TY - JOUR
T1 - Effect of Divalent Cations on the Structure and Mechanics of Vimentin Intermediate Filaments
AU - Wu, Huayin
AU - Shen, Yinan
AU - Wang, Dianzhuo
AU - Herrmann, Harald
AU - Goldman, Robert D.
AU - Weitz, David A.
N1 - Funding Information:
R.D.G. and D.A.W. were supported by National Institute of Health Grant 2P01GM096971-06 . D.A.W. was also supported by National Science Foundation Grant DMR-1708729 . H.H. was supported by the German Research Foundation ( HE-1853/11-1 ). Y.S. was supported by the NSF-Simons Center for Mathematical and Statistical Analysis of Biology at Harvard ( NSF Award no. 1764269 ) and the Harvard Quantitative Biology Initiative . This work was performed in part at the Harvard University Center for Nanoscale Systems, a member of the National Nanotechnology Coordinated Infrastructure Network, which is supported by the NSF under NSF Award no. 1541959 .
Funding Information:
We thank P. Janmey and S. K?ster for helpful discussions. We also thank T. Wedig, S. Stoilova-McPhie, C. Marks, and D. Bell for help with imaging. R.D.G. and D.A.W. were supported by National Institute of Health Grant 2P01GM096971-06. D.A.W. was also supported by National Science Foundation Grant DMR-1708729. H.H. was supported by the German Research Foundation (HE-1853/11-1). Y.S. was supported by the NSF-Simons Center for Mathematical and Statistical Analysis of Biology at Harvard (NSF Award no. 1764269) and the Harvard Quantitative Biology Initiative. This work was performed in part at the Harvard University Center for Nanoscale Systems, a member of the National Nanotechnology Coordinated Infrastructure Network, which is supported by the NSF under NSF Award no. 1541959.
Publisher Copyright:
© 2020 Biophysical Society
PY - 2020/7/7
Y1 - 2020/7/7
N2 - Divalent cations behave as effective cross-linkers of intermediate filaments (IFs) such as vimentin IF (VIF). These interactions have been mostly attributed to their multivalency. However, ion-protein interactions often depend on the ion species, and these effects have not been widely studied in IFs. Here, we investigate the effects of two biologically important divalent cations, Zn2+ and Ca2+, on VIF network structure and mechanics in vitro. We find that the network structure is unperturbed at micromolar Zn2+ concentrations, but strong bundle formation is observed at a concentration of 100 μM. Microrheological measurements show that network stiffness increases with cation concentration. However, bundling of filaments softens the network. This trend also holds for VIF networks formed in the presence of Ca2+, but remarkably, a concentration of Ca2+ that is two orders higher is needed to achieve the same effect as with Zn2+, which suggests the importance of salt-protein interactions as described by the Hofmeister effect. Furthermore, we find evidence of competitive binding between the two divalent ion species. Hence, specific interactions between VIFs and divalent cations are likely to be an important mechanism by which cells can control their cytoplasmic mechanics.
AB - Divalent cations behave as effective cross-linkers of intermediate filaments (IFs) such as vimentin IF (VIF). These interactions have been mostly attributed to their multivalency. However, ion-protein interactions often depend on the ion species, and these effects have not been widely studied in IFs. Here, we investigate the effects of two biologically important divalent cations, Zn2+ and Ca2+, on VIF network structure and mechanics in vitro. We find that the network structure is unperturbed at micromolar Zn2+ concentrations, but strong bundle formation is observed at a concentration of 100 μM. Microrheological measurements show that network stiffness increases with cation concentration. However, bundling of filaments softens the network. This trend also holds for VIF networks formed in the presence of Ca2+, but remarkably, a concentration of Ca2+ that is two orders higher is needed to achieve the same effect as with Zn2+, which suggests the importance of salt-protein interactions as described by the Hofmeister effect. Furthermore, we find evidence of competitive binding between the two divalent ion species. Hence, specific interactions between VIFs and divalent cations are likely to be an important mechanism by which cells can control their cytoplasmic mechanics.
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U2 - 10.1016/j.bpj.2020.05.016
DO - 10.1016/j.bpj.2020.05.016
M3 - Article
C2 - 32521238
AN - SCOPUS:85086150471
SN - 0006-3495
VL - 119
SP - 55
EP - 64
JO - Biophysical Journal
JF - Biophysical Journal
IS - 1
ER -