Literature DB >> 7727450

NMR and restrained molecular dynamics study of the three-dimensional solution structure of toxin FS2, a specific blocker of the L-type calcium channel, isolated from black mamba venom.

J P Albrand1, M J Blackledge, F Pascaud, M Hollecker, D Marion.   

Abstract

The three-dimensional solution structure of toxin FS2, a 60-residue polypeptide isolated from the venom of black mamba snake (Dendroaspis polylepis polylepis), has been determined by nuclear magnetic resonance spectroscopy. Using 600 NOE constraints and 55 dihedral angle constraints, a set of 20 structures obtained from distance-geometry calculations was further refined by molecular dynamics calculations using a combined simulated annealing-restrained MD protocol. The resulting 20 conformers, taken to represent the solution structure, give an average rmsd of 1.2 A for their backbone atoms, relative to the average structure. The overall resulting three-fingered structure is similar to those already observed in several postsynaptic neurotoxins, cardiotoxins, and fasciculins, which all share with toxin FS2 the same network of four disulfide bridges. The overall concavity of the molecule, considered as a flat bottomed dish, is oriented toward the C-terminal loop of the molecule. This orientation is similar to that of fasciculins and cardiotoxins but opposite to that of neurotoxins. On the basis of the local rms displacements between the 20 conformers, the structure of the first loop appears to be less well defined in FS2 than in the previously reported neurotoxin structures, but fasciculin 1 shows a similar trend with particularly high temperature factors for this part of the X-ray structure. The concave side which presents most of the positively charged residues is quite similar in FS2 and fasciculin 1. The main difference is shown by the convex side of the third loop, mostly hydrophobic in FS2, in contrast to the pair of negatively charged aspartates in fasciculin 1. This difference could be one of the factors leading to the distinct pharmacological properties-L-type calcium channel blocker for FS2 and cholinesterase inhibitor for fasciculin--observed for these two subgroups of the "angusticeps-type" toxins.

Entities:  

Mesh:

Substances:

Year:  1995        PMID: 7727450     DOI: 10.1021/bi00017a022

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  16 in total

1.  NMR structure of bucandin, a neurotoxin from the venom of the Malayan krait (Bungarus candidus).

Authors:  A M Torres; R M Kini; N Selvanayagam; P W Kuchel
Journal:  Biochem J       Date:  2001-12-15       Impact factor: 3.857

2.  Cytotoxic potency of cardiotoxin from Naja sputatrix: development of a new cytolytic assay.

Authors:  Donghui Ma; Arunmozhiarasi Armugam; Kandiah Jeyaseelan
Journal:  Biochem J       Date:  2002-08-15       Impact factor: 3.857

Review 3.  Diversity of folds in animal toxins acting on ion channels.

Authors:  Stéphanie Mouhat; Besma Jouirou; Amor Mosbah; Michel De Waard; Jean-Marc Sabatier
Journal:  Biochem J       Date:  2004-03-15       Impact factor: 3.857

Review 4.  Anticoagulant proteins from snake venoms: structure, function and mechanism.

Authors:  R Manjunatha Kini
Journal:  Biochem J       Date:  2006-08-01       Impact factor: 3.857

Review 5.  Privileged frameworks from snake venom.

Authors:  T A Reeks; B G Fry; P F Alewood
Journal:  Cell Mol Life Sci       Date:  2015-02-19       Impact factor: 9.261

6.  Differential induction of interleukin-10 in monocytes by HIV-1 clade B and clade C Tat proteins.

Authors:  Justine K Wong; Grant R Campbell; Stephen A Spector
Journal:  J Biol Chem       Date:  2010-04-08       Impact factor: 5.157

7.  Comparative molecular modelling study of the calcium channel blockers nifedipine and black mamba toxin FS2.

Authors:  K J Schleifer
Journal:  J Comput Aided Mol Des       Date:  1997-09       Impact factor: 3.686

8.  Transcriptomic analysis of the venom gland of the red-headed krait (Bungarus flaviceps) using expressed sequence tags.

Authors:  Ang Swee Siang; Robin Doley; Freek J Vonk; R Manjunatha Kini
Journal:  BMC Mol Biol       Date:  2010-03-29       Impact factor: 2.946

9.  Role of accelerated segment switch in exons to alter targeting (ASSET) in the molecular evolution of snake venom proteins.

Authors:  Robin Doley; Stephen P Mackessy; R Manjunatha Kini
Journal:  BMC Evol Biol       Date:  2009-06-30       Impact factor: 3.260

10.  SLEEPLESS, a Ly-6/neurotoxin family member, regulates the levels, localization and activity of Shaker.

Authors:  Mark N Wu; William J Joiner; Terry Dean; Zhifeng Yue; Corinne J Smith; Dechun Chen; Toshinori Hoshi; Amita Sehgal; Kyunghee Koh
Journal:  Nat Neurosci       Date:  2009-12-13       Impact factor: 24.884

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.