ABSTRACT
A GIS-based one-dimensional flood simulation model is presented and applied to the centre of the city of Nîmes (Gard, France), for mapping flow depths or velocities in the streets network. The geometry of the one-dimensional elements is derived from the Digital Elevation Model (DEM). The flow is routed from one element to the next using the kinematic wave approximation. At the crossroads, the flows in the downstream branches are computed using a conceptual scheme. This scheme was previously designed to fit Y-shaped pipes junctions, and has been modified here to fit X-shaped crossroads. The results were compared with the results of a two-dimensional hydrodynamic model based on the full shallow water equations. The comparison shows that good agreements can be found in the steepest streets of the study zone, but differences may be important in the other streets. Some reasons that can explain the differences between the two models are given and some research possibilities are proposed.
Subject(s)
Cities , Disasters , Models, Theoretical , Rain , Computer Simulation , Water MovementsABSTRACT
A new and efficient strategy for labeling of nucleic acids prior to their hybridization on high density DNA chip has been developed. Our approach which combines the fragmentation and the labeling is based on the reactivity of the terminal phosphates of cleaved DNA and RNA fragments with a reporter molecule bearing aryldiazomethane group.
Subject(s)
DNA/chemistry , Oligonucleotide Array Sequence Analysis/methods , RNA/chemistry , Hydrolysis , Indicators and Reagents , Molecular Conformation , Nucleic Acid HybridizationABSTRACT
The yield of hole injection into guanines of different oligonucleotide duplexes by a photooxidizing tethered Ru(II) complex is examined by measuring the luminescence quenching of the excited complex. This yield is investigated as a function of the anchoring site of the complex (on a thymine nucleobase in the middle of the sequence or on the 5' terminal phosphate) and the number and position of the guanine bases as compared with the site of attachment of the Ru(II) compound. In contrast to other studies, the tethered complex, [Ru(tap)(2)(dip)](2+), is a non-intercalating compound and has been shown previously to produce an irreversible photocrosslinking between the two strands as the ultimate step of hole injection. The study of luminescence quenching of the anchored complex by emission intensity and lifetime measurements for the different duplexes indicates that a direct contact between the complex and the guanine nucleobase is needed for the electron transfer to take place. Moreover, for none of the sequences a clear contribution of a static quenching is evidenced independently of the two types of attachment of the [Ru(tap)(2)(dip)](2+) complex to the oligonucleotide. A comparison of the fastest hole-injection process by electron transfer to the excited anchored [Ru(tap)(2)(dip)](2+), with the rate of the photo-electron transfer between the same complex free in solution and guanosine-5'-monophosphate, indicates that the hole injection by the anchored complex is slower by a factor of 10 at least. A bad overlap between donor and acceptor orbitals is probably the cause of this slow rate, which could be attributed to some steric hindrance induced by the complex linker.
Subject(s)
DNA/chemistry , Light , Ruthenium/chemistry , Binding Sites , DNA/metabolism , Electron Transport , Electrons , Guanine/chemistry , Kinetics , Models, Chemical , Models, Molecular , Nucleic Acid Conformation , Oligonucleotides/chemistry , Ultraviolet RaysABSTRACT
A convergent strategy for the synthesis of peptide-oligonucleotide conjugates (POC) is presented. Chemoselective ligation of peptide to oligonucleotide was accomplished by oxime and thiazolidine formation. Oxime conjugation was performed by treating an oxyamine-containing peptide with an aldehyde-containing oligonucleotide or vice versa. Ligation by thiazolidine formation was achieved by coupling a peptide, acylated with a cysteine residue, to an oligonucleotide that was derivatised by an aldehyde function. For both approaches, the conjugates were obtained in good yield without the need for a protection strategy and under mild aqueous conditions. Moreover, the oxime ligation proved useful for directly conjugating duplex oligonucleotides. Combined with molecular biology tools, this methodology opens up new prospects for post-functionalisation of high-molecular-weight DNA structures.
Subject(s)
Oligodeoxyribonucleotides/chemistry , Peptide Nucleic Acids/chemical synthesis , Peptides/chemistry , Amino Acid Sequence , Base Sequence , Oligodeoxyribonucleotides/chemical synthesis , Oligopeptides , Oximes , Peptides/chemical synthesis , ThiazolesABSTRACT
Three acridine-diaminopurine heterodimers tethered by a linker containing an N,N'-substituted guanidine were prepared. The molecules differ by the site of introduction of the linker on the 2,6-diaminopurine. The interactions of the new heterodimers with abasic site containing oligonucleotide were compared, and their cytotoxicity was measured in the presence or absence of the antitumor alkylating agent BCNU.
