Literature DB >> 19167254

Molecular modeling of the heterodimer of human CFTR's nucleotide-binding domains using a protein-protein docking approach.

Sheng-You Huang1, Diana Bolser, Hao-Yang Liu, Tzyh-Chang Hwang, Xiaoqin Zou.   

Abstract

We have presented a new protein-protein docking approach to model heterodimeric structures based on the conformations of the monomeric units. The conventional modeling method relies on superimposing two monomeric structures onto the crystal structure of a homologous protein dimer. The resulting structure may exhibit severe backbone clashes at the dimeric interface depending on the backbone dissimilarity between the target and template proteins. Our method overcomes the backbone clashing problem and requires no a priori knowledge of the dimeric structure of a homologous protein. Here we used human Cystic Fibrosis Transmembrane conductance Regulator (CFTR), a chloride channel whose dysfunction causes cystic fibrosis, for illustration. The two intracellular nucleotide-binding domains (NBDs) of CFTR control the opening and closing of the channel. Yet, the structure of the CFTR's NBD1-NBD2 complex has not been experimentally determined. Thus, correct modeling of this heterodimeric structure is valuable for understanding CFTR functions and would have potential applications for drug design for cystic fibrosis treatment. Based on the crystal structure of human CFTR's NBD1, we constructed a model of the NBD1-NBD2 complex. The constructed model is consistent with the dimeric mode observed in the crystal structures of other ABC transporters. To verify our structural model, an ATP substrate was docked into the nucleotide-binding site. The predicted binding mode shows consistency with related crystallographic findings and CFTR functional studies. Finally, genistein, an agent that enhances CFTR activity, though the mechanism for such enhancement is unclear, was docked to the model. Our predictions agreed with genistein's bell-shaped dose-response relationship. Potential mutagenesis experiments were proposed for understanding the potentiation mechanism of genistein and for providing insightful information for drug design targeting at CFTR. The method used in this study can be applied to modeling studies of other dimeric protein structures.

Entities:  

Mesh:

Substances:

Year:  2008        PMID: 19167254      PMCID: PMC2758335          DOI: 10.1016/j.jmgm.2008.12.005

Source DB:  PubMed          Journal:  J Mol Graph Model        ISSN: 1093-3263            Impact factor:   2.518


  48 in total

1.  DOCK 4.0: search strategies for automated molecular docking of flexible molecule databases.

Authors:  T J Ewing; S Makino; A G Skillman; I D Kuntz
Journal:  J Comput Aided Mol Des       Date:  2001-05       Impact factor: 3.686

Review 2.  ATP hydrolysis-coupled gating of CFTR chloride channels: structure and function.

Authors:  X Zou; T C Hwang
Journal:  Biochemistry       Date:  2001-05-15       Impact factor: 3.162

3.  A novel shape complementarity scoring function for protein-protein docking.

Authors:  Rong Chen; Zhiping Weng
Journal:  Proteins       Date:  2003-05-15

4.  An iterative knowledge-based scoring function for protein-protein recognition.

Authors:  Sheng-You Huang; Xiaoqin Zou
Journal:  Proteins       Date:  2008-08

Review 5.  Molecular pharmacology of the CFTR Cl- channel.

Authors:  T C Hwang; D N Sheppard
Journal:  Trends Pharmacol Sci       Date:  1999-11       Impact factor: 14.819

6.  A common mechanism for cystic fibrosis transmembrane conductance regulator protein activation by genistein and benzimidazolone analogs.

Authors:  L Al-Nakkash; S Hu; M Li; T C Hwang
Journal:  J Pharmacol Exp Ther       Date:  2001-02       Impact factor: 4.030

7.  The E. coli BtuCD structure: a framework for ABC transporter architecture and mechanism.

Authors:  Kaspar P Locher; Allen T Lee; Douglas C Rees
Journal:  Science       Date:  2002-05-10       Impact factor: 47.728

8.  The First Nucleotide Binding Domain of Cystic Fibrosis Transmembrane Conductance Regulator Is a Site of Stable Nucleotide Interaction, whereas the Second Is a Site of Rapid Turnover.

