Proceedings of the National Academy of Sciences · 1988 · 162 citations · 10 references
Saturation KineticsCross-coupling ReactionTransition State AnalogImmunocytochemical TechniqueBiochemistryClaisen RearrangementNatural SciencesImmunologyBioconjugationSynthetic BiologyAntibody ScreeningMonoclonal AntibodiesImmunochemistryAntibody EngineeringChemical BiologyMedicineAsymmetric Catalysis
Monoclonal antibodies were prepared against a transition state analog inhibitor of chorismate mutase (EC 5.4.99.5). One of the antibodies catalyzes the rearrangement of chorismate to prephenate with rate accelerations of more than 2 orders of magnitude compared to the uncatalyzed reaction. Saturation kinetics were observed, and at 25 degrees C the values of kcat and Km were 1.2 X 10(-3) s-1 and 5.1 X 10(-5) M respectively. The transition state analog was shown to be a competitive inhibitor of the reaction with Ki equal to 0.6 microM. These results demonstrate the feasibility of using rationally designed immunogens to generate antibodies that catalyze concerted reactions.
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Measurement of protein using bicinchoninic acid
Pam Smith, Randall I. Krohn, Greg T. Hermanson et al. · Analytical Biochemistry · 1985 · 18.2K citations
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