成肽的浓度,从而改善细胞-材料界面相互作用的解卷积。

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