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Further, thermodynamic changes arising from small differences between ligands binding to individual proteins are relatively large and, in general, uncorrelated with changes in solvation, suggesting that trends identified across widely differing proteins are of limited use in explaining or predicting the effects of ligand modifications.
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This includes screening for co-factors, substrates, differing protein or nucleotide partners or small molecule inhibitors, to more fully characterize the variations within assembly states and key conformational changes.
By applying gene expression levels on such a scale, and by adhering to such constraints, it is hoped that effects such as experimental error, differing protein translation rates, differing transcript and protein stabilities, and differing enzymatic activities, will be reduced.
Coordinates of significantly differing protein spots (p≤0.05 with FDR correction, r a t i o≥|3| when comparing both treatments) were transferred to a pick list for further processing.
Mass spectrometry reveals differing protein interactions between DDB1 and distinct DCAFs, the substrate recognizing components of the E3 complex, between cell types.
Therefore, the hypoxia sensing scaffold signal would behave the same regardless of the tissue, since the physiological conditions (salinity, pH) are similar across tissue types while differing protein content does not affect the signal.
Therefore, the results indicate that the indices of solvent sensitivity (solvatochromism) and conformational freedom (viscosity) can be utilized as predictive determinants for achieving superior LCOs for spectral separation of differing protein aggregates.
Most of the differed proteins were involved in actin dynamics, cell adhesion, as well as G-protein signaling pathways.
Since tissue specimens contain various types of cells, where the expressions of target proteins differ, protein assay results become hard to interpret and may even be misleading.
The specificities of these two ligands differ; Protein S was reported to be a specific agonist for TYRO3, while in cells that co-express TYRO3, Protein S is also a potent MERTK agonist [ 7].
CFPS conditions differ from protein to protein to account for protein complexity, folding, and post-translational modifications.
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