Evidence map›Paper›PMID 37329136›Full record

ArticleBiophysical journal2023

Molecular dynamics of mismatch detection-How MutS uses indirect readout to find errors in DNA.

Abhilash Jayaraj, Kelly M Thayer, David L Beveridge, Manju M Hingorani

Open access · hybridAbstract read
In one paragraph

Article in Biophysical journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. DNA Repair Mechanisms.Methods in molecular biology (Clifton, N.J.) · 2027
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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.

Abhilash JayarajChemistry Department, Wesleyan University, Middletown, Connecticut. Electronic address: abhilash.124@gmail.com.
Kelly M ThayerChemistry Department, Wesleyan University, Middletown, Connecticut.
David L BeveridgeChemistry Department, Wesleyan University, Middletown, Connecticut.
Manju M HingoraniMolecular Biology and Biochemistry Department, Wesleyan University, Middletown, Connecticut. Electronic address: mhingorani@wesleyan.edu.
Wesleyan University · US

Funding

Ensemble Networks for Allosteric Drug DesignR15GM128102 · NIGMS · WESLEYAN UNIVERSITY · PI THAYER, KELLY MARIE · 2018 to 2021
$976k
An MD-MSM Study of Allosterism on the DNA Repair Protein MutSR15GM129715 · NIGMS · WESLEYAN UNIVERSITY · PI BEVERIDGE, DAVID LEWIS · 2018 to 2018
$488k
Librational Mode Coupling Theory of Allosteric Signal TransmissionR15GM144870 · NIGMS · WESLEYAN UNIVERSITY · PI BEVERIDGE, DAVID LEWIS · 2022 to 2022
$482k
Investigation of defective allosteric signaling as a basis for DNA mismatch repair malfunction in Lynch cancer syndromeR15GM114743 · NIGMS · WESLEYAN UNIVERSITY · PI HINGORANI, MANJU M · 2015 to 2015
$409k
NIGMS NIH HHS R15 GM114743NIGMS NIH HHS R15 GM128102NIGMS NIH HHS R15 GM129715NIGMS NIH HHS R15 GM144870
6 · The paper itself

Abstract

The mismatch repair protein MutS safeguards genomic integrity by finding and initiating repair of basepairing errors in DNA. Single-molecule studies show MutS diffusing on DNA, presumably scanning for mispaired/unpaired bases, and crystal structures show a characteristic "mismatch-recognition" complex with DNA enclosed within MutS and kinked at the site of error. But how MutS goes from scanning thousands of Watson-Crick basepairs to recognizing rare mismatches remains unanswered, largely because atomic-resolution data on the search process are lacking. Here, 10 μs all-atom molecular dynamics simulations of Thermus aquaticus MutS bound to homoduplex DNA and T-bulge DNA illuminate the structural dynamics underlying the search mechanism. MutS-DNA interactions constitute a multistep mechanism to check DNA over two helical turns for its 1) shape, through contacts with the sugar-phosphate backbone, 2) conformational flexibility, through bending/unbending engineered by large-scale motions of the clamp domain, and 3) local deformability, through basepair destabilizing contacts. Thus, MutS can localize a potential target by indirect readout due to lower energetic costs of bending mismatched DNA and identify a site that distorts easily due to weaker base stacking and pairing as a mismatch. The MutS signature Phe-X-Glu motif can then lock in the mismatch-recognition complex to initiate repair.

Indexed as

Escherichia coli ProteinsMolecular Dynamics SimulationBase PairingBase Pair MismatchDNAMutS DNA Mismatch-Binding ProteinDNAEscherichia coli ProteinsMutS DNA Mismatch-Binding Protein

Identifiers

PMID37329136
PMCPMC10432192
OpenAlexW4380758629

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.