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研究镧系元素与来自 Lanmodulin 的 EF-手环 I 的表面结合亲和肽的结合。

Investigation of Rare Earth Element Binding to a Surface-Bound Affinity Peptide Derived from EF-Hand Loop I of Lanmodulin.

机构信息

Department of Chemical and Biomolecular Engineering, Case Western Reserve University, Cleveland, Ohio 44106, United States.

School of Chemical and Biomolecular Engineering, Georgia Institute of Technology, Atlanta, Georgia 30332, United States.

出版信息

ACS Appl Mater Interfaces. 2024 Apr 3;16(13):16912-16926. doi: 10.1021/acsami.3c17565. Epub 2024 Mar 25.

Abstract

Bioinspired strategies have been given extensive attention for the recovery of rare earth elements (REEs) from waste streams because of their high selectivity, regeneration potential, and sustainability as well as low cost. Lanmodulin protein is an emerging biotechnology that is highly selective for REE binding. Mimicking lanmodulin with shorter peptides is advantageous because they are simpler and potentially easier to manipulate and optimize. Lanmodulin-derived peptides have been found to bind REEs, but their properties have not been explored when immobilized on solid substrates, which is required for many advanced separation technologies. Here, two peptides, LanM1 and scrambled LanM1, are designed from the EF-hand loop 1 of lanmodulin and investigated for their binding affinity toward different REEs when surface-bound. First, the ability of LanM1 to bind REEs was confirmed and characterized in solution using circular dichroism (CD), nuclear magnetic resonance (NMR), and molecular dynamics (MD) simulations for Ce(III) ions. Isothermal titration calorimetry (ITC) was used to further analyze the binding of the LanM1 to Ce(III), Nd(III), Eu(III), and Y(III) ions and in low-pH conditions. The performance of the immobilized peptides on a model gold surface was examined using a quartz crystal microbalance with dissipation (QCM-D). The studies show that the LanM1 peptide has a stronger REE binding affinity than that of scrambled LanM1 when in solution and when immobilized on a gold surface. QCM-D data were fit to the Langmuir adsorption model to estimate the surface-bound dissociation constant () of LanM1 with Ce(III) and Nd(III). The results indicate that LanM1 peptides maintain a high affinity for REEs when immobilized, and surface-bound LanM1 has no affinity for potential competitor calcium and copper ions. The utility of surface-bound LanM1 peptides was further demonstrated by immobilizing them to gold nanoparticles (GNPs) and capturing REEs from solution in experiments utilizing an Arsenazo III-based colorimetric dye displacement assay and ultraviolet-visible (UV-vis) spectrophotometry. The saturated adsorption capacity of GNPs was estimated to be around 3.5 μmol REE/g for Ce(III), Nd(III), Eu(III), and Y(III) ions, with no binding of non-REE Ca(II) ions observed.

摘要

生物启发策略因其高选择性、再生潜力和可持续性以及低成本而受到广泛关注,可用于从废物流中回收稀土元素 (REEs)。Lanmodulin 蛋白是一种新兴生物技术,对 REE 具有高度选择性。用更短的肽模拟 Lanmodulin 具有优势,因为它们更简单,并且可能更容易操作和优化。已经发现 Lanmodulin 衍生肽与 REE 结合,但尚未研究它们在固定在固体基质上时的性质,这是许多先进分离技术所必需的。在这里,根据 Lanmodulin 的 EF 手 loop1 设计了两个肽,LanM1 和 scrambled LanM1,并研究了它们在表面结合时对不同 REE 的结合亲和力。首先,使用圆二色性 (CD)、核磁共振 (NMR) 和分子动力学 (MD) 模拟证实并表征了 LanM1 结合 Ce(III)离子的能力。等温滴定量热法 (ITC) 用于进一步分析 LanM1 与 Ce(III)、Nd(III)、Eu(III)和 Y(III)离子的结合,并在低 pH 条件下进行分析。使用石英晶体微天平与耗散 (QCM-D) 研究了固定在模型金表面上的肽的性能。研究表明,在溶液中和固定在金表面上时,LanM1 肽对 REE 的结合亲和力强于 scrambled LanM1。QCM-D 数据拟合到 Langmuir 吸附模型,以估计 LanM1 与 Ce(III)和 Nd(III)的表面结合离解常数 (Kd)。结果表明,固定化后 LanM1 肽对 REE 保持高亲和力,而固定化表面的 LanM1 对潜在竞争的钙和铜离子没有亲和力。通过将它们固定在金纳米颗粒 (GNP) 上来进一步证明表面固定化 LanM1 肽的用途,并在利用基于 arsenazo III 的比色染料置换测定法和紫外可见 (UV-vis) 分光光度法的实验中从溶液中捕获 REE。GNP 的饱和吸附容量估计约为 3.5 μmol REE/g,用于 Ce(III)、Nd(III)、Eu(III)和 Y(III)离子,未观察到非 REE Ca(II)离子的结合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5217/10995902/1c1838a67681/am3c17565_0001.jpg

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