Evidence map›Paper›PMID 38523412›Full record

ArticleThe FEBS journal2024

A novel pathological mutant reveals the role of torsional flexibility in the serpin breach in adoption of an aggregation-prone intermediate.

Kamila Kamuda, Riccardo Ronzoni, Avik Majumdar, Fiona H X Guan, James A Irving, David A Lomas

Open access · hybridAbstract read
In one paragraph

Article in The FEBS journal, 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
1.1field-weighted citation impact, top 23% 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, 4 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

6 authors at 3 institutions in 2 countries.

Kamila KamudaDivision of Medicine, UCL Respiratory, Rayne Institute, University College London, UK.ORCID 0000-0002-3511-5823
Riccardo RonzoniDivision of Medicine, UCL Respiratory, Rayne Institute, University College London, UK.ORCID 0000-0002-3981-8104
Avik MajumdarAW Morrow Gastroenterology and Liver Centre, Royal Prince Alfred Hospital, Sydney, Australia.ORCID 0000-0003-2975-4327
Fiona H X GuanAW Morrow Gastroenterology and Liver Centre, Royal Prince Alfred Hospital, Sydney, Australia.
James A IrvingDivision of Medicine, UCL Respiratory, Rayne Institute, University College London, UK.ORCID 0000-0003-3204-6356
David A LomasDivision of Medicine, UCL Respiratory, Rayne Institute, University College London, UK.ORCID 0000-0003-2339-6979
Institute of Structural and Molecular Biology · GBRoyal Prince Alfred Hospital · AUThe University of Melbourne · AU

Funding

Alpha-1 Foundation 1036784Medical Research Council MR/NO24842/1Medical Research Council MR/V034243/1UCLH Biomedical Research CentreWellcome TrustWellcome Trust 219939/Z/19/Z
6 · The paper itself

Abstract

Mutants of alpha-1-antitrypsin cause the protein to self-associate and form ordered aggregates ('polymers') that are retained within hepatocytes, resulting in a predisposition to the development of liver disease. The associated reduction in secretion, and for some mutants, impairment of function, leads to a failure to protect lung tissue against proteases released during the inflammatory response and an increased risk of emphysema. We report here a novel deficiency mutation (Gly192Cys), that we name the Sydney variant, identified in a patient in heterozygosity with the Z allele (Glu342Lys). Cellular analysis revealed that the novel variant was mostly retained as insoluble polymers within the endoplasmic reticulum. The basis for this behaviour was investigated using biophysical and structural techniques. The variant showed a 40% reduction in inhibitory activity and a reduced stability as assessed by thermal unfolding experiments. Polymerisation involves adoption of an aggregation-prone intermediate and paradoxically the energy barrier for transition to this state was increased by 16% for the Gly192Cys variant with respect to the wild-type protein. However, with activation to the intermediate state, polymerisation occurred at a 3.8-fold faster rate overall. X-ray crystallography provided two crystal structures of the Gly192Cys variant, revealing perturbation within the 'breach' region with Cys192 in two different orientations: in one structure it faces towards the hydrophobic core while in the second it is solvent-exposed. This orientational heterogeneity was confirmed by PEGylation. These data show the critical role of the torsional freedom imparted by Gly192 in inhibitory activity and stability against polymerisation.

Indexed as

alpha 1-AntitrypsinCrystallography, X-RayEndoplasmic ReticulumHumansModels, MolecularMutationProtein AggregatesProtein Aggregation, PathologicalProtein Conformationalpha 1-AntitrypsinProtein AggregatesSERPINA1 protein, humanalpha‐1‐antitrypsinalpha‐1‐antitrypsin deficiencyconformational diseaseprotein foldingserpin

Identifiers

PMID38523412
PMCPMC11753496
OpenAlexW4393155158

What OpenQuestion holds

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LicenceCC BY
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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.