4.8 Article

Sink or Swim: Ions and Organics at the Ice-Air Interface

期刊

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 139, 期 29, 页码 10095-10103

出版社

AMER CHEMICAL SOC
DOI: 10.1021/jacs.7b05233

关键词

-

资金

  1. National Science Foundation [CHE-1305427]
  2. University of Utah through an Undergraduate Research Opportunity Fellowship

向作者/读者索取更多资源

The ice air interface is an important locus of environmental chemical reactions. The structure and dynamics of the ice surface impact the uptake of trace gases and kinetics of reactions in the atmosphere and snowpack. At tropospheric temperatures, the ice surface is partially premelted. Experiments indicate that ions increase the liquidity of the ice surface but hydrophilic organics do not. However, it is not yet known the extent of the perturbation solutes induce at the ice surface and what is the role of the disordered liquid-like layer in modulating the interaction between solutes and their mobility and aggregation at the ice surface. Here we use large-scale molecular simulations to investigate the effect of ions and glyoxal, one of the most abundant oxygenated volatile organic compounds in the atmosphere, on the structure, dynamics, and solvation properties of the ice surface. We find that the premelted surface of ice has unique solvation properties, different from those of liquid water. The increase in surface liquidity resulting from the hydration of ions leads to a water-mediated attraction of ions at the ice surface. Glyoxal molecules, on the other hand, perturb only slightly the surface of ice and do not experience water-driven attraction. They nonetheless accumulate as dry agglomerates at the ice surface, driven by direct interactions between the organic molecules. The enhanced attraction and clustering of ions and organics at the ice surface may play a significant role in modulating the mechanism and rate of heterogeneous chemical reactions occurring at the surface of atmospheric ice particles.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

Article Chemistry, Multidisciplinary

What Determines the Ice Polymorph in Clouds?

Arpa Hudait, Valeria Molinero

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2016)

Article Chemistry, Physical

Free energy contributions and structural characterization of stacking disordered ices

Arpa Hudait, Siwei Qiu, Laura Lupi, Valeria Molinero

PHYSICAL CHEMISTRY CHEMICAL PHYSICS (2016)

Article Chemistry, Multidisciplinary

Ice Nucleation Efficiency of Hydroxylated Organic Surfaces Is Controlled by Their Structural Fluctuations and Mismatch to Ice

Yuqing Qiu, Nathan Odendahl, Arpa Hudait, Ryan Mason, Allan K. Bertram, Francesco Paesani, Paul J. DeMott, Valeria Molinero

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2017)

Article Multidisciplinary Sciences

Role of stacking disorder in ice nucleation

Laura Lupi, Arpa Hudait, Baron Peters, Michael Grunwald, Ryan Gotchy Mullen, Andrew H. Nguyen, Valeria Molinero

NATURE (2017)

Article Chemistry, Multidisciplinary

Ice-Nucleating and Antifreeze Proteins Recognize Ice through a Diversity of Anchored Clathrate and Ice-like Motifs

Arpa Hudait, Nathan Odendahl, Yuqing Qiu, Francesco Paesani, Valeria Molinero

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2018)

Article Multidisciplinary Sciences

Preordering of water is not needed for ice recognition by hyperactive antifreeze proteins

Arpa Hudait, Daniel R. Moberg, Yuqing Qiu, Nathan Odendahl, Francesco Paesani, Valeria Molinero

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2018)

Article Chemistry, Multidisciplinary

Ice Crystallization in Ultrafine Water-Salt Aerosols: Nucleation, Ice-Solution Equilibrium, and Internal Structure

Arpa Hudait, Valeria Molinero

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2014)

Article Chemistry, Multidisciplinary

Heterogeneous Nucleation of Ice on Carbon Surfaces

Laura Lupi, Arpa Hudait, Valeria Molinero

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2014)

Article Chemistry, Multidisciplinary

How Size and Aggregation of Ice-Binding Proteins Control Their Ice Nucleation Efficiency

Yuqing Qiu, Arpa Hudait, Valeria Molinero

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2019)

Article Chemistry, Multidisciplinary

Hydrogen-Bonding and Hydrophobic Groups Contribute Equally to the Binding of Hyperactive Antifreeze and Ice-Nucleating Proteins to Ice

Arpa Hudait, Yuqing Qiu, Nathan Odendahl, Valeria Molinero

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2019)

Article Multidisciplinary Sciences

The end of ice I

Daniel R. Moberg, Daniel Becker, Christoph W. Dierking, Florian Zurheide, Bernhard Bandow, Udo Buck, Arpa Hudait, Valeria Molinero, Francesco Paesani, Thomas Zeuch

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2019)

Article Biochemistry & Molecular Biology

A helical assembly of human ESCRT-I scaffolds reverse-topology membrane scission

Thomas G. Flower, Yoshinori Takahashi, Arpa Hudait, Kevin Rose, Nicholas Tjahjono, Alexander J. Pak, Adam L. Yokom, Xinwen Liang, Hong-Gang Wang, Fadila Bouamr, Gregory A. Voth, James H. Hurley

NATURE STRUCTURAL & MOLECULAR BIOLOGY (2020)

Article Multidisciplinary Sciences

Prion-like low complexity regions enable avid virus-host interactions during HIV-1 infection

Guochao Wei, Naseer Iqbal, Valentine V. Courouble, Ashwanth C. Francis, Parmit K. Singh, Arpa Hudait, Arun S. Annamalai, Stephanie Bester, Szu-Wei Huang, Nikoloz Shkriabai, Lorenzo Briganti, Reed Haney, Vineet N. KewalRamani, Gregory A. Voth, Alan N. Engelman, Gregory B. Melikyan, Patrick R. Griffin, Francisco Asturias, Mamuka Kvaratskhelia

Summary: This study highlights the importance of prion-like low complexity domains in binding and increasing the avidity when interacting with viral capsid, through structural, biochemical, and virological assays.

NATURE COMMUNICATIONS (2022)

Article Biophysics

Dynamics of upstream ESCRT organization at the HIV-1 budding site

Arpa Hudait, James H. Hurley, Gregory A. Voth

Summary: In the late stages of the HIV-1 life cycle, the membrane localization and self-assembly of Gag polyproteins induce membrane deformation and budding. The release of the virion requires the interaction between Gag lattice and ESCRT machinery at the viral budding site, followed by the assembly of downstream ESCRT-III factors. However, the molecular details of upstream ESCRT assembly dynamics remain unclear. In this study, molecular simulations were used to investigate the interactions between Gag, ESCRT-I, ESCRT-II, and membrane, revealing the mechanisms by which upstream ESCRTs assemble at the viral budding site.

BIOPHYSICAL JOURNAL (2023)

暂无数据