Bacterial production and refolding from inclusion bodies of a “Weak” toxin, a disulfide rich protein

[1]  D. Bertrand,et al.  Naturally Occurring Disulfide-bound Dimers of Three-fingered Toxins , 2008, Journal of Biological Chemistry.

[2]  D. Bertrand,et al.  Bacterial Expression, NMR, and Electrophysiology Analysis of Chimeric Short/Long-chain α-Neurotoxins Acting on Neuronal Nicotinic Receptors* , 2007, Journal of Biological Chemistry.

[3]  D. A. Kuzmin,et al.  Computer modeling of binding of diverse weak toxins to nicotinic acetylcholine receptors , 2007, Comput. Biol. Chem..

[4]  N. Unwin,et al.  Refined structure of the nicotinic acetylcholine receptor at 4A resolution. , 2005, Journal of molecular biology.

[5]  F. Hucho,et al.  Snake and snail toxins acting on nicotinic acetylcholine receptors: fundamental aspects and medical applications , 2004, FEBS letters.

[6]  J. Changeux,et al.  Functional nicotinic acetylcholine receptors are expressed in B lymphocyte-derived cell lines. , 2003, Molecular pharmacology.

[7]  A. Arseniev,et al.  Resonance assignment of13C−15N-labeled snake neurotoxin II fromNaja oxiana , 2003 .

[8]  P. Gopalakrishnakone,et al.  Non-conventional toxins from Elapid venoms. , 2003, Toxicon : official journal of the International Society on Toxinology.

[9]  V. Klyushnichenko,et al.  Recombinant human insulin IX. Investigation of factors, influencing the folding of fusion protein-S-sulfonates, biotechnological precursors of human insulin. , 2002, Protein expression and purification.

[10]  Arunmozhiarasi Armugam,et al.  A synthetic weak neurotoxin binds with low affinity to Torpedo and chicken alpha7 nicotinic acetylcholine receptors. , 2002, European journal of biochemistry.

[11]  Yongbao Wang,et al.  A unique approach for high level expression and production of a recombinant cobra neurotoxin in Escherichia coli. , 2002, Journal of biotechnology.

[12]  A. Eletsky,et al.  First tryptophan-containing weak neurotoxin from cobra venom. , 2001, Toxicon : official journal of the International Society on Toxinology.

[13]  D Bertrand,et al.  “Weak Toxin” from Naja kaouthia Is a Nontoxic Antagonist of α7 and Muscle-type Nicotinic Acetylcholine Receptors* , 2001, The Journal of Biological Chemistry.

[14]  V. Klyushnichenko,et al.  Recombinant human insulin. VIII. Isolation of fusion protein--S-sulfonate, biotechnological precursor of human insulin, from the biomass of transformed Escherichia coli cells. , 2001, Protein expression and purification.

[15]  D. Bertrand,et al.  Neuronal nicotinic acetylcholine receptors: from the gene to the disease , 2000, Behavioural Brain Research.

[16]  P. Selvin,et al.  A comparison between the sulfhydryl reductants tris(2-carboxyethyl)phosphine and dithiothreitol for use in protein biochemistry. , 1999, Analytical biochemistry.

[17]  D Bertrand,et al.  Only Snake Curaremimetic Toxins with a Fifth Disulfide Bond Have High Affinity for the Neuronal α7 Nicotinic Receptor* , 1997, The Journal of Biological Chemistry.

[18]  S. Zinn-Justin,et al.  High-level production and isotope labeling of snake neurotoxins, disulfide-rich proteins. , 1997, Protein expression and purification.

[19]  D. I. Rzhevsky,et al.  Weak neurotoxin from Naja kaouthia cobra venom affects haemodynamic regulation by acting on acetylcholine receptors. , 2005, Toxicon : official journal of the International Society on Toxinology.

[20]  D. Bertrand,et al.  Nicotinic acetylcholine receptors: from structure to brain function. , 2003, Reviews of physiology, biochemistry and pharmacology.