Exact(6)
Screening and selection of phage displayed material binding peptides has attracted great interest because of their use for development of hybrid materials with multiple functionalities.
These peptides contain at least one material binding sequence and at least one biologically active sequence and thus are termed, "Interfacial Biomaterials" (IFBMs).
The methods for immobilizing whole cells include entrapment by an inert support like gel, adsorption by an inert support like ion exchange material, binding via immobilized biological macromolecules or attachment to the activated surface of the matrix, and autoimmobilization.
This strategy of combining cell and material binding phage display derived peptides is broadly applicable to a variety of systems requiring targeted adhesion of specific cell populations, and may be generalized to the engineering of any adhesion surface.
For the adsorption of the adsorbates onto the adsorbent in aqueous solution, two diffusion steps are absolutely necessary: (1) mass transfer from water to the adsorbent surface across the boundary layer (film diffusion) and (2) diffusion of adsorbate molecules within the pores of material, binding the pores and capillary spaces (intraparticle diffusion) [42].
A number of genus-specific mechanisms enable sibling skeletons to be held together at their abbasal surfaces, including a zig-zag design of the basal ring achieved via apical structure, strut attachment and pike rotation (in Distephanus and Dictyocha), and the presence of organic material binding the generally planar basal rings (in Octactis).
Similar(53)
The temperature dependence of thermal expansion coefficients gives information on the intrinsic properties of materials (binding forces, lattice dynamics, band and crystal structure, degree of crystallinity, specific heat, and phase transitions).
In concert, these biopolymers form the complex networks comprising the plant cell wall, where cellulose constitutes the core of the relatively rigid microfibrils and other cell wall polymers form 'matrixing' materials binding the system into a kind of 'liquid polymer crystal'.
Furthermore, I introduced the material-binding peptides that are capable of direct recognition of the target materials.
Here we propose a new method for immobilizing cytokines on material surfaces: a material-binding artificial peptide is used to mediate reversible interaction between the cytokine and the material surface.
Preparation and immobilization strategies for recombinant antibody fragments linked to material-binding peptides (polystyrene-binding peptides (PS-tags) and poly (methyl methacrylate -binding peptide (Pmethacrylate -bindingus here, and are based on the enhancement of sensitivity and a reduction in the peptideion costs of ligand antibodies.
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