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It is usual to assume that aptamers selected against tumor cell lines bind to surface proteins.
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We suggest that, as LTA is released from the membrane, some of it is bound to surface proteins, but a large portion of the released LTA transits the surface into the culture medium.
This concept is supported by the finding that the amount of LTA bound to surface proteins and the amount of LTA released into the culture media is directly related to the amount of membrane-bound LTA (Fig. 6).
Thus, the membrane-bound LTA has no direct impact on hydrophobicity or biofilms other than serving as a reservoir for LTA that is released into the media or bound to surface proteins.
Isogenic mutants defective in expression of emm, mrp, enn, and/or spa genes of eight different serotypes and their parental strains were tested for differences in LTA bound to surface proteins, LTA released into the culture media, and membrane-bound LTA.
These proteins bind to surface receptors like LRP5/6 and frizzled proteins on the surface of mesenchymal cells, leading to signaling through β-catenin, which translocates to the nucleus and activated genes involved in bone formation.
ABT-737 competitively binds to surface hydrophobic grooves of anti-apoptotic proteins of Bcl-2 family, counteracting their protective effect.
Based on our results it is possible to speculate that the interaction occurred among substances contained in F1 is virus-nonspecific, since it has been described that, for example, flavonoids have the ability to bind to viral surface proteins and thus prevent the infection [ 35].
Alternatively, ATBC may bind to surfaces between the proteins or between them and DNA, but it does not seem to intercalate in DNA.
Understanding how pathogens bind to cell surface proteins can lead to the design of novel carbohydrate-based drugs and diagnostic and therapeutic agents.
PRO 2000 has a negative charge, and researchers hoped it would bind to HIV surface proteins that have a positive charge, blocking the virus's ability to infect cells.
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