2004
Synthesis of isotopically labeled puromycin derivatives for kinetic isotope effect analysis of ribosome catalyzed peptide bond formation
Okuda K, Seila A, Strobel S. Synthesis of isotopically labeled puromycin derivatives for kinetic isotope effect analysis of ribosome catalyzed peptide bond formation. Tetrahedron 2004, 60: 12101-12112. DOI: 10.1016/j.tet.2004.10.023.Peer-Reviewed Original Research
1999
Nucleotide Analog Interference Mapping
Ryder S, Strobel S. Nucleotide Analog Interference Mapping. Methods 1999, 18: 38-50. PMID: 10208815, DOI: 10.1006/meth.1999.0755.Peer-Reviewed Original ResearchConceptsFunctional groupsActive moleculesGroup substitutionNucleotide analog interference mappingIncorporation propertiesIndividual analoguesMoleculesSeries 5AnaloguesSubstitution experimentsGel electrophoresisInterference mappingUnique biochemical signatureSubstitutionSynthesisNucleoside analog triphosphatesActivity assaysBiochemical informationReactionAnalog substitutionsAssayable functionChemogenetic approachRNA structureNucleotide analoguesIodineChemInform Abstract: The Synthesis of RNA Containing the Modified Nucleotides N2‐Methylguanosine and N6,N6‐Dimethyladenosine.
Rife J, Cheng C, Moore P, Strobel S. ChemInform Abstract: The Synthesis of RNA Containing the Modified Nucleotides N2‐Methylguanosine and N6,N6‐Dimethyladenosine. ChemInform 1999, 30: no-no. DOI: 10.1002/chin.199916227.Peer-Reviewed Original Research
1998
The Synthesis of RNA Containing the Modified Nucleotides N 2-Methylguanosine and N 6, N 6-Dimethyladenosine
Rife J, Cheng C, Moore P, Strobel S. The Synthesis of RNA Containing the Modified Nucleotides N 2-Methylguanosine and N 6, N 6-Dimethyladenosine. Nucleosides Nucleotides & Nucleic Acids 1998, 17: 2281-2288. DOI: 10.1080/07328319808004317.Peer-Reviewed Original Research