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Structure and Function of the Transmembrane Domain of NsaS, an Antibiotic Sensing Histidine Kinase in Staphylococcus aureus
- Bhate, Manasi P., Lemmin, Thomas, Kuenze, Georg, Mensa, Bruk, Ganguly, Soumya, Peters, Jason M., Schmidt, Nathan, Pelton, Jeffrey G., Gross, Carol A., Meiler, Jens, DeGrado, William F.
- Journal of the American Chemical Society 2018 v.140 no.24 pp. 7471-7485
- Staphylococcus aureus, active sites, antibiotics, deformation, histidine kinase, humans, innate immunity, molecular models, nuclear magnetic resonance spectroscopy, pathogens, proteins
- NsaS is one of four intramembrane histidine kinases (HKs) in Staphylococcus aureus that mediate the pathogen’s response to membrane active antimicrobials and human innate immunity. We describe the first integrative structural study of NsaS using a combination of solution state NMR spectroscopy, chemical-cross-linking, molecular modeling and dynamics. Three key structural features emerge: First, NsaS has a short N-terminal amphiphilic helix that anchors its transmembrane (TM) bundle into the inner leaflet of the membrane such that it might sense neighboring proteins or membrane deformations. Second, the transmembrane domain of NsaS is a 4-helix bundle with significant dynamics and structural deformations at the membrane interface. Third, the intracellular linker connecting the TM domain to the cytoplasmic catalytic domains of NsaS is a marginally stable helical dimer, with one state likely to be a coiled-coil. Data from chemical shifts, heteronuclear NOE, H/D exchange measurements and molecular modeling suggest that this linker might adopt different conformations during antibiotic induced signaling.