Evidence map›Paper›PMID 30041031›Full record

ArticleProtein expression and purification2018

A multi-column plate adapter provides an economical and versatile high-throughput protein purification system.

Matthew J Dominguez, Benjamin J Lantz, Rebecca J Rhode, Zoey L Sharp, Krysten C Finney, Valeria Jaramillo Martinez, Elliott J Stollar

Abstract read
In one paragraph

Article in Protein expression and purification, 2018. 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
0.3field-weighted citation impact, top 43% 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, 10 citations in OpenAlex.

  1. How a highly acidic SH3 domain folds in the absence of its charged peptide target.Protein science : a publication of the Protein Society · 2023
    Article
  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 1 institution in 1 country.

Matthew J DominguezPhysical Sciences Department, Eastern New Mexico University, Portales, NM, USA.
Benjamin J LantzPhysical Sciences Department, Eastern New Mexico University, Portales, NM, USA.
Rebecca J RhodePhysical Sciences Department, Eastern New Mexico University, Portales, NM, USA.
Zoey L SharpPhysical Sciences Department, Eastern New Mexico University, Portales, NM, USA.
Krysten C FinneyPhysical Sciences Department, Eastern New Mexico University, Portales, NM, USA.
Valeria Jaramillo MartinezPhysical Sciences Department, Eastern New Mexico University, Portales, NM, USA.
Elliott J StollarPhysical Sciences Department, Eastern New Mexico University, Portales, NM, USA. Electronic address: e.stollar@liverpool.ac.uk.
Eastern New Mexico University · US

Funding

NM-INBRE Sequencing and Bioinformatics CoreP20GM103451 · NIGMS · NEW MEXICO STATE UNIVERSITY LAS CRUCES · PI Charlotte C. Gard · 2012 to 2026
$61.2M
NIGMS NIH HHS P20 GM103451
6 · The paper itself

Abstract

Protein purification is essential in the study of protein structure and function, and the development of novel therapeutics. Many studies require purifying multiple proteins at once, increasing the demand for improved purification methods. We hypothesized that multiple chromatography columns could be interfaced with a multi-well collection plate for rapid and convenient protein purification without the need of expensive instrumentation. As such, we developed a multi-column plate adapter (MCPA), which provides an economical yet versatile and time efficient, high-throughput protein purification system. The MCPA system simultaneously purified milligrams of different proteins under gravity or under vacuum for faster purification. The MCPA handles up to twenty-four 12 mL columns and multiple MCPA's in sequence allow milligram-scale purification of 96 different samples with relative ease. We also used the MCPA system for large scale affinity purification of four proteins, providing sufficient yields and purity for protein crystallization and biophysical characterization. The MCPA system is ideal for optimizing resin type and volume or any other purification parameter by customizing individual columns during the same purification. The high-throughput and versatile nature of this system should prove to be useful in obtaining adequate amounts of protein for subsequent analyses in any laboratory setting.

Indexed as

Chromatography, AffinityCloning, MolecularEscherichia coliGene ExpressionGenetic VectorsHigh-Throughput Screening AssaysHumansMicrofilament ProteinsMutationPressureProtein DomainsRecombinant ProteinsSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsVacuumABP1 protein, S cerevisiaeMicrofilament ProteinsRecombinant ProteinsSaccharomyces cerevisiae ProteinsHigh-throughputProtein purificationSH3 domain

Identifiers

PMID30041031
PMCPMC6147247
OpenAlexW2883841194

What OpenQuestion holds

Textmetadata
LicenceTDM
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.