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Chaptal, V.

Publications and source records attributed to Chaptal, V..

2 recordsLinked to original sources

CryoEM of ATP-driven dynamics and itraconazole binding in a fungal ABC pump

Azole resistance in Candida species is often caused by the overexpression of Cdr1. Despite its clinical relevance, the structural basis for its ATP-driven efflux pump function remains elusive. We present four high-resolution cryo-EM structures for Candida glabrata Cdr1 under active turnover conditions in the absence and presence of ATP-Mg{superscript 2}, itraconazole, and vanadate. Additional transient cryo-EM structures were unveiled by 3D variability analysis offering a detailed view of the step-by-step transitions triggered by ATP-hydrolysis. The motion cascade starts with a 4 [A] piston-like retraction of the C-helix from the {gamma}-phosphate/vanadate of the hydrolyzed ATP. This causes the nearby transmembrane helix-1 (TMH-1) to open the drug-binding site via lateral displacement and unwinding of the inner-leaflet region of TMH-2. A reverse squeeze-and-push motion of TMH-2 possibly drives substrate extrusion. High resolution structures also reveal how itraconazole adapts its shape to fit into the drug-binding site. Our findings provide a dynamic structural framework for Cdr1-mediated azole resistance and the conserved chemo-mechanical cycle of ABC proteins, including non-membranous members.

biochemistry↗

X-Ray Structure and enzymatic study of a Bacterial NADPHoxidase highlight the activation mechanism of eukaryoticNOX

NADPH oxidases (NOX) are transmembrane proteins that professionally produce reactive oxygen species (ROS) and are distributed widely in both eukaryotes and prokaryotes. Eukaryotes use the ROS products for innate immune defense and signaling; the seven human isoforms of NOX participate in critical physiological and pathophysiological processes. Recently solved structures of two human NOX isoforms provide much new information, but do not fully elucidate controls on the electron transfer pathway from NAD(P)H substrate through FAD and heme cofactors to the final ROS product. SpNOX, a bacterial NOX homolog from Streptococcus pneumoniae, shows robust constitutive activity in detergent solution, making it a good prototype for exploring electron transfer in the NOX family. Here we present crystal structures of wildtype and mutant full-length and dehydrogenase (DH) domain-only constructs of SpNOX. The isolated DH domain acts as a flavin reductase, and both DH and full-length constructs use either NADPH or NADH as substrate. Our data supports hydride transfer from NAD(P)H to FAD as the rate limiting step in electron transfer. Using the DH domain, we demonstrate the role of F397 in allowing access of nicotinamide to the flavin isoalloxazine, while in the full-length construct, we used mutants and flavin analogs to confirm the contribution of both domains to flavin binding observed in the structure. Comparison with homologous enzymes suggests distal heme access may influence the final electron acceptor, while the relative position of DH and TM does not necessarily correlate with activity of a given NOX family member. Based on this comparison, SpNOX appears to be a good model of active NOX2, which allows us to propose an explanation for NOX2s requirement for activation.

biochemistry↗