Department of Materials and Environmental Chemistry, Stockholm University, Stockholm 10691, Sweden.
CNR-ICCOM, Institute of Chemistry of Organometallic Compounds, via Moruzzi 1, Pisa 56124, Italy.
Biomacromolecules. 2024 Jun 10;25(6):3703-3714. doi: 10.1021/acs.biomac.4c00264. Epub 2024 May 28.
As a versatile nanomaterial derived from renewable sources, nanocellulose has attracted considerable attention for its potential applications in various sectors, especially those focused on water treatment and remediation. Here, we have combined atomic force microscopy (AFM) and reactive molecular dynamics (RMD) simulations to characterize the interactions between cellulose nanofibers modified with carboxylate or phosphate groups and the protein foulant model bovine serum albumin (BSA) at pH 3.92, which is close to the isoelectric point of BSA. Colloidal probes were prepared by modification of the AFM probes with the nanofibers, and the nanofiber coating on the AFM tip was for the first time confirmed through fluorescence labeling and confocal optical sectioning. We have found that the wet-state normalized adhesion force is approximately 17.87 ± 8.58 pN/nm for the carboxylated cellulose nanofibers (TOCNF) and about 11.70 ± 2.97 pN/nm for the phosphorylated ones (PCNF) at the studied pH. Moreover, the adsorbed protein partially unfolded at the cellulose interface due to the secondary structure's loss of intramolecular hydrogen bonds. We demonstrate that nanocellulose colloidal probes can be used as a sensitive tool to reveal interactions with BSA at nano and molecular scales and under in situ conditions. RMD simulations helped to gain a molecular- and atomistic-level understanding of the differences between these findings. In the case of PCNF, partially solvated metal ions, preferentially bound to the phosphates, reduced the direct protein-cellulose connections. This understanding can lead to significant advancements in the development of cellulose-based antifouling surfaces and provide crucial insights for expanding the pH range of use and suggesting appropriate recalibrations.
作为一种源自可再生资源的多功能纳米材料,纳米纤维素因其在各个领域的潜在应用而受到广泛关注,尤其是在水处理和修复领域。在这里,我们结合原子力显微镜(AFM)和反应分子动力学(RMD)模拟,研究了在接近牛血清白蛋白(BSA)等电点的 pH 3.92 下,经羧基或磷酸基团改性的纤维素纳米纤维与蛋白质污染物模型牛血清白蛋白(BSA)之间的相互作用。通过对 AFM 探针进行修饰,制备了胶体探针,并首次通过荧光标记和共聚焦光学切片证实了 AFM 尖端上的纳米纤维涂层。我们发现,在研究的 pH 值下,羧基化纤维素纳米纤维(TOCNF)的湿态归一化粘附力约为 17.87 ± 8.58 pN/nm,而磷酸化纤维素纳米纤维(PCNF)的约为 11.70 ± 2.97 pN/nm。此外,由于分子内氢键的丧失,吸附在纤维素界面上的部分蛋白质发生了部分展开。我们证明,纳米纤维素胶体探针可用作一种灵敏的工具,在纳米和分子尺度以及原位条件下揭示与 BSA 的相互作用。RMD 模拟有助于从分子和原子水平上理解这些差异。在 PCNF 的情况下,部分溶剂化的金属离子优先与磷酸根结合,减少了蛋白质与纤维素的直接连接。这种理解可以推动基于纤维素的抗污表面的开发,并为扩大使用 pH 范围和提出适当的重新校准提供关键的见解。