Evidence map›Paper›PMID 36334045›Full record

ArticleProtein science : a publication of the Protein Society2022

Application of biophysical methods for improved protein production and characterization: A case study on an high-temperature requirement A-family bacterial protease.

Michael Ronzetti, Bolormaa Baljinnyam, Ishrat Jalal, Utpal Pal, Anton Simeonov

Open access · bronzeAbstract read
In one paragraph

Article in Protein science : a publication of the Protein Society, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 35% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. 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

5 authors at 3 institutions in 2 countries.

Michael RonzettiNational Center for Advancing Translational Sciences, National Institutes of Health, Rockville, Maryland, USA.ORCID 0000-0001-5034-7692
Bolormaa BaljinnyamNational Center for Advancing Translational Sciences, National Institutes of Health, Rockville, Maryland, USA.ORCID 0000-0001-9548-4965
Ishrat JalalNanoTemper Technologies GmbH, Munich, Germany.
Utpal PalDepartment of Veterinary Medicine, College of Agriculture & Natural Resources, University of Maryland, College Park, Maryland, USA.ORCID 0000-0002-7504-4628
Anton SimeonovNational Center for Advancing Translational Sciences, National Institutes of Health, Rockville, Maryland, USA.ORCID 0000-0002-4523-9977
National Institutes of Health · USNanoTemper Technologies (Germany) · DEUniversity of Maryland, College Park · US

Funding

BORRELIA GENE PRODUCTS CRITICAL FOR NATURAL INFECTION CYCLER01AI080615 · NIAID · UNIV OF MARYLAND, COLLEGE PARK · PI PAL, UTPAL · 2009 to 2024
$5.2M
NIAID NIH HHS R01 AI080615
6 · The paper itself

Abstract

The high-temperature requirement A (HtrA) serine protease family presents an attractive target class for antibacterial therapeutics development. These proteins possess dual protease and chaperone functions and contain numerous binding sites and regulatory loops, displaying diverse oligomerization patterns dependent on substrate type and occupancy. HtrA proteins that are natively purified coelute with contaminating peptides and activating species, shifting oligomerization and protein structure to differently activated populations. Here, a redesigned HtrA production results in cleaner preparations with high yields by overexpressing and purifying target protein from inclusion bodies under denaturing conditions, followed by a high-throughput screen for optimal refolding buffer composition using function-agnostic biophysical techniques that do not rely on target-specific measurements. We use Borrelia burgdorferi HtrA to demonstrate the effectiveness of our function-agnostic approach, while characterization with both new and established biophysical methods shows the retention of proteolytic and chaperone activity of the refolded protein. This systematic workflow and toolset will translate to the production of HtrA-family proteins in higher quantities of pure and monodisperse composition than the current literature standard, with applicability to a broad array of protein purification strategies.

Indexed as

Borrelia burgdorferiSerine EndopeptidasesBacteriaBacterial ProteinsMolecular ChaperonesSerine ProteasesTemperatureBacterial ProteinsMolecular ChaperonesSerine EndopeptidasesSerine Proteasesbuffer screeningdifferential scanning fluorimetryhigh-throughput screeningHtrAprotein purificationprotein refolding

Identifiers

PMID36334045
PMCPMC9679970
OpenAlexW4308256891

What OpenQuestion holds

Textmetadata
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.