Evidence map›Paper›PMID 35427450›Full record

ArticleJournal of the American Chemical Society2022

Recipes for Inducing Cold Denaturation in an Otherwise Stable Protein.

Angela Bitonti, Rita Puglisi, Massimiliano Meli, Stephen R Martin, Giorgio Colombo, Piero Andrea Temussi, Annalisa Pastore

Open access · hybridAbstract read
In one paragraph

Article in Journal of the American Chemical Society, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.0field-weighted citation impact, top 27% 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

3 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

7 authors at 4 institutions in 2 countries.

Angela BitontiDepartment of Molecular Medicine, University of Pavia, Via C Forlanini 6, 27100 Pavia, Italy.
Rita PuglisiUK Dementia Research Institute at the Maurice Wohl Institute of King's College London, London SE5 9RT, United Kingdom.ORCID 0000-0002-2980-442X
Massimiliano MeliIstituto di Scienze e Tecnologie Chimiche "Giulio Natta" (SCITEC), CNR, Via Mario Bianco 9, 20131 Milano, Italy.ORCID 0000-0003-3304-6104
Stephen R MartinStructural Biology Technology Platform, The Francis Crick Institute, 1 Midland Rd, London NW1 1AT, United Kingdom.
Giorgio ColomboDepartment of Chemistry, University of Pavia, Via Torquato Taramelli, 12, Pavia 27100, Italy.ORCID 0000-0002-1318-668X
Piero Andrea TemussiUK Dementia Research Institute at the Maurice Wohl Institute of King's College London, London SE5 9RT, United Kingdom.ORCID 0000-0001-6032-4291
Annalisa PastoreUK Dementia Research Institute at the Maurice Wohl Institute of King's College London, London SE5 9RT, United Kingdom.ORCID 0000-0002-3047-654X
King's College London · GBUniversity of Pavia · ITIstituto di Chimica Biomolecolare · ITThe Francis Crick Institute · GB

Funding

Medical Research Council
6 · The paper itself

Abstract

Although cold denaturation is a fundamental phenomenon common to all proteins, it can only be observed in a handful of cases where it occurs at temperatures above the freezing point of water. Understanding the mechanisms that determine cold denaturation and the rules that permit its observation is an important challenge. A way to approach them is to be able to induce cold denaturation in an otherwise stable protein by means of mutations. Here, we studied CyaY, a relatively stable bacterial protein with no detectable cold denaturation and a high melting temperature of 54 °C. We have characterized for years the yeast orthologue of CyaY, Yfh1, a protein that undergoes cold and heat denaturation at 5 and 35 °C, respectively. We demonstrate that, by transferring to CyaY the lessons learnt from Yfh1, we can induce cold denaturation by introducing a restricted number of carefully designed mutations aimed at destabilizing the overall fold and inducing electrostatic frustration. We used molecular dynamics simulations to rationalize our findings and demonstrate the individual effects observed experimentally with the various mutants. Our results constitute the first example of rationally designed cold denaturation and demonstrate the importance of electrostatic frustration on the mechanism of cold denaturation.

Indexed as

Cold TemperatureProteinsHot TemperatureMolecular Dynamics SimulationProtein DenaturationThermodynamicsProteins

Identifiers

PMID35427450
PMCPMC9052743
OpenAlexW4223967616

What OpenQuestion holds

Textmetadata
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.