Subject(s)
2-Aminopurine/analogs & derivatives , 2-Aminopurine/metabolism , Acridines/metabolism , Intercalating Agents/metabolism , Oligonucleotides/metabolism , 2-Aminopurine/chemistry , 2-Aminopurine/pharmacology , Acridines/chemistry , Acridines/pharmacology , Animals , Base Sequence , Carmustine/pharmacology , Cell Line/cytology , Cell Line/drug effects , DNA Damage , Dimerization , Inhibitory Concentration 50 , Nucleic Acid Denaturation/radiation effects , Oligonucleotides/chemistry , Purines/chemistry , ThermodynamicsABSTRACT
A site-specifically modified oligonucleotide containing a single 2'-deoxyribonolactone lesion was used as a template for primer extension reactions catalyzed by M-MuLV reverse transcriptase (RT) and by the Klenow fragments of Escherichia coli DNA polymerase proficient (KF exo(+)) or deficient (KF exo(-)) in exonuclease activity. Analysis of the extension products in the presence of the four dNTPs or of a single dNTP showed that the M-MuLV RT was completely blocked and did not incorporate any dNMP opposite 2'-deoxyribonolactone. KF exo(-) preferentially incorporated nucleotides opposite the lesion following the frequency order dAMP > dGMP >> dTMP approximately dCMP and thus appeared to obey the 'A rule' for preferential incorporation as has been shown previously for the 2'-deoxyribose abasic site. In the sequence context examined, the primer extension by KF exo(-) appeared to be less efficient when dAMP was positioned opposite the lesion as compared with dTMP or dGMP. These two nucleotides promoted a more efficient polymerization accompanied by nucleotide deletion through misalignment incorporations. We therefore predict that the sequence context may strongly influence the translesional synthesis by KF exo(-) and thus the miscoding and mutational potential of the 2'-deoxyribonolactone in E.coli.
Subject(s)
DNA Damage/genetics , DNA Polymerase I/metabolism , DNA/biosynthesis , DNA/genetics , RNA-Directed DNA Polymerase/metabolism , Sugar Acids/metabolism , Base Sequence , Catalysis , DNA/chemistry , DNA/metabolism , Escherichia coli/enzymology , Exodeoxyribonucleases/metabolism , Kinetics , Moloney murine leukemia virus/enzymology , Mutagenesis/genetics , Nucleotides/metabolism , Oligonucleotides/chemical synthesis , Oligonucleotides/chemistry , Oligonucleotides/genetics , Oligonucleotides/metabolism , Templates, GeneticABSTRACT
We describe the synthesis, DNA binding measurements and pharmacological properties of a series of new heterodimeric molecules, in which a 2,6-diaminopurine is linked to a 9-aminoacridine chromophore. The linking chain contains a central N,N'-disubstituted guanidine, connected to the two chromophores by polymethylenic units of variable length.
Subject(s)
Antineoplastic Agents, Alkylating/pharmacology , Carmustine/pharmacology , DNA/drug effects , Adenocarcinoma/pathology , Animals , Cattle , Humans , Leukemia L1210/pathology , Lung Neoplasms/pathology , Magnetic Resonance Spectroscopy , Mice , Tumor Cells, CulturedABSTRACT
We describe the preparation of oligonucleotides containing a 5'-linker bearing an aminooxy group. Use of the trityl protecting group for the aminooxy moiety allows purification of the modified oligonucleotide by reverse phase HPLC and cleavage in mild acidic conditions. Derivatization with an aldehydic reporter group is efficient and rapid.
Subject(s)
Aldehydes/chemical synthesis , Oligodeoxyribonucleotides/chemical synthesis , Oligodeoxyribonucleotides/isolation & purification , Organophosphorus Compounds/chemical synthesis , Organophosphorus Compounds/isolation & purification , Chromatography, High Pressure Liquid , FluoresceinABSTRACT
We describe the reaction of oligonucleotides containing an aldehydic group at the 5'-end or inside the sequence with an oxyamino label. The reaction was found to be highly selective and represents an efficient method for derivatization of oligonucleotides.
