Words similar to uncharged
Example sentences for: uncharged
How can you use “uncharged” in a sentence? Here are some example sentences to help you improve your vocabulary:
They include: (1) sulfate esters of polysaccharides {carrageenan [ 1 16 17 18 19 ] , cellulose sulfate [ 12 13 14 15 ] , and dextran or dextrin sulfate [ 1 2 3 4 5 6 7 8 9 10 11 ] }; (2) aryl sulfonates {poly(naphthalene sulfonate) [ 22 23 24 ] and poly(styrene-4-sulfonate) [ 20 21 ] }; and (3) aliphatic {Carbomer 974P/BufferGel [ 25 26 27 28 29 ] } and aromatic carboxylates {CAP [ 30 31 32 33 34 35 36 37 ] }. The anti-HIV-1 properties of these polymers are expected to depend on their complexation with virus proteins which is likely to occur mainly through the formation of salt linkages or ion pairs between oppositely charged groups on the polymers and virus proteins, respectively [ 56 ] . However, the anti-HIV-1 properties of these polymers may depend not only on their charge density, but also on the characteristics of their uncharged portions, which may be involved in hydrophobic and hydrogen bonding interactions which can elicit profound conformational changes in hydrophobic regions of proteins and cause disassembly of complex proteins consisting of subunits [ 57 ] . For these reasons it is not be expected that all anionic polymers, considered as anti-HIV-1 microbicides, would have similar biological activities.
Based on the normal function of GCN2-like proteins [ 25 ] , these findings suggest that uncharged tRNAs are more prevalent within the cells during this time relative to either growing cells or to cells immediately after removal of the food source.
Because Val and Met are both non-polar amino acids, and Ser and Gly are both polar and uncharged amino acids, those amino acid substitutions between ZAS-N and ZAS-C may result in minor changes in the tertiary structure of the zinc fingers which account for the subtle differences in the DNA binding properties of the ZAS-N and ZAS-C domains.
This difference may possibly be due to the high propensity of the uncharged part of the molecule {poly(naphtalene)} to be involved in hydrophobic interactions.
The results and related considerations are compatible with similar results in purely aqueous solutions [ 12 13 14 ] , and support both the estimated solubility (S o ) of 5.1 × 10-8 M for uncharged UCB (H
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