Kinetics of interaction of HIV reverse transcriptase with primer/template. 1993

G Divita, and B Müller, and U Immendörfer, and M Gautel, and K Rittinger, and T Restle, and R S Goody
Abteilung Biophysik, Max-Planck-Institut für Medizinische Forschung, Heidelberg, Germany.

Intrinsic protein fluorescence of reverse transcriptases from HIV-1 and HIV-2 provides a sensitive signal for monitoring the interaction of the enzymes with primer/template duplex molecules. Kd values for 18/36-mer DNA/DNA duplexes were found to be in the range of a few nanomolar (about 3 times higher for the enzyme from HIV-2 than for that from HIV-1). The quenching of protein fluorescence induced on binding primer/template, together with an increase in extrinsic fluorescence on interaction with primer/template containing a fluorescent nucleotide at the 3'-end of the primer, was used to investigate the kinetics of interaction with reverse transcriptase from HIV-1. The results can be explained in terms of a two-step binding model, with a rapid diffusion-limited initial association (k(ass) = ca. 5 x 10(8) M-1 s-1) followed by a slow isomerization step (k = ca. 0.5 s-1). These (forward) rate constants are increased in the presence of a non-nucleoside inhibitor (S-TIBO) of HIV-1 reverse transcriptase, while the reverse rate constant for the second step is decreased, leading to an increase in affinity between the enzyme and primer/template by a factor of at least 10 when S-TIBO is bound. The results are discussed in terms of present knowledge of the structure of reverse transcriptase.

UI MeSH Term Description Entries
D007093 Imidazoles Compounds containing 1,3-diazole, a five membered aromatic ring containing two nitrogen atoms separated by one of the carbons. Chemically reduced ones include IMIDAZOLINES and IMIDAZOLIDINES. Distinguish from 1,2-diazole (PYRAZOLES).
D007700 Kinetics The rate dynamics in chemical or physical systems.
D008956 Models, Chemical Theoretical representations that simulate the behavior or activity of chemical processes or phenomena; includes the use of mathematical equations, computers, and other electronic equipment. Chemical Models,Chemical Model,Model, Chemical
D008969 Molecular Sequence Data Descriptions of specific amino acid, carbohydrate, or nucleotide sequences which have appeared in the published literature and/or are deposited in and maintained by databanks such as GENBANK, European Molecular Biology Laboratory (EMBL), National Biomedical Research Foundation (NBRF), or other sequence repositories. Sequence Data, Molecular,Molecular Sequencing Data,Data, Molecular Sequence,Data, Molecular Sequencing,Sequencing Data, Molecular
D011485 Protein Binding The process in which substances, either endogenous or exogenous, bind to proteins, peptides, enzymes, protein precursors, or allied compounds. Specific protein-binding measures are often used as assays in diagnostic assessments. Plasma Protein Binding Capacity,Binding, Protein
D011994 Recombinant Proteins Proteins prepared by recombinant DNA technology. Biosynthetic Protein,Biosynthetic Proteins,DNA Recombinant Proteins,Recombinant Protein,Proteins, Biosynthetic,Proteins, Recombinant DNA,DNA Proteins, Recombinant,Protein, Biosynthetic,Protein, Recombinant,Proteins, DNA Recombinant,Proteins, Recombinant,Recombinant DNA Proteins,Recombinant Proteins, DNA
D004277 DNA, Single-Stranded A single chain of deoxyribonucleotides that occurs in some bacteria and viruses. It usually exists as a covalently closed circle. Single-Stranded DNA,DNA, Single Stranded,Single Stranded DNA
D001483 Base Sequence The sequence of PURINES and PYRIMIDINES in nucleic acids and polynucleotides. It is also called nucleotide sequence. DNA Sequence,Nucleotide Sequence,RNA Sequence,DNA Sequences,Base Sequences,Nucleotide Sequences,RNA Sequences,Sequence, Base,Sequence, DNA,Sequence, Nucleotide,Sequence, RNA,Sequences, Base,Sequences, DNA,Sequences, Nucleotide,Sequences, RNA
D001569 Benzodiazepines A group of two-ring heterocyclic compounds consisting of a benzene ring fused to a diazepine ring. Benzodiazepine,Benzodiazepine Compounds
D012194 RNA-Directed DNA Polymerase An enzyme that synthesizes DNA on an RNA template. It is encoded by the pol gene of retroviruses and by certain retrovirus-like elements. EC 2.7.7.49. DNA Polymerase, RNA-Directed,RNA-Dependent DNA Polymerase,Reverse Transcriptase,RNA Transcriptase,Revertase,DNA Polymerase, RNA Directed,DNA Polymerase, RNA-Dependent,RNA Dependent DNA Polymerase,RNA Directed DNA Polymerase

Related Publications

G Divita, and B Müller, and U Immendörfer, and M Gautel, and K Rittinger, and T Restle, and R S Goody
January 1998, Progress in nucleic acid research and molecular biology,
G Divita, and B Müller, and U Immendörfer, and M Gautel, and K Rittinger, and T Restle, and R S Goody
August 2005, The Journal of biological chemistry,
G Divita, and B Müller, and U Immendörfer, and M Gautel, and K Rittinger, and T Restle, and R S Goody
October 1997, Proceedings of the National Academy of Sciences of the United States of America,
G Divita, and B Müller, and U Immendörfer, and M Gautel, and K Rittinger, and T Restle, and R S Goody
April 1991, The Journal of biological chemistry,
G Divita, and B Müller, and U Immendörfer, and M Gautel, and K Rittinger, and T Restle, and R S Goody
June 1994, Journal of molecular recognition : JMR,
G Divita, and B Müller, and U Immendörfer, and M Gautel, and K Rittinger, and T Restle, and R S Goody
January 2008, PloS one,
G Divita, and B Müller, and U Immendörfer, and M Gautel, and K Rittinger, and T Restle, and R S Goody
October 1994, The Journal of biological chemistry,
G Divita, and B Müller, and U Immendörfer, and M Gautel, and K Rittinger, and T Restle, and R S Goody
July 1991, The Journal of biological chemistry,
G Divita, and B Müller, and U Immendörfer, and M Gautel, and K Rittinger, and T Restle, and R S Goody
July 1996, Biochemistry,
G Divita, and B Müller, and U Immendörfer, and M Gautel, and K Rittinger, and T Restle, and R S Goody
October 2007, Journal of molecular biology,
Copied contents to your clipboard!