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噬菌体展示技术鉴定出指导碳酸钙多晶型形成的亲和素蛋白。

Phage display identifies Affimer proteins that direct calcium carbonate polymorph formation.

机构信息

School of Chemistry, University of Leeds, Leeds, LS2 9JT, UK.

School of Molecular and Cellular Biology and Astbury Centre for Structural Molecular Biology, University of Leeds, Leeds, LS2 9JT, UK.

出版信息

Biomater Sci. 2024 Oct 8;12(20):5215-5224. doi: 10.1039/d4bm00165f.

DOI:10.1039/d4bm00165f
PMID:39206560
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11358866/
Abstract

A key factor in biomineralization is the use of organic molecules to direct the formation of inorganic materials. However, identification of molecules that can selectively produce the calcium carbonate polymorphs calcite or aragonite has proven extremely challenging. Here, we use a phage display approach to identify proteins - rather than the short peptides typically identified using this method - that can direct calcium carbonate formation. A 1.3 × 10 library of Affimer proteins was displayed on modified M13 phage, where an Affimer is a ≈13 kDa protein scaffold that displays two variable regions of 9-13 residues. The phage displaying the Affimer library were then screened in binding assays against calcite and aragonite at pH 7.4, and four different strongly-binding proteins were identified. The two aragonite-binding proteins generated aragonite when calcium and magnesium ions were present at a 1 : 1 ratio, while the calcite-binding proteins produce magnesium-calcite under the same conditions. Calcite alone formed in the presence of all four proteins in the absence of magnesium ions. In combination with molecular dynamics simulations to evaluate the conformations of the proteins in solution, this work demonstrates the importance of conformation in polymorph control, and highlights the importance of magnesium ions, which are abundant in seawater, to reduce the energetic barriers associated with aragonite formation.

摘要

生物矿化的一个关键因素是利用有机分子来指导无机材料的形成。然而,鉴定能够选择性地产生方解石或文石两种碳酸钙多晶型的分子极具挑战性。在这里,我们使用噬菌体展示技术来鉴定能够指导碳酸钙形成的蛋白质,而不是通常使用该方法鉴定的短肽。我们展示了一个约 1.3×10 的 Affimer 蛋白库,Affimer 是一种约 13 kDa 的蛋白质支架,展示了两个 9-13 个残基的可变区。然后,在 pH 7.4 下,用结合测定法筛选与方解石和文石结合的噬菌体,鉴定出了 4 种不同的强结合蛋白。两种文石结合蛋白在钙离子和镁离子比例为 1:1 时生成文石,而方解石结合蛋白在相同条件下生成镁方解石。在没有镁离子的情况下,这四种蛋白都能单独形成方解石。结合分子动力学模拟来评估蛋白质在溶液中的构象,这项工作证明了构象在多晶型控制中的重要性,并强调了海水中丰富的镁离子的重要性,因为镁离子可以降低文石形成的能量障碍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0bb2/11358866/414e86af69c3/d4bm00165f-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0bb2/11358866/4f5f33f0e595/d4bm00165f-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0bb2/11358866/2d14f8686fee/d4bm00165f-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0bb2/11358866/e5eb01f827c5/d4bm00165f-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0bb2/11358866/32517e37c7c7/d4bm00165f-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0bb2/11358866/a507c6b5901d/d4bm00165f-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0bb2/11358866/aeedb7f2e550/d4bm00165f-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0bb2/11358866/414e86af69c3/d4bm00165f-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0bb2/11358866/4f5f33f0e595/d4bm00165f-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0bb2/11358866/2d14f8686fee/d4bm00165f-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0bb2/11358866/e5eb01f827c5/d4bm00165f-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0bb2/11358866/32517e37c7c7/d4bm00165f-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0bb2/11358866/a507c6b5901d/d4bm00165f-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0bb2/11358866/aeedb7f2e550/d4bm00165f-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0bb2/11358866/414e86af69c3/d4bm00165f-f7.jpg

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