Structure-based virtual screening for fragment-like ligands of the G protein-coupled histamine H4 receptor

Research output: Contribution to journal › Journal article › Research › peer-review

Standard

Structure-based virtual screening for fragment-like ligands of the G protein-coupled histamine H4 receptor. / Istyastono, Enade P.; Istyastono, Enade P.; Kooistra, Albert J.; Vischer, Henry F.; Kuijer, Martien; Roumen, Luc; Nijmeijer, Saskia; Smits, Rogier A.; De Esch, Iwan J.P.; Leurs, Rob; De Graaf, Chris.

In: MedChemComm, Vol. 6, No. 6, 01.06.2015, p. 1003-1017.

Research output: Contribution to journal › Journal article › Research › peer-review

Harvard

Istyastono, EP, Istyastono, EP, Kooistra, AJ, Vischer, HF, Kuijer, M, Roumen, L, Nijmeijer, S, Smits, RA, De Esch, IJP, Leurs, R & De Graaf, C 2015, 'Structure-based virtual screening for fragment-like ligands of the G protein-coupled histamine H4 receptor', MedChemComm, vol. 6, no. 6, pp. 1003-1017. https://doi.org/10.1039/c5md00022j

APA

Istyastono, E. P., Istyastono, E. P., Kooistra, A. J., Vischer, H. F., Kuijer, M., Roumen, L., Nijmeijer, S., Smits, R. A., De Esch, I. J. P., Leurs, R., & De Graaf, C. (2015). Structure-based virtual screening for fragment-like ligands of the G protein-coupled histamine H4 receptor. MedChemComm, 6(6), 1003-1017. https://doi.org/10.1039/c5md00022j

Vancouver

Istyastono EP, Istyastono EP, Kooistra AJ, Vischer HF, Kuijer M, Roumen L et al. Structure-based virtual screening for fragment-like ligands of the G protein-coupled histamine H4 receptor. MedChemComm. 2015 Jun 1;6(6):1003-1017. https://doi.org/10.1039/c5md00022j

Author

Istyastono, Enade P. ; Istyastono, Enade P. ; Kooistra, Albert J. ; Vischer, Henry F. ; Kuijer, Martien ; Roumen, Luc ; Nijmeijer, Saskia ; Smits, Rogier A. ; De Esch, Iwan J.P. ; Leurs, Rob ; De Graaf, Chris. / Structure-based virtual screening for fragment-like ligands of the G protein-coupled histamine H4 receptor. In: MedChemComm. 2015 ; Vol. 6, No. 6. pp. 1003-1017.

Bibtex

@article{8f1000b2140f48adb421873de0227999,
title = "Structure-based virtual screening for fragment-like ligands of the G protein-coupled histamine H4 receptor",
abstract = "We have explored the possibilities and challenges of structure-based virtual screening (SBVS) against the human histamine H4 receptor (H4R), a key player in inflammatory responses. Several SBVS strategies, employing different H4R ligand conformations, were validated and optimized with respect to their ability to discriminate small fragment-like H4R ligands from true inactive fragments, and compared to ligand-based virtual screening (LBVS) approaches. SBVS studies with a molecular interaction fingerprint (IFP) scoring method enabled the identification of H4R ligands that were not identified in LBVS runs, demonstrating the scaffold hopping potential of combining molecular docking and IFP scoring. Retrospective VS evaluations against H4R homology models based on the histamine H1 receptor (H1R) crystal structure did not give higher enrichments of H4R ligands than H4R models based on the beta-2 adrenergic receptor (β2R). Complementary prospective SBVS studies against β2R-based and H1R-based H4R homology models led to the discovery of different new fragment-like H4R ligand chemotypes. Of the 37 tested compounds, 9 fragments (representing 5 different scaffolds) had affinities between 0.14 and 6.3 μM at the H4R.",
author = "Istyastono, {Enade P.} and Istyastono, {Enade P.} and Kooistra, {Albert J.} and Vischer, {Henry F.} and Martien Kuijer and Luc Roumen and Saskia Nijmeijer and Smits, {Rogier A.} and {De Esch}, {Iwan J.P.} and Rob Leurs and {De Graaf}, Chris",
year = "2015",
month = jun,
day = "1",
doi = "10.1039/c5md00022j",
language = "English",
volume = "6",
pages = "1003--1017",
journal = "MedChemComm",
issn = "2040-2503",
publisher = "Royal Society of Chemistry",
number = "6",

}

RIS

TY - JOUR

T1 - Structure-based virtual screening for fragment-like ligands of the G protein-coupled histamine H4 receptor

AU - Istyastono, Enade P.

AU - Istyastono, Enade P.

AU - Kooistra, Albert J.

AU - Vischer, Henry F.

AU - Kuijer, Martien

AU - Roumen, Luc

AU - Nijmeijer, Saskia

AU - Smits, Rogier A.

AU - De Esch, Iwan J.P.

AU - Leurs, Rob

AU - De Graaf, Chris

PY - 2015/6/1

Y1 - 2015/6/1

N2 - We have explored the possibilities and challenges of structure-based virtual screening (SBVS) against the human histamine H4 receptor (H4R), a key player in inflammatory responses. Several SBVS strategies, employing different H4R ligand conformations, were validated and optimized with respect to their ability to discriminate small fragment-like H4R ligands from true inactive fragments, and compared to ligand-based virtual screening (LBVS) approaches. SBVS studies with a molecular interaction fingerprint (IFP) scoring method enabled the identification of H4R ligands that were not identified in LBVS runs, demonstrating the scaffold hopping potential of combining molecular docking and IFP scoring. Retrospective VS evaluations against H4R homology models based on the histamine H1 receptor (H1R) crystal structure did not give higher enrichments of H4R ligands than H4R models based on the beta-2 adrenergic receptor (β2R). Complementary prospective SBVS studies against β2R-based and H1R-based H4R homology models led to the discovery of different new fragment-like H4R ligand chemotypes. Of the 37 tested compounds, 9 fragments (representing 5 different scaffolds) had affinities between 0.14 and 6.3 μM at the H4R.

AB - We have explored the possibilities and challenges of structure-based virtual screening (SBVS) against the human histamine H4 receptor (H4R), a key player in inflammatory responses. Several SBVS strategies, employing different H4R ligand conformations, were validated and optimized with respect to their ability to discriminate small fragment-like H4R ligands from true inactive fragments, and compared to ligand-based virtual screening (LBVS) approaches. SBVS studies with a molecular interaction fingerprint (IFP) scoring method enabled the identification of H4R ligands that were not identified in LBVS runs, demonstrating the scaffold hopping potential of combining molecular docking and IFP scoring. Retrospective VS evaluations against H4R homology models based on the histamine H1 receptor (H1R) crystal structure did not give higher enrichments of H4R ligands than H4R models based on the beta-2 adrenergic receptor (β2R). Complementary prospective SBVS studies against β2R-based and H1R-based H4R homology models led to the discovery of different new fragment-like H4R ligand chemotypes. Of the 37 tested compounds, 9 fragments (representing 5 different scaffolds) had affinities between 0.14 and 6.3 μM at the H4R.

UR - http://www.scopus.com/inward/record.url?scp=84930228441&partnerID=8YFLogxK

U2 - 10.1039/c5md00022j

DO - 10.1039/c5md00022j

M3 - Journal article

VL - 6

SP - 1003

EP - 1017

JO - MedChemComm

JF - MedChemComm

SN - 2040-2503

IS - 6

ER -

ID: 199353166