Tata Institute of Fundamental Research, Hyderabad500046, India.
J Phys Chem Lett. 2022 Jun 23;13(24):5660-5668. doi: 10.1021/acs.jpclett.2c00853. Epub 2022 Jun 16.
To counter the stress of a salt imbalance, the cell often produces low molecular weight osmolytes to resuscitate homeostasis. However, how zwitterionic osmolytes would tune the electrostatic interactions among charged biomacromolecular surfaces under salt stress has eluded mainstream investigations. Here, via combination of molecular simulation and experiment, we demonstrate that a set of zwitterionic osmolytes is able to restore the electrostatic interaction between two negatively charged surfaces that had been masked in the presence of salt. Interestingly, the mechanisms of resurrecting charge interaction under excess salt are revealed to be mutually divergent and osmolyte specific. In particular, glycine is found to competitively desorb the salt ions from the surface via its direct interaction with the surface. On the contrary, TMAO and betaine counteract salt stress by retaining adsorbed cations but partially neutralizing their charge density via ion-mediated interaction. These access to alternative modes of osmolytic actions would provide the cell the required flexibility in combating salt stress.
为了应对盐失衡带来的压力,细胞通常会产生低分子量的渗透物来恢复体内平衡。然而,两性离子渗透物如何在盐胁迫下调节带电生物大分子表面之间的静电相互作用,这一问题一直困扰着主流研究。在这里,我们通过分子模拟和实验的结合,证明了一组两性离子渗透物能够恢复在盐存在下被掩盖的两个带负电荷表面之间的静电相互作用。有趣的是,揭示出在过量盐存在下复活电荷相互作用的机制是相互分歧和渗透物特异性的。具体来说,发现甘氨酸通过与表面的直接相互作用,竞争性地从表面上解吸盐离子。相比之下,TMAO 和甜菜碱通过保留吸附的阳离子并通过离子介导的相互作用部分中和其电荷密度来对抗盐胁迫。这些获得的渗透物作用的替代模式为细胞在抵御盐胁迫时提供了所需的灵活性。