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Journal ArticleDOI

Differences between non-specific and bio-specific, and between equilibrium and non-equilibrium, interactions in biological systems.

TLDR
It is suggested that the major theoretical challenge is to establish manageable theories or models that can describe the spatial and time evolution of systems consisting of different molecules subject to certain starting conditions or energy inputs.
Abstract
Biological interactions are ‘processes’ 331Intermolecular forces involved 332Synergy between different forces occurring at different locations 333Non-equilibrium, rate and time-dependent interactions 335Reversible and irreversible interactions 337The interaction forces between biological molecules and surfaces are much more complex than those between non-biological molecules or surfaces, such as colloidal particle surfaces. This complexity is due to a number of factors: (i) the simultaneous involvement of many different molecules and different non-covalent forces – van der Waals, electrostatic, solvation (hydration, hydrophobic), steric, entropic and ‘specific’, and (ii) the flexibility of biological macromolecules and fluidity of membranes. Biological interactions are better thought of as ‘processes’ that evolve in space and time and, under physiological conditions, involve a continuous input of energy. Such systems are, therefore, not at thermodynamic equilibrium, or even tending towards equilibrium. Recent surface forces apparatus (SFA) and atomic force microscopy (AFM) measurements on supported model membrane systems (protein-containing lipid bilayers) illustrate these effects. It is suggested that the major theoretical challenge is to establish manageable theories or models that can describe the spatial and time evolution of systems consisting of different molecules subject to certain starting conditions or energy inputs.

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Journal ArticleDOI

Interaction of nanoparticles with lipid membrane

TL;DR: A nanoscale range of surface feature curvatures where lipid membranes lose integrity and form pores has been found experimentally, providing essential information for the understanding of nanoparticle-lipid membrane interaction, cytotoxicity, preparation of biomolecular templates and supported lipid membranes on rough and patterned surfaces.
Journal ArticleDOI

Microfluidic-based biosensors toward point-of-care detection of nucleic acids and proteins

TL;DR: The merger of microfluidics and advanced biosensor technologies offers new promises for POC diagnostics, including high-throughput analysis, portability and disposability, but this merger also imposes technological challenges on biosensors, such as high sensitivity and selectivity requirements with sample volumes orders of magnitude smaller than those of conventional practices.
Journal ArticleDOI

Molecular aspects of boundary lubrication by human lubricin: effect of disulfide bonds and enzymatic digestion.

TL;DR: The necessary condition for LUB to be a good lubricant is that the protein be adsorbed to the surface via its terminals, leaving the central mucin domain free to form a low-friction, surface-protecting layer, and the results suggest that this "end-anchoring" has to be strong enough to impart the layer a sufficient resistance to shear, but without excessively restricting the conformational freedom of the adsorbing proteins.
Journal ArticleDOI

Application of atomic force microscopy in bacterial research.

TL;DR: This review presents the fascinating options offered by the rapid advances in AFM with emphasizes on bacterial research and provides a background for the exciting research articles to follow.
Journal ArticleDOI

Interaction of Lipid Membrane with Nanostructured Surfaces

TL;DR: The study found that the lipid membrane conformed to the substrate with surface structures of dimensions less than 1.2 nm without losing the membrane integrity, providing a new approach for patterning supported lipid membranes with well-defined features in the 1-22 nm range.
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