S. Gasparini

发表

High-level production and isotope labeling of snake neurotoxins, disulfide-rich proteins.

S. Zinn-Justin, A. Ménez, E. Lajeunesse, 1997, Protein expression and purification.

Effect of Rap1 binding on DNA distortion and potassium permanganate hypersensitivity.

E. Gilson, Y. Le Bihan, E. Le Cam, 2013, Acta crystallographica. Section D, Biological crystallography.

Three-dimensional structure of kappa-conotoxin PVIIA, a novel potassium channel-blocking toxin from cone snails.

S. Zinn-Justin, A. Ménez, B. Gilquin, 1998, Biochemistry.

On the site by which α‐dendrotoxin binds to voltage‐dependent potassium channels: Site‐directed mutagenesis reveals that the lysine triplet 28–30 is not essential for binding

A. Ménez, H. Vatanpour, E. Lajeunesse, 1994, FEBS letters.

Role of disulfide bonds in folding and activity of leiurotoxin I: just two disulfides suffice.

Loïc Martin, C. Vita, A. Ménez, 2002, Biochemistry.

The low molecular weight protein which co-purifies with alpha-latrotoxin is structurally related to crustacean hyperglycemic hormones.

E. Grishin, A. Ménez, P. Ripoche, 1994, The Journal of biological chemistry.

Mapping the Functional Anatomy of BgK on Kv1.1, Kv1.2, and Kv1.3

A. Ménez, A. Harvey, S. Gasparini, 1999, The Journal of Biological Chemistry.

Production of recombinant notechis 11'2L, an enzymatically active mutant of a phospholipase A2 from Notechis scutatus scutatus venom, as directly generated by cleavage of a fusion protein produced in Escherichia coli.

A. Ménez, F. Ducancel, J. Boulain, 1993, European journal of biochemistry.

The orientation of the C-terminal domain of the Saccharomyces cerevisiae Rap1 protein is determined by its binding to DNA

Y. Le Bihan, B. Castaing, S. Zinn-Justin, 2011, Nucleic acids research.

Structural analysis of the Smad2-MAN1 interaction that regulates transforming growth factor-β signaling at the inner nuclear membrane.

Wei Wu, S. Zinn-Justin, B. Gilquin, 2010, Biochemistry.

Subcellular localization of SREBP1 depends on its interaction with the C-terminal region of wild-type and disease related A-type lamins.

B. Buendia, P. Roussel, S. Zinn-Justin, 2011, Experimental cell research.

BgK, a disulfide-containing sea anemone toxin blocking K+ channels, can be produced in Escherichia coli cytoplasm as a functional tagged protein.

G. Mourier, A. Ménez, J. Boulain, 2004, Protein expression and purification.

Comparison of sea anemone and scorpion toxins binding to Kv1 channels: an example of convergent evolution.

A. Ménez, B. Gilquin, S. Gasparini, 2004, Toxicon : official journal of the International Society on Toxinology.

Identification of structurally and functionally important histidine residues in cytoplasmic aspartyl-tRNA synthetase from Saccharomyces cerevisiae.

G. Eriani, J. Gangloff, D. Kern, 1991, Biochemistry.

Structure of the BgK-Kv1.1 Complex Based on Distance Restraints Identified by Double Mutant Cycles

S. Grissmer, A. Ménez, B. Gilquin, 2002, The Journal of Biological Chemistry.

Delineation of the functional site of alpha-dendrotoxin. The functional topographies of dendrotoxins are different but share a conserved core with those of other Kv1 potassium channel-blocking toxins.

S. Zinn-Justin, A. Ménez, J. Danse, 1998, The Journal of biological chemistry.

A Variable Residue in the Pore of Kv1 Channels Is Critical for the High Affinity of Blockers from Sea Anemones and Scorpions*

B. Roux, M. Eriksson, A. Ménez, 2005, Journal of Biological Chemistry.

Delineation of the Functional Site of α-Dendrotoxin

S. Zinn-Justin, A. Ménez, J. Danse, 1998, Journal of Biological Chemistry.