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Their physicochemical properties were investigated extensively as models of membrane morphology.
New models of membrane systems need to be simulated on complex hardware systems to provide a valuable feedback to biologists.
Models of membrane reactors (MRs) and catalytic membranes are presented by taking into account the advantages of the separation provided by the membranes.
In most proposed models of membrane fusion it is postulated that the S1 domain or analogous receptor binding domains dissociate from the spike during the membrane fusion process.
Thus, they perform poorly when applied to models of membrane proteins.
In turn, these improved alignments lead to better structural models of membrane proteins.
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However, advances in micro/nanofabrication have resulted in more realistic synthetic models of membrane-cytoskeleton interactions that can help uncover the design rules responsible for biological membrane formation and organization.
Two types of analysis have been conducted for all representative models of membranes.
Here, we systematically assessed the electrostatic forces between SNARE complex, auxiliary proteins and fusing membranes by the nonlinear Poisson-Boltzmann equation using explicit models of membranes and proteins.
A number of simplified models of membranes such as liposomes, black lipid membranes, or supported bilayers have been used to study the interactions of antimicrobial peptides, bacterial toxins, and drug-delivery vehicles, as well as to understand the physicochemical properties of membranes in nature.
The pore widths of 0.6, 0.64, 0.728, and 1.336 nm are selected as models of sieving membrane, monolayer adsorbed membrane, optimum membrane, and bilayer adsorbed membrane, respectively.
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