Authors:  Luba Aleksandrov; Andrei A Aleksandrov; Xiu-Bao Chang; John R Riordan
Journal:  J Biol Chem       Date:  2002-02-22       Impact factor: 5.157

9.  The cystic fibrosis mutation G551D alters the non-Michaelis-Menten behavior of the cystic fibrosis transmembrane conductance regulator (CFTR) channel and abolishes the inhibitory Genistein binding site.

Authors:  Renaud Derand; Laurence Bulteau-Pignoux; Frédéric Becq
Journal:  J Biol Chem       Date:  2002-07-17       Impact factor: 5.157

10.  ATP binding to the motor domain from an ABC transporter drives formation of a nucleotide sandwich dimer.

Authors:  Paul C Smith; Nathan Karpowich; Linda Millen; Jonathan E Moody; Jane Rosen; Philip J Thomas; John F Hunt
Journal:  Mol Cell       Date:  2002-07       Impact factor: 17.970

View more
  12 in total

1.  Small molecule correctors of F508del-CFTR discovered by structure-based virtual screening.

Authors:  Ori Kalid; Martin Mense; Sharon Fischman; Alina Shitrit; Hermann Bihler; Efrat Ben-Zeev; Nili Schutz; Nicoletta Pedemonte; Philip J Thomas; Robert J Bridges; Diana R Wetmore; Yael Marantz; Hanoch Senderowitz
Journal:  J Comput Aided Mol Des       Date:  2010-10-26       Impact factor: 3.686

2.  Modulation of cystic fibrosis transmembrane conductance regulator (CFTR) activity and genistein binding by cytosolic pH.

Authors:  Raffaella Melani; Valeria Tomati; Luis J V Galietta; Olga Zegarra-Moran
Journal:  J Biol Chem       Date:  2010-10-25       Impact factor: 5.157

3.  Pseudohalide anions reveal a novel extracellular site for potentiators to increase CFTR function.

Authors:  Man-Song Li; Elizabeth A Cowley; Paul Linsdell
Journal:  Br J Pharmacol       Date:  2012-11       Impact factor: 8.739

4.  Potentiation of disease-associated cystic fibrosis transmembrane conductance regulator mutants by hydrolyzable ATP analogs.

Authors:  Haruna Miki; Zhen Zhou; Min Li; Tzyh-Chang Hwang; Silvia G Bompadre
Journal:  J Biol Chem       Date:  2010-04-20       Impact factor: 5.157

5.  Introduction to section IV: biophysical methods to approach CFTR structure.

Authors:  Juan L Mendoza; André Schmidt; Philip J Thomas
Journal:  Methods Mol Biol       Date:  2011

Review 6.  Molecular modelling and molecular dynamics of CFTR.

Authors:  Isabelle Callebaut; Brice Hoffmann; Pierre Lehn; Jean-Paul Mornon
Journal:  Cell Mol Life Sci       Date:  2016-10-07       Impact factor: 9.261

Review 7.  Dynamics intrinsic to cystic fibrosis transmembrane conductance regulator function and stability.

Authors:  P Andrew Chong; Pradeep Kota; Nikolay V Dokholyan; Julie D Forman-Kay
Journal:  Cold Spring Harb Perspect Med       Date:  2013-03-01       Impact factor: 6.915

Review 8.  Curcumin and genistein: the combined effects on disease-associated CFTR mutants and their clinical implications.

Authors:  Yoshiro Sohma; Ying-Chun Yu; Tzyh-Chang Hwang
Journal:  Curr Pharm Des       Date:  2013       Impact factor: 3.116

Review 9.  Structural mechanisms of CFTR function and dysfunction.

Authors:  Tzyh-Chang Hwang; Jiunn-Tyng Yeh; Jingyao Zhang; Ying-Chun Yu; Han-I Yeh; Samantha Destefano
Journal:  J Gen Physiol       Date:  2018-03-26       Impact factor: 4.086

Review 10.  Gating of the CFTR Cl- channel by ATP-driven nucleotide-binding domain dimerisation.

Authors:  Tzyh-Chang Hwang; David N Sheppard
Journal:  J Physiol       Date:  2009-03-30       Impact factor: 5.182

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.