| 1. |
- Brenning, Nils, et al.
(author)
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Critical ionization velocity interaction in the CRIT I rocket experiment
- 1990
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In: Advances in Space Research. - : Elsevier BV. - 0273-1177. ; 10, s. 63-66
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Journal article (peer-reviewed)abstract
- In the rocket experiment CRIT I, launched from Wallops Island on 13 May 1986, two identical Barium shaped charges were fired from distances of 1.3 km and 3.6 km towards the main experiment payload, which was separated from a sub-payload by a couple of km along the magnetic field. The relevance of earlier proposed mechanisms for electron heating in ionospheric critical velocity experiments is investigated in the light of the CRIT I results. It is concluded that both the "homogeneous" and the "ionizing front" models can be applied, in different parts of the stream. It is also possible that a third, entirely different, mechanism may contribute to the electron heating. This mechanism involves direct energization of electrons in the magnetic-field-aligned component of the DC electric field. © 1989.
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| 2. |
- Brenning, Nils, et al.
(author)
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Electrodynamic interaction between the CRIT I ionized barium streams and the ambient ionosphere
- 1990
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In: Advances in Space Research. - : Elsevier BV. - 0273-1177. ; 10, s. 67-70
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Journal article (peer-reviewed)abstract
- In the CRIT I Critical Velocity experiment, launched from Wallops Island on 13 May, 1986, two fast barium streams were ejected by means of shaped charges. Their electrodynamic interaction with the ambient ionosphere is discussed. An outstanding feature of the DC electric field observed within the streams was a large magnetic-field-aligned component, persisting on the time scale of the passage of the streams. One interpretation of the DC electric field data is that the internal electric fields of the streams is not greatly modified by Birkeland currents, i.e. a state is established, where the transverse currents are to a first approximation divergence-free. It is argued that this interpretation can explain why a reversal of the strong explosion-directed electric field was observed in the first explosion but not in the second (more distant one). © 1989.
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| 3. |
- Brenning, Nils, et al.
(author)
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Interpretation of the Electric Fields Measured in an Ionospheric Critical Ionization Velocity Experiment
- 1991
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In: Journal of Geophysical Research. - 0148-0227 .- 2156-2202. ; 96, s. 9719-9733
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Journal article (peer-reviewed)abstract
- This paper deals with the quasi-dc electric fields measured in the CRIT I ionospheric release experiment, which was launched from Wallops Island on May 13, 1986. The purpose of the experiment was to study the critical ionization velocity (CIV) mechanism in the ionosphere. Two identical barium shaped charges were fired from distances of 1.99 km and 4.34 km towards a main payload, which made full three-dimensional measurements of the electric field inside the streams. There was also a subpayload separated from the main payload by a couple of kilometers along the magnetic field. The relevance of earlier proposed mechanisms for electron heating in CIV is investigated in the light of the CRIT I results. It is concluded that both the “homogeneous” and the “ionizing front” models probably apply, but in different parts of the stream. It is also possible that electrons are directly accelerated by a magnetic-field-aligned component of the electric field; the quasi-dc electric field observed within the streams had a large magnetic-field-aligned component, persisting on the time scale of the passage of the streams. The coupling between the ambient ionosphere and the ionized barium stream in CRIT I was more complicated than is usually assumed in CIV theories, with strong magnetic-field-aligned electric fields and probably current limitation as important processes. One interpretation of the quasi-dc electric field data is that the internal electric fields of the streams were not greatly modified by magnetic-field-aligned currents, i.e., a state was established where the transverse currents were to a first approximation divergence-free. It is argued that this interpretation can explain both a reversal of the strong explosion-directed electric field in burst 1 and the absence of such a reversal in burst 2.
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| 4. |
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| 5. |
- Egholm, M., et al.
(author)
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PNA HYBRIDIZES TO COMPLEMENTARY OLIGONUCLEOTIDES OBEYING THE WATSON-CRICK HYDROGEN-BONDING RULES
- 1993
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In: Nature. - : Springer Science and Business Media LLC. - 0028-0836 .- 1476-4687. ; 365:6446, s. 566-568
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Journal article (peer-reviewed)abstract
- DNA ANALOGUES are currently being intensely investigated owing to their potential as gene-targeted drugs1-3. Furthermore, their properties and interaction with DNA and RNA could provide a better understanding of the structural features of natural DNA that determine its unique chemical, biological and genetic properties3,4. We recently designed a DNA analogue, PNA, in which the backbone is structurally homomorphous with the deoxyribose backbone and consists of N-(2-aminoethyl)glycine units to which the nucleobases are attached5-9. We showed that PNA oligomers containing solely thymine and cytosine can hybridize to complementary oligonucleotides, presumably by forming Watson-Crick-Hoogsteen (PNA)2-DNA triplexes, which are much more stable than the corresponding DNA-DNA duplexes5-7, and bind to double-stranded DNA by strand displacement5,8. We report here that PNA containing all four natural nucleobases hybridizes to complementary oligonucleotides obeying the Watson-Crick base-pairing rules, and thus is a true DNA mimic in terms of base-pair recognition.
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| 6. |
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| 7. |
- Holst, J., et al.