Subject(s)
Aldehydes/chemistry , Fluorescent Dyes/chemistry , Oligodeoxyribonucleotides/chemical synthesis , Chromatography, High Pressure Liquid , DNA/chemistry , Molecular Structure , Oligodeoxyribonucleotides/chemistry , Spectrometry, Fluorescence , TemperatureABSTRACT
The DNA interaction of a chiral Tröger base derived from proflavine was investigated by DNA melting temperature measurements and complementary biochemical assays. DNase I footprinting experiments demonstrate that the binding of the proflavine-based Tröger base is both enantio- and sequence-specific. The (+)-isomer poorly interacts with DNA in a non-sequence-selective fashion. In sharp contrast, the corresponding (-)-isomer recognizes preferentially certain DNA sequences containing both A. T and G. C base pairs, such as the motifs 5'-GTT. AAC and 5'-ATGA. TCAT. This is the first experimental demonstration that acridine-type Tröger bases can be used for enantiospecific recognition of DNA sequences.
Subject(s)
DNA/metabolism , Proflavine/chemistry , Proflavine/metabolism , Animals , Base Pairing , Base Sequence , Binding Sites , Bridged-Ring Compounds/chemistry , Bridged-Ring Compounds/metabolism , Cattle , DNA/chemistry , DNA/genetics , DNA Footprinting , In Vitro Techniques , StereoisomerismABSTRACT
Abasic sites in DNA have been specifically targeted by synthetic compounds able to cleave DNA at abasic sites and to induce photodamages in the vicinity of the lesion. The synthesis and the photoactivity of the drugs on abasic sites containing DNA and oligonucleotides are reported.
Subject(s)
DNA Damage , DNA/drug effects , Antineoplastic Agents/pharmacology , DNA/chemistry , DNA/radiation effects , PhotochemistryABSTRACT
A new heterodimer adenine-chain-acridine containing a mixed amido-guanidinium linker chain was synthesized. To achieve the synthesis a new method of introduction of aminoalkyl chain at position 9 of adenine was designed. The heterodimer interacts specifically with the abasic sites in DNA and inhibits the major base excision repair enzyme in Escherichia coli, Exonuclease III.
Subject(s)
Acridines/chemistry , Adenine/chemistry , Enzyme Inhibitors/chemical synthesis , Enzyme Inhibitors/pharmacology , Exodeoxyribonucleases/antagonists & inhibitors , Animals , DNA/chemistry , DNA/drug effects , DNA Repair , Drug Screening Assays, Antitumor , Escherichia coli/enzymology , Humans , Mice , Tumor Cells, CulturedABSTRACT
On the basis of molecular modeling studies, the 7-nitroindole nucleoside 1 was selected as a suitable photochemical precursor for photochemical generation of the C1' deoxyribosyl radical under irradiation, which led to 2'-deoxyribonolactone. The nitro-indole nucleoside derivatives 1a and 1b were prepared and their conformation was determined by X-ray crystallography and NMR spectroscopy. The photoreaction of these nucleosides gave the corresponding deoxyribonolactone derivatives efficiently, with release of 7-nitrosoindole. This reaction was successfully applied to synthesis of oligonucleotides containing the deoxyribonolactone lesion.
ABSTRACT
Inhibition of abasic site repair in the cell seems an attractive strategy to potentiate the action of antitumor DNA alkylating drugs. Molecules that bind specifically and strongly to the abasic site are possible candidates to achieve such inhibition. We explored this strategy by preparing molecule 4 that incorporates (1) an aminoacridine intercalator for DNA binding, (2) an adenine moiety for abasic site recognition, and (3) a linker containing two guanidinium functions to increase binding to DNA without inducing cleavage at the base-sensitive abasic site. Compound 4 was compared to analogues containing secondary amines, i.e., 1. We report on synthesis of the new heterodimer 4. We show by physicochemical studies-including determination of association constants with calf-thymus DNA, T(m) measurements, and high-field NMR examination of the complexes formed with abasic DNA duplexes-that 4 binds specifically and more strongly to the abasic site than the analogues. Compound 4 does not cleave abasic plasmid DNA. Compound 4 shows apparent synergy with the anticancer bischloroethylnitrosourea (BCNU) in L1210 and A549 cell lines in vitro. It potentiates BCNU in the in vivo tests. The results favor the pertinence of the strategy.
