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Theoretical study of the binding profile of an allosteric modulator NS-1738 with a chimera structure of the alpha 7 nicotinic acetylcholine receptor

Guanglin, Kuang (author)
KTH,Teoretisk kemi och biologi,AlbaNova Univ Ctr, Sch Biotechnol, Royal Inst Technol KTH, Div Theoret Chem & Biol, S-10691 Stockholm, Sweden.
Wang, Xu (author)
KTH,Teoretisk kemi och biologi,AlbaNova Univ Ctr, Sch Biotechnol, Royal Inst Technol KTH, Div Theoret Chem & Biol, S-10691 Stockholm, Sweden.
Halldin, Christer (author)
Karolinska Institutet
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Nordberg, Agneta (author)
Karolinska Institutet
Långström, Bengt (author)
Uppsala universitet,Organisk kemi
Ågren, Hans (author)
KTH,Teoretisk kemi och biologi,AlbaNova Univ Ctr, Sch Biotechnol, Royal Inst Technol KTH, Div Theoret Chem & Biol, S-10691 Stockholm, Sweden.
Tu, Yaoquan (author)
KTH,Teoretisk kemi och biologi,AlbaNova Univ Ctr, Sch Biotechnol, Royal Inst Technol KTH, Div Theoret Chem & Biol, S-10691 Stockholm, Sweden.
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 (creator_code:org_t)
2016
2016
English.
In: Physical Chemistry, Chemical Physics - PCCP. - : Royal Society of Chemistry. - 1463-9076 .- 1463-9084. ; 18:40, s. 28003-28009
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Potentiation of the function of the alpha 7 nicotinic acetylcholine receptor (alpha 7-nAChR) is believed to provide a possible way for the treatment of cholinergic system dysfunctions such as Alzheimer's disease and schizophrenia. Positive allosteric modulators (PAMs) are able to augment the peak current response of the endogenous agonist of alpha 7-nAChR by binding to some allosteric sites. In this study, the binding profile of a potent type I PAM, NS-1738, with a chimera structure (termed alpha 7-AChBP) constructed from the extracellular domain of alpha 7-nAChR and an acetylcholine binding protein was investigated with molecular docking, molecular dynamics simulation, and free energy calculation methods. We found that NS-1738 could bind to three allosteric sites of alpha 7-AChBP, namely, the top pocket, the vestibule pocket and the agonist sub-pocket. NS-1738 has moderate binding affinities (-6.76 to -9.15 kcal mol(-1)) at each allosteric site. The urea group is critical for binding and can form hydrogen-bond interactions with the protein. The bulky trifluoromethyl group also has a great impact on the binding modes and binding affinities. We believe that our study provides valuable insight into the binding profiles of type I PAMs with alpha 7-nAChR and is helpful for the development of novel PAMs.

Subject headings

NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)
NATURVETENSKAP  -- Kemi -- Organisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Organic Chemistry (hsv//eng)
NATURVETENSKAP  -- Kemi -- Fysikalisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Physical Chemistry (hsv//eng)

Keyword

Teoretisk kemi och biologi
Theoretical Chemistry and Biology

Publication and Content Type

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