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- WITTUNG, P, et al.
(författare)
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PHOSPHOLIPID MEMBRANE-PERMEABILITY OF PEPTIDE NUCLEIC-ACID
- 1995
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Ingår i: FEBS LETTERS. - 0014-5793. ; 365:1, s. 27-29
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Tidskriftsartikel (refereegranskat)abstract
- Phospholipid vesicles (liposomes) as membrane models have been used to study the penetration properties of peptide nucleic acid (PNA), a new DNA analog in which the nucleobases are attached to a pseudo-peptide backbone, The liposomes were characterised by
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| 2. |
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| 3. |
- López-Puertas, M., et al.
(författare)
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Non-local thermodynamic equilibrium limb radiances for the mipas instrument on Envisat-1
- 1998
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Ingår i: Journal of Quantitative Spectroscopy and Radiative Transfer. - 0022-4073 .- 1879-1352. ; 59:3-5, s. 377-403
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Tidskriftsartikel (refereegranskat)abstract
- An evaluation of the effects that the assumption of local thermodynamic equilibrium (LTE) has on the retrieval of pressure, temperature and the five primary target gases (O3, H2O, CH4, N2O, and HNO3) from spectra to be taken by Michelson Interferometer for Passive Atmospheric Sounding (MIPAS) on the Envisat-1 platform has been conducted. For doing so, non-LTE and LTE limb radiances in the spectral range of 680–2275 cm−1 (4.15–14.6 μm) with a resolution of 0.05 cm−1 at tangent heights from 10 to 70 km have been computed. These calculations included the most updated non-LTE populations of a large number of vibrational levels of the CO2, O3, H2O, CH4, N2O and HNO3 molecules which cause the most prominent atmospheric infrared emissions. A discussion of the most important non-LTE effects on the limb radiances as well as on the retrievals of pressure-temperature and volume mixing ratios of O3, H2O, CH4, N2O, and HNO3 is presented, together with the most important non-LTE issues that could be studied with the future coming of MIPAS data.
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| 4. |
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| 5. |
- Newman, D J, et al.
(författare)
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Serum cystatin C measured by automated immunoassay : a more sensitive marker of changes in GFR than serum creatinine
- 1995
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Ingår i: Kidney International. - : Elsevier BV. - 0085-2538. ; 47, s. 312-318
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Tidskriftsartikel (refereegranskat)abstract
- Serum cystatin C has been suggested as a new marker of GFR. For the introduction of this marker into clinical use a rapid and automated method is required. We have developed and validated an assay for serum cystatin C using latex particle-enhanced immunoturbidimetry. Intra- and inter-assay precision were < 3% and < 5% across the assay range. Analytical recovery was 93 +/- 3.8% and no lack of parallelism was demonstrated. Regression analysis of a method comparison with an enzyme-enhanced radial-immunodiffusion method, gave PETIA = 0.074 + 0.93 x SRID, r = 0.98, N = 100. Inter-assay precision profiles showed cystatin C was measured with two-fold better precision than creatinine on the same analyzer. Cystatin C measurement was neither interfered with by icterus nor by hemolysis. 1/cystatin C versus 1/creatinine concentrations gave r = 0.67, N = 469. Comparison of Cr EDTA GFR with 1/cystatin C and 1/creatinine gave r = 0.81 and 0.50, respectively, N = 206. Calculating diagnostic sensitivity for abnormal GFR showed cystatin C to be significantly (P < 0.05) more sensitive than creatinine (71.4 vs. 52.4%). Cystatin C measurement using PETIA technology can be automated on the same instruments used routinely for the measurement of creatinine and offers better analytical performance and probably improved clinical sensitivity as a screening test for early renal damage.
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| 9. |
- Wasan, E K, et al.
(författare)
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A multi-step lipid mixing assay to model structural changes in cationic lipoplexes used for in vitro transfection
- 1999
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Ingår i: Biochimica et Biophysica Acta - Biomembranes. - 0005-2736 .- 1879-2642. ; 1461:1, s. 27-46
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Tidskriftsartikel (refereegranskat)abstract
- Formation of liposome/polynucleotide complexes (lipoplexes) involves electrostatic interactions, which induce changes in liposome structure. The ability of these complexes to transfer DNA into cells is dependent on the physicochemical attributes of the complexes, therefore characterization of binding-induced changes in liposomes is critical for the development of lipid-based DNA delivery systems. To clarify the apparent lack of correlation between membrane fusion and in vitro transfection previously observed, we performed a multi-step lipid mixing assay to model the sequential steps involved in transfection. The roles of anion charge density, charge ratio and presence of salt on lipid mixing and liposome aggregation were investigated. The resonance-energy transfer method was used to monitor lipid mixing as cationic liposomes (DODAC/DOPE and DODAC/DOPC; 1:1 mole ratio) were combined with plasmid, oligonucleotides or Na(2)HPO(4). Cryo-transmission electron microscopy was performed to assess morphology. As plasmid or oligonucleotide concentration increased, lipid mixing and aggregation increased, but with Na(2)HPO(4) only aggregation occurred. NaCl (150 mM) reduced the extent of lipid mixing. Transfection studies suggest that the presence of salt during complexation had minimal effects on in vitro transfection. These data give new information about the effects of polynucleotide binding to cationic liposomes, illustrating the complicated nature of anion induced changes in liposome morphology and membrane behavior.
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| 10. |
- Wittung, Pernilla, 1968, et al.
(författare)
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Phospholipid membrane permeability of peptide nucleic acid
- 1995
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Ingår i: FEBS Letters. - : Wiley. - 1873-3468 .- 0014-5793. ; 365:1, s. 27-29
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Tidskriftsartikel (refereegranskat)abstract
- Phospholipid vesicles (liposomes) as membrane models have been used to study the penetration properties of peptide nucleic acid (PNA), a new DNA analog in which the nucleobases are attached to a pseudo-peptide backbone, The liposomes were characterised by carboxyfluorescein efflux, light-scattering and cryogenic transmission electron microscopy. The liposome structure was found not to be affected by the incorporation of PNA or an oligonucleotide. Two 10-mer fluorescein-labelled PNAs were found to have low efflux rates (half-times of 5.5 and 11 days), comparable to a 10-mer oligonucleotide (half-time of 7 days). We conclude that passive diffusion of unmodified PNA is not an effective way of transport into biological cells.
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