Evidence map›Paper›PMID 37815721›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2024

Structural Determination of Glucosyltransferase C by Cryo-Electron Microscopy.

Qing Xie, Jianhao Cao, Hua Zhang, Hui Wu

Open access · greenAbstract read
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 61% 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

1 citing paper in PubMed, 0 citations in OpenAlex.

  1. Article
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

4 authors at 1 institution in 1 country.

Qing XieDepartments of Integrative Biomedical Sciences and Chemical Physiology and Biochemistry, Oregon Health & Science University, Portland, OR, USA.
Jianhao CaoDepartments of Integrative Biomedical Sciences and Chemical Physiology and Biochemistry, Oregon Health & Science University, Portland, OR, USA.
Hua ZhangDepartments of Integrative Biomedical Sciences and Chemical Physiology and Biochemistry, Oregon Health & Science University, Portland, OR, USA.
Hui WuDepartments of Integrative Biomedical Sciences and Chemical Physiology and Biochemistry, Oregon Health & Science University, Portland, OR, USA. wuhu@ohsu.edu.
Oregon Health & Science University · US

Funding

Pacific Northwest Center for Cryo-EM - Screening supplementU24GM129547 · NIGMS · OREGON HEALTH & SCIENCE UNIVERSITY · PI EVANS, JAMES E, GOUAUX, JAMES E · 2018 to 2023
$54.8M
BrpA in Virulence Modulation of Streptococcus mutansR01DE019452 · NIDCR · LSU HEALTH SCIENCES CENTER · PI ZEZHANG TOM WEN, Hui Wu · 2009 to 2026
$6.3M
Glycosylation & Function of an Oral Streptococcal AdhesinR01DE017954 · NIDCR · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI WU, HUI · 2007 to 2022
$5.8M
SMALL MOLECULE INHIBITORS OF CARIOGENIC BIOFILMSR01DE022350 · NIDCR · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Christian Corey Melander, Hui Wu · 2012 to 2026
$4.3M
Structural and Functional Studies on the Glucosyltransferases of the Dental Caries Pathogen Streptococcus mutansR01DE033232 · NIDCR · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Champion Christdoss Selvakumar Deivanayagam, Hui Wu · 2024 to 2026
$1.9M
BACTERIAL SECOND MESSENGER MEDIATED VIRULENCE REGULATION IN STREPTOCOCCUS MUTANSR01DE028329 · NIDCR · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI WU, HUI · 2019 to 2023
$1.7M
Training in structural biology & glycobiologyF33DE022215 · NIDCR · IMPERIAL COLLEGE OF SCIENCE, TECHNOLOGY AND MEDICINE · PI WU, HUI · 2012 to 2012
$64k
NIDCR NIH HHS F33 DE022215NIDCR NIH HHS R01 DE017954NIDCR NIH HHS R01 DE019452NIDCR NIH HHS R01 DE022350NIDCR NIH HHS R01 DE028329NIDCR NIH HHS R01 DE033232NIGMS NIH HHS U24 GM129547
6 · The paper itself

Abstract

Biofilm formation is a critical factor in the development of cariogenic virulence of Streptococcus mutans. S. mutans has evolved a concerted mechanism to synthesize a biofilm matrix from dietary sugars by a family of glucosyltransferases (Gtfs). Three Gtfs, GtfB, C, and D utilize sucrose to form a sticky polymer consisting of insoluble and soluble glucans, a biofilm foundation. Each Gtf possesses two distinct domains, an N-terminal enzyme catalytic domain and a C-terminal glucan binding domain. X-ray crystallographic studies have determined a three-dimensional structure of the catalytic domain of GtfC, however, the structure of the C-terminal domain and the overall structure of Gtfs are unknown. Here, we provided a protocol that will guide us to solve Gtf structures using cryo-electron microscopy (cryo-EM). Cryo-EM and X-ray crystallography are two widely used techniques for determining protein structures, and both methods have their own advantages and limitations. Additionally, we also predicted the full-length GtfC structural using AlphaFold2. Overall, the combination of AlphaFold 2 with experimental approaches offers a powerful and synergistic strategy for protein structure determination, accelerating the pace of scientific discovery and enabling new insights into the molecular basis that govern the biosynthetic activities of Gtfs, which may inform the design of more effective treatments for cariogenic biofilms and associated diseases.

Indexed as

GlucosyltransferasesStreptococcus mutansBiofilmsCryoelectron MicroscopyGlucansProteinsGlucansglucosyltransferase CGlucosyltransferasesProteinsAlpha foldCryo-electron microscopyGlucosyltransferaseStreptococcus mutansStructural determination

Identifiers

PMID37815721
PMCPMC12289283
OpenAlexW4387472936

What OpenQuestion holds

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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.