Abstract
We designed and synthesized a series of 2’-deoxyribonucleoside triphosphates (dNTPs) bearing various lipid moieties. Fatty acid- and cholesterol-modified dNTPs proved to be substrates for KOD XL DNA polymerase in primer extension reactions. They were also mutually compatible for simultaneous multiple incorporations into the DNA strand. The methodology of enzymatic synthesis opened a pathway to diverse structurally unique lipid ON probes containing one or more lipid units. We studied interactions of such probes with the plasma membranes of live cells. Employing rational design, we found a series of lipid ONs with enhanced efficiency of the membrane anchoring. In membrane stability of multiply modified ONs was superior to that of commonly studied ON analogues, in which a single cholesterol molecule is typically tethered to the thread end. Notably, some of the probes were detected at the cell surface even after 24 h upon removal of the probe solution. Such effect was general to several studied cell lines.
Supplementary materials
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Supplementary Information
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Detailed experimental part, methods, characterization of compounds, additional gels etc.
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