Helix Bundle Loops Determine Whether Histidine Kinases Autophosphorylate in cis or in trans

TitleHelix Bundle Loops Determine Whether Histidine Kinases Autophosphorylate in cis or in trans
Publication TypeJournal Article
Year of Publication2013
AuthorsAshenberg O, Keating AE, Laub MT
JournalJournal of Molecular Biology
Volume425
Pagination1198–1209
ISSN00222836
KeywordsAmino Acid, Amino Acid Sequence, Bacterial Outer Membrane Proteins, Bacterial Outer Membrane Proteins: chemistry, Bacterial Outer Membrane Proteins: genetics, Bacterial Outer Membrane Proteins: metabolism, Bacterial Proteins, Bacterial Proteins: chemistry, Bacterial Proteins: genetics, Bacterial Proteins: metabolism, Electrophoresis, Escherichia coli, Escherichia coli Proteins, Escherichia coli Proteins: chemistry, Escherichia coli Proteins: genetics, Escherichia coli Proteins: metabolism, Escherichia coli: genetics, Escherichia coli: metabolism, Fluorescence Resonance Energy Transfer, Kinetics, Luminescent Proteins, Luminescent Proteins: genetics, Luminescent Proteins: metabolism, Models, Molecular, Molecular Sequence Data, Multienzyme Complexes, Multienzyme Complexes: chemistry, Multienzyme Complexes: genetics, Multienzyme Complexes: metabolism, Mutation, Phosphorylation, Polyacrylamide Gel, Protein Conformation, Protein Kinases, Protein Kinases: chemistry, Protein Kinases: genetics, Protein Kinases: metabolism, Protein Multimerization, Protein Structure, Secondary, Sequence Homology, Tertiary
Abstract

Bacteria frequently use two-component signal transduction pathways to sense and respond to environmental and intracellular stimuli. Upon receipt of a stimulus, a homodimeric sensor histidine kinase autophosphorylates and then transfers its phosphoryl group to a cognate response regulator. The autophosphorylation of histidine kinases has been reported to occur both in cis and in trans, but the molecular determinants dictating which mechanism is employed are unknown. Based on structural considerations, one model posits that the handedness of a loop at the base of the helical dimerization domain plays a critical role. Here, we tested this model by replacing the loop from Escherichia coli EnvZ, which autophosphorylates in trans, with the loop from three PhoR orthologs that autophosphorylate in cis. These chimeric kinases autophosphorylated in cis, indicating that this small loop is sufficient to determine autophosphorylation mechanism. Further, we report that the mechanism of autophosphorylation is conserved in orthologous sets of histidine kinases despite highly dissimilar loop sequences. These findings suggest that histidine kinases are under selective pressure to maintain their mode of autophosphorylation, but they can do so with a wide range of sequences.

URLhttp://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=3636764&tool=pmcentrez&rendertype=abstract
DOI10.1016/j.jmb.2013.01.011