Renzer Galit, Eufemio Rosemary J, Schwidetzky Ralph, Fröhlich-Nowoisky Janine, Bonn Mischa, Meister Konrad
Department for Molecular Spectroscopy, Max Planck Institute for Polymer Research, Ackermannweg 10, 55128 Mainz, Germany.
Department of Chemistry and Biochemistry, Boise State University, 2133 Cesar Chavez, Boise, 83725 Idaho, United States.
J Phys Chem C Nanomater Interfaces. 2024 Dec 5;128(50):21604-21608. doi: 10.1021/acs.jpcc.4c07422. eCollection 2024 Dec 19.
Ice-nucleating proteins (INPs) from bacteria like are among the most effective ice nucleators known. However, large INP aggregates with maximum ice nucleation activity (at approximately -2 °C) typically account for less than 1% of the overall ice nucleation activity in bacterial samples. This study demonstrates that polyols significantly enhance the assembly of INPs into large aggregates, dramatically improving bacterial ice nucleation efficiency. Simple compounds like polyvinyl alcohol increased the abundance of large INP aggregates by a factor of 100. This remarkable boost in ice nucleation efficiency is attributed to the stabilization of INP aggregates through membrane-polyol interactions that stabilize INP interactions and reduce structural fluctuations. The ability to regulate the abundance of large INP aggregates in bacterial ice nucleators enables fine-tuning ice nucleation processes at much lower concentrations for specific biomedical and technological purposes.
诸如来自细菌的冰核蛋白(INPs)是已知最有效的冰核剂之一。然而,具有最大冰核活性(约在-2°C)的大型INP聚集体通常在细菌样品的总体冰核活性中占比不到1%。本研究表明,多元醇显著增强了INPs组装成大型聚集体的过程,极大地提高了细菌的冰核效率。像聚乙烯醇这样的简单化合物使大型INP聚集体的丰度增加了100倍。冰核效率的这一显著提高归因于通过膜 - 多元醇相互作用对INP聚集体的稳定作用,这种相互作用稳定了INP相互作用并减少了结构波动。调节细菌冰核剂中大型INP聚集体丰度的能力能够在更低浓度下针对特定的生物医学和技术目的对冰核过程进行微调。