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Des Georges, A.

Publications and source records attributed to Des Georges, A..

3 recordsLinked to original sources

Structural basis of the lobster carapace blue colour mediated by an HPR protein

The chemical basis underlying the striking blue hue of live H. americanus, known as American lobster, are studied in evolutionary biology and in polyene physical chemistry. Carapace colouration is generated by the antioxidant astaxanthin bound within the carotenoprotein crustacyanin complexes. Here, we present the ex vivo structure of the most abundant -crustacyanin and {beta}-crustacyanin forms, determined respectively by cryo-electron microscopy and X-ray crystallography to a resolution of 2.75 [A]. Our structural analysis reveals -crustacyanin as an elongated arrangement of {beta}-crustacyanin heterodimers tethered by an heptatricopeptide repeat (HPR) protein. In vitro complex formation between the {beta}-crustacyanin unit with a synthetic heptatricopeptide reproduces the observed blue colour of -crustacyanin, identifying the HPR protein, in concert with crustacyanins, as contributor in tuning carapace colour. Overall, these results explain how nature adjusts the colour across the entire visible spectrum by exploiting the bathochromic shift of astaxanthin from its unbound red form ({lambda}max = 472 nm) firstly to the {beta}-crustacyanin violet bound form ({lambda}max = 591 nm), and then to the -crustacyanin bound blue form ({lambda}max = 631 nm).

biochemistry↗

Structural identification of the RY12 domain of RyR1 as an ADP sensor and the target of the malignant hyperthermia therapeutic dantrolene

Malignant hyperthermia (MH) is a life-threatening pharmacogenetic condition triggered by volatile anesthetics, which activate pathogenic RyR1 mutants. The small molecule therapeutic dantrolene has long been used to treat MH. However, the binding site and mechanism of dantrolene remain unclear. Here, we present cryo-EM structures of RyR1 bound to dantrolene and the MH trigger agent 4-chloro-m-cresol (4CmC), revealing the dantrolene and 4CmC binding sites in atomic detail. Dantrolene binds stacked with ATP or ADP in the RY12 domain at the corner of the receptor, inducing a conformational change in this domain which is allosterically coupled to pore closure. Functional analyses revealed that ATP or ADP was required for dantrolene inhibition, and a single point mutation that disrupts the peripheral ATP binding site abolished ATP/ADP-dependent dantrolene inhibition. Strikingly, in the absence of dantrolene, this site selectively binds two ADP molecules, suggesting a possible role in ATP/ADP ratio sensing.

biophysics↗

ENRICH: a fast method to improve the quality of flexible macromolecular reconstructions

Cryo-electron microscopy using single particle analysis requires the computational averaging of thousands of projection images captured from identical macromolecules. However, macromolecules usually present some degree of flexibility showing different conformations. Computational approaches are then required to classify heterogeneous single particle images into homogeneous sets corresponding to different structural states. Nonetheless, sometimes the attainable resolution of reconstructions obtained from these smaller homogeneous sets is compromised because of reduced number of particles or lack of images at certain macromolecular orientations. In these situations, the current solution to improve map resolution is returning to the electron microscope and collect more data. In this work, we present a fast approach to partially overcome this limitation for heterogeneous data sets. Our method is based on deforming and then moving particles between different conformations using an optical flow approach. Particles are then merged into a unique conformation obtaining reconstructions with improved resolution, contrast and signal-to-noise ratio, then, partially circumventing many issues that impact obtaining high quality reconstructions from small data sets. We present experimental results that show clear improvements in the quality of obtained 3D maps, however, there are also limits to this approach, which we discuss in the manuscript.

bioengineering↗