287 research outputs found

    Fluctuating Nonlinear Spring Model of Mechanical Deformation of Biological Particles

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    We present a new theory for modeling forced indentation spectral lineshapes of biological particles, which considers non-linear Hertzian deformation due to an indenter-particle physical contact and bending deformations of curved beams modeling the particle structure. The bending of beams beyond the critical point triggers the particle dynamic transition to the collapsed state, an extreme event leading to the catastrophic force drop as observed in the force (F)-deformation (X) spectra. The theory interprets fine features of the spectra: the slope of the FX curves and the position of force-peak signal, in terms of mechanical characteristics --- the Young's moduli for Hertzian and bending deformations E_H and E_b, and the probability distribution of the maximum strength with the strength of the strongest beam F_b^* and the beams' failure rate m. The theory is applied to successfully characterize the FXFX curves for spherical virus particles --- CCMV, TrV, and AdV

    Repeat Subglacial Lake Drainage and Filling beneath Thwaites Glacier

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    Physics of viral dynamics

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    Viral capsids are often regarded as inert structural units, but in actuality they display fascinating dynamics during different stages of their life cycle. With the advent of single-particle approaches and high-resolution techniques, it is now possible to scrutinize viral dynamics during and after their assembly and during the subsequent development pathway into infectious viruses. In this Review, the focus is on the dynamical properties of viruses, the different physical virology techniques that are being used to study them, and the physical concepts that have been developed to describe viral dynamics

    Mechanical Characterization of Liposomes and Extracellular Vesicles, a Protocol

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    Both natural as well as artificial vesicles are of tremendous interest in biology and nanomedicine. Small vesicles (<200 nm) perform essential functions in cell biology and artificial vesicles (liposomes) are used as drug delivery vehicles. Atomic Force Microscopy (AFM) is a powerful technique to study the structural properties of these vesicles. AFM is a well-established technique for imaging at nanometer resolution and for mechanical measurements under physiological conditions. Here, we describe the procedure of AFM imaging and force spectroscopy on small vesicles. We discuss how to image vesicles with minimal structural disturbance, and how to analyze the data for accurate size and shape measurements. In addition, we describe the procedure for performing nanoindentations on vesicles and the subsequent data analysis including mechanical models used for data interpretation

    Calibrating bead displacements in optical tweezers using acousto-optic deflectors

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    Displacements of optically trapped particles are often recorded using back-focal-plane interferometry. In order to calibrate the detector signals to displacements of the trapped object, several approaches are available. One often relies either on scanning a fixed bead across the waist of the laser beam or on analyzing the power spectrum of movements of the trapped bead. Here, we introduce an alternative method to perform this calibration. The method consists of very rapidly scanning the laser beam across the solvent-immersed, trapped bead using acousto-optic deflectors while recording the detector signals. It does not require any knowledge of solvent viscosity and bead diameter, and works in all types of samples, viscous or viscoelastic. Moreover, it is performed with the same bead as that used in the actual experiment. This represents marked advantages over established methods. © 2006 American Institute of Physics

    Evolution of surface velocities and ice discharge of Larsen B outlet glaciers from 1995 to 2013

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    We use repeat-pass SAR data to produce detailed maps of surface motion covering the glaciers draining into the former Larsen B ice shelf, Antarctic Peninsula, for different epochs between 1995 and 2013. We combine the velocity maps with estimates of ice thickness to analyze fluctuations of ice discharge. The collapse of the central and northern sections of the ice shelf in 2002 led to a near-immediate acceleration of tributary glaciers as well as of the remnant ice shelf in Scar Inlet. Velocities of the glaciers discharging directly into the ocean remain to date well above the velocities of the pre-collapse period. The response of individual glaciers differs and velocities show significant temporal fluctuations, implying major variations in ice discharge and mass balance as well. Due to reduced velocity and ice thickness the ice discharge of Crane Glacier decreased from 5.02 Gt a−1 in 2007 to 1.72 Gt a−1 in 2013, whereas Hektoria and Green glaciers continue to show large temporal fluctuations in response to successive stages of frontal retreat. The velocity on Scar Inlet ice shelf increased two- to three fold since 1995, with the largest increase in the first years after the break-up of the main section of Larsen B. Flask and Leppard glaciers, the largest tributaries to Scar Inlet ice shelf, accelerated. In 2013 their discharge was 38% and 46%, higher than in 1995

    A single point mutation in precursor protein VI doubles the mechanical strength of human adenovirus

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    Viruses are extensively studied as vectors for vaccine applications and gene therapies. For these applications, understanding the material properties of viruses is crucial for creating optimal functionality. Using atomic force microscopy (AFM) nanoindentation, we studied the mechanical properties of human adenovirus type 5 with the fiber of type 35 (Ad5F35) and compared it to viral capsids with a single point mutation in the protein VI precursor protein (pVI-S28C). Surprisingly, the pVI-S28C mutant turned out to be twice as stiff as the Ad5F35 capsids. We suggest that this major increase in strength is the result of the DNA crosslinking activity of precursor protein VII, as this protein was detected in the pVI-S28C mutant capsids. The infectivity was similar for both capsids, indicating that mutation did not affect the ability of protein VI to lyse the endosomal membrane. This study highlights that it is possible to increase the mechanical stability of a capsid even with a single point mutation while not affecting the viral life cycle. Such insight can help enable the development of more stable vectors for therapeutic applications

    DNA looping by FokI: the impact of twisting and bending rigidity on protein-induced looping dynamics

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    Protein-induced DNA looping is crucial for many genetic processes such as transcription, gene regulation and DNA replication. Here, we use tethered-particle motion to examine the impact of DNA bending and twisting rigidity on loop capture and release, using the restriction endonuclease FokI as a test system. To cleave DNA efficiently, FokI bridges two copies of an asymmetric sequence, invariably aligning the sites in parallel. On account of the fixed alignment, the topology of the DNA loop is set by the orientation of the sites along the DNA. We show that both the separation of the FokI sites and their orientation, altering, respectively, the twisting and the bending of the DNA needed to juxtapose the sites, have profound effects on the dynamics of the looping interaction. Surprisingly, the presence of a nick within the loop does not affect the observed rigidity of the DNA. In contrast, the introduction of a 4-nt gap fully relaxes all of the torque present in the system but does not necessarily enhance loop stability. FokI therefore employs torque to stabilise its DNA-looping interaction by acting as a ‘torsional’ catch bond
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