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31.
The design of single-stranded nucleic acid knots 总被引:1,自引:0,他引:1
Nadrian C. Seeman 《Molecular Engineering》1992,2(3):297-307
A general strategy is described for the synthesis of single-stranded nucleic acid knots. Control of nucleic acid sequence is used to direct the formation of secondary structures that produce the target topology. The key feature of the strategy is the equation of a half-turn of double helical DNA or RNA with a node in a knot. By forming nodes from complementary DNA sequences, it appears possible to direct the assembly of any simple knot. Stabilization of individual nodes may be achieved by constructing them from long regions containing both B-DNA and Z-DNA. Control over the braiding of DNA that acts as a link between node-forming domains can be realized by condensing the nodes into well-defined DNA structures, such as extended domains of linear duplex, branched junctions, antijunctions or mesojunctions. Further topological control may be derived from the pairing of linker regions to complementary single-stranded molecules, thereby preventing them from braiding in an undesirable fashion. 相似文献
32.
33.
34.
Lawrence D. Mayer Marcel B. Bally Michael J. Hope Pieter R. Cullis 《Chemistry and physics of lipids》1986,40(2-4):333-345
As a prerequisite for the use of liposomes for delivery of biologically active agents, techniques are required for the efficient and rapid entrapment of such agents in liposomes. Here we review the variety of procedures available for trapping hydrophilic and hydrophobic compounds. Considerations which are addressed include factors influencing the choice of a particular liposomal system and techniques for the passive entrapment of drugs in multilamellar vesicles and unilamellar vesicles. Attention is also paid to active trapping procedures relying on the presence of (negatively) charged lipid or transmembrane ion gradients. Such gradients are particularly useful for concentrating lipophilic cationic drugs inside liposomes, allowing trapping efficiencies approaching 100%. 相似文献
35.
36.
37.
Human blood was sheared between rotating polyethylene disks and plasma hemoglobin measured at intervals to produce kinetic
hemolysis curves (KHC), plotted as free hemoglobin concentration vs time. The KHC produced by blood samples incubated in the
presence of penicillin, streptomycin, gentamicin, and amikacin lie always below those for control samples, indicating a reduction
in hemolysis; this reduction was greater as the drug concentration was increased. Explanations in terms of alterations in
red cell structure were sought by several characterization tests of amikacin-loaded blood samples. Drug-localization studies
demonstrated that significant fractions of the total dosage were associated with the red-cell membrane. Resistive pulse spectroscopy
was used to show how amikacin affected cell size, deformability, and osmotic fragility; results were sensitive to storage
age of the blood. In all cases, the effect of shearing was to reduce cell size, deformability, and osmotic fragility. Mechanisms
for hemolytic protection by drugs are proposed. 相似文献
38.
Kawalek J. C., Rew R. S. and Heavner J. 1984. Glutathione-S-transferase, a possible drug-metabolizing enzyme in Haemonchus contortus: comparative activity of a cambendazole-resistant and a susceptible strain. International Journal for Parasitology14: 173–175. A drug metabolizing enzyme (DME), glutathione-S-transferase, was detected in homogenates of a cambendazole-susceptible and a cambendazole-resistant strain of Haemonchus contortus. The activity was 1.5–1.8 times higher in the resistant strain. DME activation is a possible mechanism for anthelmintic resistance in H. contortus. 相似文献
39.
40.
Esmail K. Shubber David Jacobson-Kram Dr. Jerry R. Williams 《Cell biology and toxicology》1986,2(3):379-399
Seven antischistosomal drugs, two antimalarial drugs, and one antiamoebic drug were tested in all five Ames strains for induction of mutation, as well as for induction of cytotoxicity, inhibition of cellular progression, and the induction of sister chromatid exchanges in two cultured mammalian cell lines. We found that two agents shown to be negative in the Ames test were positive for sister chromatid exchange induction. Based on qualitative and quantitative evaluation, we find that all but three of the pharmaceuticals should be considered to be potential human carcinogens.Abbreviations AA
2-aminoanthracene
- 9AACC
9-aminoacridine
- AM
amoscanate
- BrdUU
bromodeoxyuridine
- CA
chloroquine diphosphate
- CHO
Chinese hamster ovary
- CQ
chloroquine
- DAPI
46-diamidino-2-phenylindole
- DHY
dehydroemetine
- DMSO
dimethyl sulfoxide
- EB
ethidium bromide
- FCS
fetal calf serum
- FN
4-fluoro-3-nitrophenyl azide
- HY
hycanthone
- ICP
inhibiting cell progression
- LU
lucanthone
- MEM
minimal essential medium
- 2NF
2-nitrofurantoin
- 4NPD
4-nitro-O-phenylenediamine
- NZ
niridazole
- OL
oltipraz
- OX
oxaminiquine
- PBS
phosphate buffered saline
- PQ
primaquine
- PZ
praziquantel
- SA
sodium azide
- SCE
sister chromatid exchange 相似文献