ABSTRACT
Triazolo[4,5-d]pyrimidin-5-amines were identified from kinase selectivity screening as novel ERK3 inhibitors with sub-100 nanomolar potencies in a biochemical assay using MK5 as substrate and with an attractive kinase selectivity profile. ERK3 crystal structures clarified the inhibitor binding mode in the ATP pocket with impact on A-loop, GC-loop and αC-helix conformations suggesting a potential structural link towards MK5 interaction via the FHIEDE motif. The inhibitors also showed sub-100 nM potencies in a cellular ERK3 NanoBRET assay and with excellent correlation to the biochemical IC50s. This novel series provides valuable tool compounds to further investigate the biological function and activation mechanism of ERK3.
Subject(s)
Mitogen-Activated Protein Kinase 6/antagonists & inhibitors , Protein Kinase Inhibitors/pharmacology , Crystallography, X-Ray , Dose-Response Relationship, Drug , Humans , Mitogen-Activated Protein Kinase 6/metabolism , Models, Molecular , Molecular Structure , Protein Kinase Inhibitors/chemical synthesis , Protein Kinase Inhibitors/chemistry , Structure-Activity RelationshipABSTRACT
Accurate ranking of compounds with regards to their binding affinity to a protein using computational methods is of great interest to pharmaceutical research. Physics-based free energy calculations are regarded as the most rigorous way to estimate binding affinity. In recent years, many retrospective studies carried out both in academia and industry have demonstrated its potential. Here, we present the results of large-scale prospective application of the FEP+ method in active drug discovery projects in an industry setting at Merck KGaA, Darmstadt, Germany. We compare these prospective data to results obtained on a new diverse, public benchmark of eight pharmaceutically relevant targets. Our results offer insights into the challenges faced when using free energy calculations in real-life drug discovery projects and identify limitations that could be tackled by future method development. The new public data set we provide to the community can support further method development and comparative benchmarking of free energy calculations.
Subject(s)
Drug Discovery , Ligands , Prospective Studies , Retrospective Studies , ThermodynamicsABSTRACT
RAF kinase plays a critical role in the RAF-MEK-ERK signaling pathway and inhibitors of RAF could be of use for the treatment of various cancer types. We have designed potent RAF-1 inhibitors bearing novel bicyclic heterocycles as key structural elements for the interaction with the hinge region. In both series exploration of the SAR was focussed on the substitution of the phenyl ring, which binds to the induced fit pocket. Overall, it was confirmed that incorporation of lipophilic substituents was needed for potent Raf inhibition and a number of potent analogues were obtained.
Subject(s)
Benzimidazoles/chemistry , Isoquinolines/chemistry , Protein Kinase Inhibitors/chemical synthesis , raf Kinases/antagonists & inhibitors , Benzimidazoles/chemical synthesis , Benzimidazoles/pharmacology , Binding Sites , Catalytic Domain , Computer Simulation , Drug Design , Isoquinolines/chemical synthesis , Isoquinolines/pharmacology , Protein Kinase Inhibitors/chemistry , Protein Kinase Inhibitors/pharmacology , Signal Transduction , Structure-Activity Relationship , raf Kinases/metabolismABSTRACT
In order to gain deeper insight into the function and interplay of proteins in cells it is essential to develop methods that allow the profiling of protein function in real time, in solution, in cells, and in cell organelles. Here we report the development of a U-type oligonucleotide (molecular beacon) that contains a fluorophore and a quencher at the tips, and in addition a substrate analogue in the loop structure. This substrate analogue induces a hairpin cleavage in response to enzyme action, which is translated into a fluorescence signal. The molecular beacon developed here was used to characterize DNA-photolyase activity. These enzymes represent a challenge for analytical methods because of their low abundance in cells. The molecular beacon made it possible to measure the activity of purified class I and class II photolyases. Photolyase activity was even detectable in crude cell extracts.
Subject(s)
Deoxyribodipyrimidine Photo-Lyase/metabolism , Molecular Probes/chemical synthesis , DNA Repair , Nucleic Acid Conformation , Oligonucleotides/chemical synthesisABSTRACT
The formamidopyrimidine (FapydGua) lesion, derived from the nucleobase guanine, is a major DNA lesion involved in mutagenesis and carcinogenesis. To date, the chemical information available about this main lesion is very limited. Herein, we describe a synthesis and a detailed characterization of the acetyl-protected monomer of the FapydGua lesion. Stability studies in DMSO and in water/acetonitrile show that the N-glycosidic bond, previously thought to be highly labile, is much more stable than anticipated. Decomposition of the FapydGua lesion proceeds with half-life times of 37.8 h for the beta-anomer and 65.2 h for the alpha-anomer in water/acetonitrile. The relaxation time for the anomerization reaction was determined to tau = 6.5 h at room temperature. Most important, it was found that the formamido group, which is critical for the lesion recognition process by repair enzymes, is fixed in the cis-conformation in apolar solvents such as chloroform. This conformation enables the formation of a hydrogen bond between the carbonyl oxygen of the formamide and the NH of the N-glycosidic bond within the framework of a seven-membered ring system. This has consequences for the recognition of the lesion by repair enzymes (hOGG1 and Fpg protein). These enzymes were so far believed to recognize the carbonyl group of the FapydGua lesion. Our investigations show that this carbonyl group is not readily accessible because it is almost buried in the dominating cis-conformation. In agreement with the recent X-ray structure of hOGG1 in complex with 8-oxo-7,8-dihydroguanine-containing DNA, we can conclude that repair enzymes can contact both lesions only via the N(7)-H group, which is a hydrogen-bond acceptor in guanine.
Subject(s)
DNA Damage , DNA Ligases/chemistry , DNA/chemistry , Guanine/analogs & derivatives , Guanine/chemistry , Pyrimidines/chemistry , Pyrimidines/chemical synthesis , Pyrimidinones/chemistry , 8-Hydroxy-2'-Deoxyguanosine/analogs & derivatives , Algorithms , Catalysis , Chromatography, High Pressure Liquid , Crystallography, X-Ray , DNA-Formamidopyrimidine Glycosylase , Dimethyl Sulfoxide , Guanine/chemical synthesis , Hydrogen Bonding , Imidazoles/chemical synthesis , Imidazoles/chemistry , Kinetics , Models, Molecular , Molecular Conformation , Molecular Structure , Mutagenesis , N-Glycosyl Hydrolases/chemistry , N-Glycosyl Hydrolases/metabolism , Nuclear Magnetic Resonance, Biomolecular , Oxazoles/chemical synthesis , Oxazoles/chemistry , RNA/chemistry , Spectrophotometry, Infrared , Stereoisomerism , Structure-Activity Relationship , Substrate Specificity , Time FactorsSubject(s)
DNA/chemistry , Electrons , Base Sequence , Biochemistry/methods , Chromatography, High Pressure Liquid , Electrochemistry/methods , Flavins/chemistry , Guanine/chemistry , Models, Chemical , Molecular Sequence Data , Nucleic Acid Conformation , Oligonucleotides/chemistry , Oxidative Stress , Spectrophotometry, Ultraviolet/methods , Thymine/chemistryABSTRACT
What is damaged cannot always be readily repaired. This is observed for particular areas in the genome (mutation hot spots), which are repaired with low efficiency. DNA-DNA duplexes that exist in the B-conformation are repaired relatively efficiently by photolyases. DNA-RNA duplexes, which prefer an A-type conformation are only moderately destabilized by DNA photolesions and are slowly repaired. This suggests that the DNA conformation modulates the necessary "flipping" process for the repair of DNA lesions.
