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Biology subjects

Ruffine, V.

Publications and source records attributed to Ruffine, V..

2 recordsLinked to original sources

A protein-DNA surface hydrogel mechanically protects the cell nucleus

The nuclear envelope protects the genome from mechanical stress during processes such as migration, division, and compression1-6, but how it buffers forces at the scale of DNA remains unclear. Here, we utilize optical tweezers to show that a multivalent protein-DNA co-condensate containing the nuclear envelope protein LEM27,8 and the DNA-binding protein BAF 9,10 shield DNA beyond its melting point at 65 pN11. Under load, their collective assembly induces an unconventional DNA stiffening effect that provides mechanical reinforcement, dependent on the intrinsically disordered region (IDR) of LEM2. At the nuclear surface, these components form an elastic surface hydrogel in which LEM2 IDR-IDR interactions contract the surface hydrogel relative to its relaxed state, introducing a pre-stress in the lamin network. Inside cells, this surface hydrogel model can recapitulate elastic properties of the nuclear envelope measured via AFM indentation experiments as well as nuclear morphology, using parameters obtained at the molecular scale by use of optical tweezers. Disruption of the surface hydrogel increases DNA damage and micronuclei formation during nuclear deformation. These findings reveal a load-bearing, mesoscale surface hydrogel that reinforces the nucleus and expands the functional repertoire of biomolecular condensates to include DNA protection under mechanical stress.

biophysics↗

Influence of metal cations on the viscoelastic properties of Escherichia coli biofilms

Biofilms frequently cause complications in various areas of human life, e.g. in medicine and in the food industry. More recently, biofilms are discussed as new types of living materials with tuneable mechanical properties. In particular, Escherichia coli produces a matrix composed of amyloid-forming curli and phosphoethanolamine-modified cellulose fibres in response to suboptimal environmental conditions. It is currently unknown how the interaction between these fibres contributes to the overall mechanical properties of the formed biofilms and if extrinsic control parameters can be utilized to manipulate these properties. Using shear rheology, we show that biofilms formed by the E. coli K-12 strain AR3110 stiffen by a factor of two when exposed to the trivalent metal cations Al(III) and Fe(III) while no such response is observed for the bivalent cations Zn(II) and Ca(II). Strains producing only one matrix component did not show any stiffening response to either cation or even a small softening. No stiffening response was further observed when strains producing only one type of fibre were co-cultured or simply mixed after biofilm growth. These results suggest that the E. coli biofilm matrix is a uniquely structured composite material when both matrix fibres are produced from the same bacterium. While the exact interaction mechanism between curli, phosphoethanolamine-modified cellulose and trivalent metal cations is currently not known, our results highlight the potential of using extrinsic parameters to understand and control the interplay between biofilm structure and mechanical properties. This will ultimately aid the development of better strategies for controlling biofilm growth. Table of Contents Graphic O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=109 SRC="FIGDIR/small/510089v1_ufig1.gif" ALT="Figure 1"> View larger version (39K): org.highwire.dtl.DTLVardef@12fdd08org.highwire.dtl.DTLVardef@1583efborg.highwire.dtl.DTLVardef@8ef241org.highwire.dtl.DTLVardef@c28dca_HPS_FORMAT_FIGEXP M_FIG C_FIG

biochemistry↗