Search Results - "Pilch, D S"
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A Structural Model for the Ternary Cleavable Complex Formed between Human Topoisomerase I, DNA, and Camptothecin
Published in Biochemistry (Easton) (21-08-2001)“…Using the X-ray crystal structure of the human topoisomerase I (TOP1)−DNA cleavable complex, we have developed a general model for the ternary drug−DNA−TOP1…”
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Influence of Cisplatin Intrastrand Crosslinking on the Conformation, Thermal Stability, and Energetics of a 20-mer DNA Duplex
Published in Proceedings of the National Academy of Sciences - PNAS (23-07-1996)“…cis-Diamminedichloroplatinum(II) (cisplatin) is a widely used anticancer drug that binds to and crosslinks DNA. The major DNA adduct of the drug results from…”
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3
Binding of a Hairpin Polyamide in the Minor Groove of DNA: Sequence-Specific Enthalpic Discrimination
Published in Proceedings of the National Academy of Sciences - PNAS (06-08-1996)“…Hairpin polyamides are synthetic ligands for sequence-specific recognition in the minor groove of double-helical DNA. A thermodynamic characterization of the…”
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Structural analysis of the (dA)10.2(dT)10 triple helix
Published in Proceedings of the National Academy of Sciences - PNAS (01-03-1990)“…The existence of DNA triple helices in vitro has been known for some time. Recent evidence suggesting that DNA triplexes exist in vivo and showing their…”
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5
Heterocyclic bibenzimidazole derivatives as topoisomerase I inhibitors
Published in Bioorganic & medicinal chemistry letters (17-04-2000)“…A series of 2'-heterocyclic derivatives of 5-phenyl-2,5'-1H-bibenzimidazoles were evaluated for topoisomerase I poisoning activity and cytotoxicity. Topo I…”
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Structure, stability, and thermodynamics of a short intermolecular purine-purine-pyrimidine triple helix
Published in Biochemistry (Easton) (25-06-1991)“…We have investigated the structure and physical chemistry of the d(C3T4C3).2[d(G3A4G3)] triple helix by polyacrylamide gel electrophoresis (PAGE), 1H NMR, and…”
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Thermodynamics of triple helix formation : spectrophotometric studies on the d(A)10.2d(T)10 and d(C+3T4C+3)•d(G3A4G3)•d(C3T4C3) triple helices
Published in Nucleic acids research (11-10-1990)“…We have stabilized the d(A)10.2d(T)10 and d(C+LT4C+3).d(G3A4G3).d(C3T4C3) triple helices with either NaCl or MgCl2 at pH 5.5. UV mixing curves demonstrate a…”
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8
Ligand-Induced Formation of Nucleic Acid Triple Helices
Published in Proceedings of the National Academy of Sciences - PNAS (27-09-1994)“…We demonstrate that ligand binding can be used to induce the formation of triplex structures that would not otherwise form. Specifically, we show that binding…”
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Thermodynamics of Aminoglycoside−rRNA Recognition: The Binding of Neomycin-Class Aminoglycosides to the A Site of 16S rRNA
Published in Biochemistry (Easton) (18-06-2002)“…We use spectroscopic and calorimetric techniques to characterize the binding of the aminoglycoside antibiotics neomycin, paromomycin, and ribostamycin to a RNA…”
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Site-Specific Topoisomerase I-Mediated DNA Cleavage Induced by Nogalamycin: A Potential Role of Ligand-Induced DNA Bending at a Distal Site
Published in Biochemistry (Easton) (15-08-2000)“…Many DNA binding ligands (e.g., nogalamycin, actinomycin D, terbenzimidazoles, indolocarbazoles, nitidine, and coralyne) and various types of DNA lesions…”
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Defining the Basis for the Specificity of Aminoglycoside-rRNA Recognition: A Comparative Study of Drug Binding to the A Sites of Escherichia coli and Human rRNA
Published in Journal of molecular biology (11-02-2005)“…2-Deoxystreptamine (2-DOS) aminoglycoside antibiotics exert their antimicrobial activities by targeting the decoding region A site of the rRNA and inhibiting…”
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12
2-substituted 5-phenylterbenzimidazoles as topoisomerase I poisons
Published in Bioorganic & medicinal chemistry (01-06-2000)“…5-Phenylterbenzimidazole (1) is active as a topoisomerase I poison (topo I) and is cytotoxic to human tumor cells. No cross-resistance was observed for 1 when…”
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Thermodynamics of aminoglycoside-rRNA recognition
Published in Biopolymers (01-09-2003)“…2‐Deoxystreptamine (2‐DOS) aminoglycosides are a family of structurally related broad‐spectrum antibiotics that are used widely in the treatment of infections…”
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Human Topoisomerase I Poisoning by Protoberberines: Potential Roles for Both Drug−DNA and Drug−Enzyme Interactions
Published in Biochemistry (Easton) (20-06-2000)“…Protoberberines represent a structural class of organic cations that induce topoisomerase I-mediated DNA cleavage, a behavior termed topoisomerase I poisoning…”
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15
Aminoglycoside binding in the major groove of duplex RNA: the thermodynamic and electrostatic forces that govern recognition
Published in Journal of molecular biology (21-04-2000)“…We use a combination of spectroscopic, calorimetric, viscometric and computer modeling techniques to characterize the binding of the aminoglycoside antibiotic,…”
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Pentamidine inhibits catalytic activity of group I intron Ca.LSU by altering RNA folding
Published in Nucleic acids research (01-07-2002)“…The antimicrobial agent pentamidine inhibits the self-splicing of the group I intron Ca.LSU from the transcripts of the 26S rRNA gene of Candida albicans, but…”
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Deciphering the Origins of Observed Heat Capacity Changes for Aminoglycoside Binding to Prokaryotic and Eukaryotic Ribosomal RNA A-Sites: A Calorimetric, Computational, and Osmotic Stress Study
Published in Journal of the American Chemical Society (10-11-2004)“…Isothermal titration calorimetry (ITC), computational, and osmotic stress techniques have been used to characterize the changes in heat capacity,…”
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Berenil [1,3-bis(4'-amidinophenyl)triazene] binding to DNA duplexes and to a RNA duplex: evidence for both intercalative and minor groove binding properties
Published in Biochemistry (Easton) (08-08-1995)“…Berenil is an antitrypanosomal agent that binds to nucleic acid duplexes. The generally accepted mode of berenil binding is via complexation into the minor…”
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Minor Groove-Directed and Intercalative Ligand−DNA Interactions in the Poisoning of Human DNA Topoisomerase I by Protoberberine Analogs
Published in Biochemistry (Easton) (14-10-1997)“…Spectroscopic, calorimetric, DNA cleavage, electrophoretic, and computer modeling techniques have been employed to characterize the DNA binding and…”
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DNA sequence context modulates the impact of a cisplatin 1,2-d(GpG) intrastrand cross-link on the conformational and thermodynamic properties of duplex DNA
Published in Journal of molecular biology (25-02-2000)“…The anticancer activity of cisplatin derives from its ability to bind and cross-link DNA, with the major adduct being the 1,2-d(GpG) intrastrand cross-link…”
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