Evidence map›Paper›PMID 33934257›Full record

ArticleBiotechnology letters2021

Expression cassette and plasmid construction for Yeast Surface Display in Saccharomyces cerevisiae.

Renan Eugênio Araujo Piraine, Vitória Sequeira Gonçalves, Alceu Gonçalves Dos Santos Junior, Rodrigo Casquero Cunha, Pedro Machado Medeiros de Albuquerque, Neida Lucia Conrad, Fábio Pereira Leivas Leite

Abstract read
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In one paragraph

Article in Biotechnology letters, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Review
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.

Renan Eugênio Araujo PiraineNúcleo de Biotecnologia, Centro de Desenvolvimento Tecnológico, Universidade Federal de Pelotas, Pelotas, RS, Brazil.ORCID http://orcid.org/0000-0001-6650-8286
Vitória Sequeira GonçalvesNúcleo de Biotecnologia, Centro de Desenvolvimento Tecnológico, Universidade Federal de Pelotas, Pelotas, RS, Brazil.ORCID http://orcid.org/0000-0003-1639-2494
Alceu Gonçalves Dos Santos JuniorNúcleo de Biotecnologia, Centro de Desenvolvimento Tecnológico, Universidade Federal de Pelotas, Pelotas, RS, Brazil.ORCID http://orcid.org/0000-0001-6687-2619
Rodrigo Casquero CunhaNúcleo de Biotecnologia, Centro de Desenvolvimento Tecnológico, Universidade Federal de Pelotas, Pelotas, RS, Brazil.ORCID http://orcid.org/0000-0003-0145-0321
Pedro Machado Medeiros de AlbuquerqueNúcleo de Biotecnologia, Centro de Desenvolvimento Tecnológico, Universidade Federal de Pelotas, Pelotas, RS, Brazil.ORCID http://orcid.org/0000-0001-9311-6050
Neida Lucia ConradNúcleo de Biotecnologia, Centro de Desenvolvimento Tecnológico, Universidade Federal de Pelotas, Pelotas, RS, Brazil.ORCID http://orcid.org/0000-0001-7573-0794
Fábio Pereira Leivas LeiteNúcleo de Biotecnologia, Centro de Desenvolvimento Tecnológico, Universidade Federal de Pelotas, Pelotas, RS, Brazil. fleivasleite@gmail.com.ORCID http://orcid.org/0000-0003-0941-7286
Universidade Federal de Pelotas · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesDevelop a Cell Surface Display system in Saccharomyces cerevisiae, based on the construction of an expression cassette for pYES2 plasmid.

resultsThe construction of an expression cassette containing the α-factor signal peptide and the C-terminal portion of the α-agglutinin protein was made and its sequence inserted into a plasmid named pYES2/gDαAgglutinin. The construction allows surface display of bovine herpesvirus type 5 (BoHV-5) glycoprotein D (gD) on S. cerevisiae BY4741 strain. Recombinant protein expression was confirmed by dot blot, and indirect immunofluorescence using monoclonal anti-histidine antibodies and polyclonal antibodies from mice experimentally vaccinated with a recombinant gD.

conclusionsThese results demonstrate that the approach and plasmid used represent not only an effective system for immobilizing proteins on the yeast cell surface, as well as a platform for immunobiologicals development.

Indexed as

Recombinant Fusion ProteinsAnimalsCell Surface Display TechniquesMicePlasmidsSaccharomyces cerevisiaeViral Envelope Proteinsglycoprotein D, bovine herpesvirus 5Recombinant Fusion ProteinsViral Envelope ProteinsGlycoprotein DpYES2/gDαAgglutininSaccharomyces cerevisiaeYeast Surface Display

Identifiers

PMID33934257
OpenAlexW3133071551

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.