Subject(s)
Antineoplastic Agents, Alkylating/metabolism , DNA, Neoplasm/metabolism , Animals , Antineoplastic Agents, Alkylating/chemistry , Antineoplastic Agents, Alkylating/pharmacology , Cattle , DNA, Neoplasm/chemistry , Drug Screening Assays, Antitumor , Female , Humans , Magnetic Resonance Spectroscopy , Mass Spectrometry , Mice , Mice, Inbred DBA , Molecular Structure , Nucleic Acid Denaturation , Tumor Cells, CulturedABSTRACT
The macrocyclic bisacridine (CBA) has been reported previously to specifically recognize single-stranded nucleic acid structures, especially DNA hairpins. The binding of the drug with an abasic site-containing oligonucleotide, was investigated by (1)H NMR and molecular modeling. We have used a DNA undecamer, the d(C(1)G(2)C(3)A(4)C(5)X(6)C(7)A(8)C(9)G(10)C(11)) x d(G(12)C(13)G(14)T(15)G(16)T(17)G(18)T(19)G(2)(0)C(21)G(22)) duplex in which the X residue is a stable analogue of the abasic site [3-hydroxy-2-(hydroxymethyl) tetrahydrofuran]. Analysis of the NMR data reveals that the bisacridine molecule forms two different intercalation complexes in a 80/20 (+/- 10) ratio. For the major complex, a molecular modeling study was performed guided by nineteen intermolecular drug-DNA restraints, determined from NOESY spectra. In this model, the ligand interacts in the threading binding mode with an acridine ring intercalated between the C(7)-A(8) and T(15)-G(16) base pairs, while the other acridine ring resides in the abasic pocket. The two linker chains are positioned in the minor and in the major groove, respectively. A comparable study was performed to evaluate the interaction of CBA with the parent unmodified duplex in which X(6) was replaced by an adenine residue. No complex formation was observed when operating in identical conditions. This shows the selective binding of CBA to the abasic site and its potential interest to target the abasic site lesion.
Subject(s)
Acridines/chemistry , DNA/chemistry , Intercalating Agents/chemistry , Models, Molecular , Oligonucleotides/chemistry , Acridines/metabolism , Binding Sites , DNA/metabolism , DNA Adducts/chemistry , DNA Adducts/metabolism , Furans/chemistry , Furans/metabolism , Intercalating Agents/metabolism , Kinetics , Nuclear Magnetic Resonance, Biomolecular , Nucleic Acid Conformation , Oligonucleotides/metabolism , ProtonsABSTRACT
The aim of the study was to analyze the impact of soci-economic status in addition to other risk factors in the progression of HIV disease in a cohort of injecting drug users (IDUs) with a mean follow-up of two years. Between 1989 and 1992, 124 HIV-infected IDUs were recruited in a primary care outpatient clinic providing free consultations and free access to therapy. The main outcome measures were death and AIDs-defining events. The proportion of current daily injectors at entry in the study and at the end of follow-up was 67.7% and 57.2%, respectively. The proportion of individuals on maintenance opioid therapy at entry in the study and at the end of follow-up was 0 and 12.1%, respectively. CD4 cell counts below 200 x 10(6)/L at baseline, positive p24 antigenemia at baseline, the lack of legal income and occasional drug use at entry were risk factors for clinical progression and death. When adjusted in a multivariate analysis, the absence of legal income remained associated with death and occurrence of an AIDS-defining event with a relative risk of 5.2 (1.5-18.1) (p = 0.004). Lack of legal income is a strong risk factor for progression of HIV disease in IDUs, that is independent of CD4 cell count and p24 antigenemia.
