Evidence map›Paper›PMID 35889369›Full record

ArticleMolecules (Basel, Switzerland)2022

Protein Attachment Mechanism for Improved Functionalization of Affinity Monolith Chromatography (AMC).

Nayan Nayak, Rosalinda Mazzei, Lidietta Giorno, João G Crespo, Carla A M Portugal, Teresa Poerio

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Nayan NayakLAQV-REQUIMTE, Department of Chemistry, NOVA School of Science and Technology, FCT NOVA, Universidade NOVA de Lisboa, 2829-516 Caparica, Portugal.ORCID 0000-0002-4975-7317
Rosalinda MazzeiInstitute on Membrane Technology, National Research Council, ITM-CNR, Via P. Bucci, 17/C, I87030 Rende, Italy.ORCID 0000-0001-9575-7310
Lidietta GiornoInstitute on Membrane Technology, National Research Council, ITM-CNR, Via P. Bucci, 17/C, I87030 Rende, Italy.ORCID 0000-0002-4408-5849
João G CrespoLAQV-REQUIMTE, Department of Chemistry, NOVA School of Science and Technology, FCT NOVA, Universidade NOVA de Lisboa, 2829-516 Caparica, Portugal.
Carla A M PortugalLAQV-REQUIMTE, Department of Chemistry, NOVA School of Science and Technology, FCT NOVA, Universidade NOVA de Lisboa, 2829-516 Caparica, Portugal.
Teresa PoerioInstitute on Membrane Technology, National Research Council, ITM-CNR, Via P. Bucci, 17/C, I87030 Rende, Italy.ORCID 0000-0001-8449-9344

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This work aims at understanding the attachment mechanisms and stability of proteins on a chromatography medium to develop more efficient functionalization methodologies, which can be exploited in affinity chromatography. In particular, the study was focused on the understanding of the attachment mechanisms of bovine serum albumin (BSA), used as a ligand model, and protein G on novel amine-modified alumina monoliths as a stationary phase. Protein G was used to develop a column for antibody purification. The results showed that, at lower protein concentrations (i.e., 0.5 to 1.0 mg·mL

Indexed as

AntibodiesSerum Albumin, BovineAdsorptionAminesChromatography, AffinityLigandsAminesAntibodiesLigandsSerum Albumin, BovineAPTES functionalizationchromatographyimmunoglobulin G purificationmonolithsprotein-binding kineticsprotein Gprotein immobilization

Identifiers

PMID35889369
PMCPMC9323659

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.