(author)
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Protamine neutralization of intravenous and subcutaneous low-molecular-weight heparin (tinzaparin, Logiparin(TM)). An experimental investigation in healthy volunteers
- 1994
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In: Blood Coagulation and Fibrinolysis. - 0957-5235. ; 5:5, s. 795-803
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Journal article (peer-reviewed)abstract
- The aim of the present study was to investigate whether tinzaparin sodium (a low-molecular-weight heparin (LMWH)) was fully and permanently neutralized in vivo in man by protamine sulphate (PS) after intravenous (i.v.) or subcutaneous (s.c.) injection. Fifty healthy adults equally divided in five age- and sex-matched groups were included. The groups received 50 IU unfractionated heparin (UH)/kg body weight (b.w.) i.v., 50 anti-factor Xa (anti-Xa) IU tinzaparin/kg b.w. i.v., 75 anti-Xa IU tinzaparin/kg b.w. s.c., 175 anti-Xa IU tinzaparin/kg b.w. s.c., or 1 ml of saline s.c. PS was given as a 10 min infusion in a dose of 1 mg/100 IU of heparin in the four first groups while 0.5 mg PS/kg b.w. was given in the placebo group. In the i.v. groups PS was administered 45 min after the heparin injection, and in the s.c. groups 180 min post-heparin injection. In the UH group PS fully and permanently neutralized all three activities. In the i.v. tinzaparin group PS reversed 80% of the anti-Xa activity, while the anti-IIa and aPTT activities were fully reversed. A slight, but statistically significant, increase in anti-Xa and anti-Ila activities were seen following i.v. tinzaparin. In the s.c. groups 60-65% of the observed peak anti-Xa activity was neutralized, anti-IIa was almost completely reversed, and aPTT returned nearly to baseline values. A gradual return of the anti-Xa activity (65-75%), anti-IIa activity (55%) and aPTT activity (35-45%) was seen in the s.c. groups 3 h after reversal compared with the observed peak values. A continuous absorption of tinzaparin from the s.c. depot is presumably the cause of the returned activity. PS caused an 8-27% transient drop in the platelet count in all groups. This study confirms that the anti-Xa activity following i.v. and s.c. administration of tinzaparin (a LMWH) is only partially neutralizable by protamine. This is not due to insufficient dosages of the antidote, as an excess of protamine could be demonstrated ex vivo immediately after the protamine infusion. The present results suggest that protamine neutralization of tinzaparin given s.c. should be obtained with intermittent injections or continuous infusion.
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| 8. |
- Kim, Seog K., et al.
(author)
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RIGHT-HANDED TRIPLEX FORMED BETWEEN PEPTIDE NUCLEIC-ACID PNA-T(8) AND POLY(DA) SHOWN BY LINEAR AND CIRCULAR-DICHROISM SPECTROSCOPY
- 1993
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In: Journal of the American Chemical Society. - : American Chemical Society (ACS). - 1520-5126 .- 0002-7863. ; 115:15, s. 6477-6481
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Journal article (peer-reviewed)abstract
- The binding of an eightmer of peptide nucleic acid, H-T8-Lys-NH2 (=PNA-T8), to a polynucleotide, poly(dA), was studied by flow linear dichroism (LD) and circular dichroism (CD) spectroscopy. Whereas the single stranded DNA, due to its high flexibility, does not display any measurable LD signal when subjected to shear flow, the complex with PNA does. A titration shows that saturation occurs at a stoichiometry of two PNA thymine bases per DNA adenine base, indicating the formation of a triplex PNA2-DNA complex. The persistence length of the adduct remains small up to relatively high stoichiometries (above 1:1 T:A) indicating that no significant amounts of PNA:DNA duplex are formed. Instead triplex stretches seem to form surrounded by flexible parts of single stranded poly(dA). Upon approaching the stoichiometry 2:1 of T:A the LD increases dramatically demonstrating that the stiffness of the PNA-DNA triplex arises from base-base contacts preventing bending of the chain. It is also inferred that the main stiffness of duplex DNA very probably has a similar origin and is not primarily a result of the increased phosphate-phosphate repulsion. Circular dichroism spectra support the conclusion that a triplex is formed as the only PNA-DNA complex and that it is a right-handed helix. The wavelength dependence of the reduced linear dichroism shows that the inclination of the bases from perpendicularity relative to the helix axis is small. The base conformation of the poly(dA)[PNA-T8]2 triplex is very similar to that of the conventional poly(dA)[poly(dT)]2 triplex.
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| 9. |
- Nielsen, P. E., et al.
(author)
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DNA-BINDING AND PHOTOCLEAVAGE BY URANYL(VI) (UO2(2+)) SALTS
- 1992
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In: Journal of the American Chemical Society. - : American Chemical Society (ACS). - 1520-5126 .- 0002-7863. ; 114:13, s. 4967-4975
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Journal article (peer-reviewed)abstract
- The interaction of the uranyl(VI) ion (UO22+) with DNA and its light-induced cleavage of DNA has been studied using flow-linear dichroism and P-32-endlabeled oligonucleotides. It was found that binding of uranyl ion to DNA is a prerequisite for photocleavage; from run-off experiments the binding constant was estimated to be of the order of 10(10) M-1 at pH 4. The angular orientation of the [O=U=O]2+ chromophore is consistent with binding by bridging phosphate groups on opposite strands of the minor groove of DNA; at higher DNA concentration aggregation indicates intermolecular bridging as well. The uranyl-mediated photocleavage of DNA is not influenced by the presence of O2, is more efficient at low pH (
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| 10. |
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