Evidence map›Paper›PMID 38129631›Full record

ArticleMikrochimica acta2023

Immobilization of azide-functionalized proteins to micro- and nanoparticles directly from cell lysate.

Gunjan Saini, Mrugesh Krishna Parasa, Katherine N Clayton, Julia G Fraseur, Scott C Bolton, Kevin P Lin, Steven T Wereley, Tamara L Kinzer-Ursem

Open access · hybridAbstract read
In one paragraph

Article in Mikrochimica acta, 2023. 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
0.5field-weighted citation impact, top 32% 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, 3 citations in OpenAlex.

  1. Article
  2. Review
  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

8 authors at 1 institution in 1 country.

Gunjan SainiWeldon School of Biomedical Engineering, Purdue University, West Lafayette, IN, 47906, USA.
Mrugesh Krishna ParasaWeldon School of Biomedical Engineering, Purdue University, West Lafayette, IN, 47906, USA.
Katherine N ClaytonSchool of Mechanical Engineering, Purdue University, West Lafayette, IN, 47906, USA.
Julia G FraseurWeldon School of Biomedical Engineering, Purdue University, West Lafayette, IN, 47906, USA.
Scott C BoltonWeldon School of Biomedical Engineering, Purdue University, West Lafayette, IN, 47906, USA.
Kevin P LinDepartment of Biochemistry, Purdue University, West Lafayette, IN, 47906, USA.
Steven T WereleySchool of Mechanical Engineering, Purdue University, West Lafayette, IN, 47906, USA.
Tamara L Kinzer-UrsemWeldon School of Biomedical Engineering, Purdue University, West Lafayette, IN, 47906, USA. tursem@purdue.edu.ORCID 0000-0001-7343-115X
Purdue University West Lafayette · US

Funding

Protein Tagging for High Resolution Structural Analysis of Synaptic Protein Complexes Using Clickable CryoEM GridsR21NS095218 · NINDS · PURDUE UNIVERSITY · PI KINZER-URSEM, TAMARA L · 2016 to 2017
$404k
NIH HHS 5R21NS095218NINDS NIH HHS R21 NS095218
6 · The paper itself

Abstract

Immobilization of proteins and enzymes on solid supports has been utilized in a variety of applications, from improved protein stability on supported catalysts in industrial processes to fabrication of biosensors, biochips, and microdevices. A critical requirement for these applications is facile yet stable covalent conjugation between the immobilized and fully active protein and the solid support to produce stable, highly bio-active conjugates. Here, we report functionalization of solid surfaces (gold nanoparticles and magnetic beads) with bio-active proteins using site-specific and biorthogonal labeling and azide-alkyne cycloaddition, a click chemistry. Specifically, we recombinantly express and selectively label calcium-dependent proteins, calmodulin and calcineurin, and cAMP-dependent protein kinase A (PKA) with N-terminal azide-tags for efficient conjugation to nanoparticles and magnetic beads. We successfully immobilized the proteins on to the solid supports directly from the cell lysate with click chemistry, forgoing the step of purification. This approach is optimized to yield low particle aggregation and high levels of protein activity post-conjugation. The entire process enables streamlined workflows for bioconjugation and highly active conjugated proteins.

Indexed as

AzidesMetal NanoparticlesCatalysisGoldProteinsAzidesGoldProteinsCalcineurinCalmodulinClick chemistryGold nanoparticlesMagnetic beadsProtein kinase AProtein labeling

Identifiers

PMID38129631
PMCPMC10739308
OpenAlexW4390078579

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.