Evidence map›Paper›PMID 37367650›Full record

ArticleMarine drugs2023

Substitution of D-Arginine at Position 11 of α-RgIA Potently Inhibits α7 Nicotinic Acetylcholine Receptor.

Yong Wu, Junjie Zhang, Jie Ren, Xiaopeng Zhu, Rui Li, Dongting Zhangsun, Sulan Luo

Open access · goldAbstract read
In one paragraph

Article in Marine drugs, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.3field-weighted citation impact, top 37% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Yong WuSchool of Medicine, Guangxi University, Nanning 530004, China.ORCID 0000-0001-6395-4213
Junjie ZhangSchool of Medicine, Guangxi University, Nanning 530004, China.ORCID 0009-0000-3933-820X
Jie RenSchool of Medicine, Guangxi University, Nanning 530004, China.
Xiaopeng ZhuSchool of Medicine, Guangxi University, Nanning 530004, China.ORCID 0000-0001-8830-4954
Rui LiShanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China.
Dongting ZhangsunSchool of Medicine, Guangxi University, Nanning 530004, China.
Sulan LuoSchool of Medicine, Guangxi University, Nanning 530004, China.ORCID 0000-0002-9358-5970
Guangxi University · CNChinese Academy of Sciences · CN

Funding

111 Project D20010Guangxi Science and Technology Base and Talent Special Project 2021AC19001Guangxi Science and Technology Base & Talents Fund GUIKE AD22035948Innovation Project of Guangxi Graduate Education YCSW2022072Major Intergovernmental Joint Re-search Project of National Key R & D Program of China 2022YFE0132700National Natural Science Foundation of China 32170534
6 · The paper itself

Abstract

Conotoxins are a class of disulfide-rich peptides found in the venom of cone snails, which have attracted considerable attention in recent years due to their potent activity on ion channels and potential for therapeutics. Among them, α-conotoxin RgIA, a 13-residue peptide, has shown great promise as a potent inhibitor of α9α10 nAChRs for pain management. In this study, we investigated the effect of substituting the naturally occurring L-type arginine at position 11 of the RgIA sequence with its D-type amino acid. Our results indicate that this substitution abrogated the ability of RgIA to block α9α10 nAChRs, but instead endowed the peptide with the ability to block α7 nAChR activity. Structural analyses revealed that this substitution induced significant alteration of the secondary structure of RgIA[11r], which consequently affected its activity. Our findings underscore the potential of D-type amino acid substitution as a promising strategy for designing novel conotoxin-based ligands targeting different types of nAChRs.

Indexed as

ConotoxinsReceptors, Nicotinicalpha7 Nicotinic Acetylcholine ReceptorArginineNicotinic AntagonistsPeptidesalpha7 Nicotinic Acetylcholine ReceptorArginineConotoxinsNicotinic AntagonistsPeptidesReceptors, NicotinicCD structureconotoxinelectrophysiologynicotinic acetylcholine receptorspeptide synthesis

Identifiers

PMID37367650
PMCPMC10302633
OpenAlexW4378574021

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.