Sentence examples for moieties are added from inspiring English sources

Fullerenes have a highly unsaturated structure and excellent electron-receptor properties, and for these reasons, these molecules particularly water-soluble fullerene derivatives in which hydrophilic group moieties are added to the carbon cage for biological uses—have been investigated extensively as radical scavengers [1].

Glycosyltransferase enzymes catalyze the final reactions in the biosynthesis of SGAs, where different sugar moieties are added to the solanidine aglycone.

Due to these considerations, fluorescent moieties are added to monomer formulation to achieve an amplified, fluorescent signal that correlates with polymer growth.

Intra-cellularly, glutamate moieties are added by folylpolyglutamate synthetase (FPGS) such that MTX is retained within cells as MTX polyglutamates (MTXGlun).

The models, shown schematically in Figure 1, differ with respect to the questions of whether the two E2 E3 pairs act sequentially (A, B) or in concert (C, D), and whether the ubiquitin moieties are added in a stepwise manner (A, C) or transferred en bloc to PCNA (B, D).

On the basis of the electron density interpretation, the inhibitor and glycosylated carbohydrate moieties were added in the complex structure and further refinement was carried out.

A solution of GFP-CVIA, GST-CVIA, or proG-CVIA modified at the C-terminal cysteine with farnesyl (GFP-CVIAf and GST-CVIAf) or propargylfarnesyl (GFP-CVIApf, GST-CVIApf, and proG-CVIApf) moieties was added to individual wells, followed by 0.5 mM CuSO4, 50 μM TBTA, and 0.5 mM TCEP (final volume 10 μL).

Alkyne-functionalized pyrene with a photocleavable 2-nitrobenzyl moiety was added to the PEO-b-PAzHEMA backbone via click chemistry to produce the desired block copolymer with high fidelity.

Initially a farnesyl moiety is added to the cysteine by farnesyltransferase, followed by cleavage of the last three amino acids (-aaXing) by either Rce1 or ZmpSte24.

A single 39 adenosine moiety was added to the cDNA using Klenow exo and dATP.

Since no structural model of quinupristin was available, virginiamycin S was used as an initial model; the quinuclidinylthio-moiety was added manually and subsequently minimized.