Subject(s)
HIV Infections/mortality , Substance Abuse, Intravenous/mortality , Acquired Immunodeficiency Syndrome/economics , Acquired Immunodeficiency Syndrome/etiology , Acquired Immunodeficiency Syndrome/mortality , Adult , Cohort Studies , Female , HIV Infections/complications , HIV Infections/economics , Humans , Income , Male , Multivariate Analysis , Paris/epidemiology , Risk Factors , Social Class , Socioeconomic Factors , Substance Abuse, Intravenous/complications , Substance Abuse, Intravenous/economicsABSTRACT
A novel method for the quantitation of abasic sites (AP sites) in DNA is described. As abasic sites can be generated by controlled thermal treatment of base-modified DNA, this method can be used for estimation of the extent of DNA damage resulting from exposure to genotoxic agents. The method involves use of probe molecules 1 and 2 that contain a fluorescent label linked to an aminooxy group which reacts specifically with the aldehydic function of the ring-opened form of abasic sites. The two fluorescent probes 1 and 2 were found to react with 2-deoxyribose, a model substrate, at the optimum of pH 4.0. As spontaneous depurination occurs at low pH, the reactions with abasic DNA were carried out at neutral pH with an excess concentration of the probes. Studies with alkylated, depurinated calf thymus DNA showed that the method is selective and quantitative. Good correlations were found between the level of 7-methylguanine (7-MeGua), generated in vitro in DNA by the methylating agent dimethyl sulfate, and the amount of AP sites as determined by the method presented here. In addition, similar correlations were found when the assay was used to detect abasic sites in DNA isolated from rats treated with carcinogenic alkylating agents. In each case, the level of abasic sites, as expected, is slightly higher than the level of 7-MeGua which is known to represent about 70% of the total modifications of DNA following exposure to the methylating agent. This method may be useful not only in experimental settings but also in studies of DNA damage in humans resulting from chemotherapy or exposure to environmental agents.
Subject(s)
DNA Damage , DNA/analysis , Animals , Cattle , Fluorescent Dyes , Guanine/analogs & derivatives , Guanine/metabolism , Hot Temperature , Hydrogen-Ion Concentration , Male , Rats , Sensitivity and SpecificityABSTRACT
The solution conformation of the DNA duplex d(C1G2C3A4C5L6C7A8C9G10C11).d(G12C13G14T15G16T17G18T19G20C21G22 ) containing the 2'-deoxyribonolactone lesion (L6) in the middle of the sequence has been investigated by NMR spectroscopy and restrained molecular dynamics calculations. Interproton distances have been obtained by complete relaxation matrix analysis of the NOESY cross-peak intensities. These distances, along with torsion angles for sugar rings and additional data derived from canonical A- and B-DNA, have been used for structure refinement by restrained molecular dynamics (rMD). Six rMD simulations have been carried out starting from both regular A- and B-DNA forms. The pairwise rms deviations calculated for each refined structure are <1 A, indicating convergence to essentially the same geometry. The accuracy of the rMD structures has been assessed by complete relaxation matrix back-calculation. The average sixth-root residual index (Rx = 0.052 +/- 0.003) indicated that a good fit between experimental and calculated NOESY spectra has been achieved. Detailed analysis revealed a right-handed DNA conformation for the duplex in which both the T17 nucleotide opposite the abasic site and the lactone ring are located inside the helix. No kinking is observed for this molecule, even at the abasic site step. This structure is compared to that of the oligonucleotide with the identical sequence containing the stable tetrahydrofuran abasic site analogue that we reported previously [Coppel, Y., Berthet, N., Coulombeau, C., Coulombeau, Ce., Garcia, J., and Lhomme, J. (1997) Biochemistry 36, 4817-4830].
Subject(s)
DNA Damage , DNA/chemistry , Models, Molecular , Sugar Acids/chemistry , Base Sequence , Glycosides/chemistry , Nuclear Magnetic Resonance, Biomolecular , Nucleic Acid Conformation , Nucleic Acid Heteroduplexes/chemistry , Oligodeoxyribonucleotides/chemistry , Phosphorus Isotopes , Protons , Ribonucleosides/chemistry , SolutionsABSTRACT
A series of molecules with apurinic/apyrimidic (AP) endonuclease activity targeted to abasic sites in DNA, which incorporate an intercalating moiety linked to a purine base by a polyamino chain and recognize and cleave abasic sites in DNA with high efficiency, has been studied. The aim was first to establish whether these compounds were inhibitors of base excision DNA repair, since abasic sites are generated during this process. Using an extension of a recently established methodology, two members of this series have been identified as definite repair inhibitors. Secondly, the potential of using such compounds as sensitizers of alkylating agents has been investigated by determining the cytotoxic activity of these compounds on L1210 cells in culture. A concentration-dependent potentiation of nitrosoureas has been demonstrated, but interpretation is complicated by the inherent cytotoxic properties of the test compounds themselves. Such molecules, however, provide interesting lead compounds for new strategies aimed at enhancing the cytotoxic potential of clinically useful DNA-damaging agents.