Evidence map›Paper›PMID 38494245›Full record

ArticleJournal, genetic engineering & biotechnology2024

Expression and scale-up production of recombinant human papillomavirus type 52 L1 protein in methylotrophic yeast Hansenula polymorpha.

Sheila Chairunnisa, Apon Zaenal Mustopa, Budiman Bela, Moh Egy Rahman Firdaus, Shasmita Irawan, Rosyida Khusniatul Arifah, Herman Irawan, Maritsa Nurfatwa, Rifqiyah Nur Umami, Nurlaili Ekawati and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Journal, genetic engineering & biotechnology, 2024. 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
0.5field-weighted citation impact, top 39% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

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

12 authors at 4 institutions in 1 country.

Sheila ChairunnisaMaster's Programme in Biomedical Sciences, Faculty of Medicine Universitas Indonesia, Jakarta 10430, Indonesia; Research Center for Genetic Engineering, National Research and Innovation Agency (BRIN), Bogor 16911, Indonesia.
Apon Zaenal MustopaResearch Center for Genetic Engineering, National Research and Innovation Agency (BRIN), Bogor 16911, Indonesia. Electronic address: azmustopa@yahoo.com.
Budiman BelaDepartment of Microbiology, Faculty of Medicine, Universitas Indonesia, Jakarta, Indonesia.
Moh Egy Rahman FirdausResearch Center for Genetic Engineering, National Research and Innovation Agency (BRIN), Bogor 16911, Indonesia.
Shasmita IrawanResearch Center for Genetic Engineering, National Research and Innovation Agency (BRIN), Bogor 16911, Indonesia.
Rosyida Khusniatul ArifahResearch Center for Genetic Engineering, National Research and Innovation Agency (BRIN), Bogor 16911, Indonesia.
Herman IrawanResearch Center for Genetic Engineering, National Research and Innovation Agency (BRIN), Bogor 16911, Indonesia.
Maritsa NurfatwaResearch Center for Genetic Engineering, National Research and Innovation Agency (BRIN), Bogor 16911, Indonesia.
Rifqiyah Nur UmamiResearch Center for Genetic Engineering, National Research and Innovation Agency (BRIN), Bogor 16911, Indonesia.
Nurlaili EkawatiResearch Center for Genetic Engineering, National Research and Innovation Agency (BRIN), Bogor 16911, Indonesia.
Ai HertatiResearch Center for Genetic Engineering, National Research and Innovation Agency (BRIN), Bogor 16911, Indonesia.
Nurhasni HasanFaculty of Pharmacy, Universitas Hasanuddin, Jl. Perintis Kemerdekaan Km 10, Makassar 90245, Indonesia. Electronic address: Nurhasni.hasan@unhas.ac.id.
National Research and Innovation AgencyIndonesian Agency for Agricultural Research and Development · IDUniversity of Indonesia · IDHasanuddin University · ID

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHuman papillomavirus (HPV) vaccination is one of the crucial national vaccination programs aimed at reducing the prevalence of the diseases associated with HPV infections, which continue to pose a global health concern. However, a significant disparity exists in the distribution of HPV vaccine, particularly in low-middle income countries where the cost of HPV vaccine becomes a major obstacle. Thus, it is essential to ensure the availability of an economically feasible HPV vaccine, necessitating immediate efforts to enhance the cost-effectiveness of vaccine production. This study aimed to develop an efficient production system for the recombinant HPV type 52 L1 protein as HPV vaccine material using methylotrophic yeast Hansenula polymorpha expression system.

resultsThis study presents an in-depth examination of the expression and scale-up production of HPV type 52 L1 protein using DASGIP® parallel bioreactor system. The pHIPX4 plasmid, which is regulated by the MOX promoter, generates stable clones that express the target protein. Cultivation employing the synthetic medium SYN6(10) with controlled parameters (e.g. temperature, pH, feeding strategy, and aeration) produces 0.15 µg/mL of HPV type 52 L1 protein, suggesting a possibility for scaling up to a higher production level.

conclusionThe scale-up production of HPV type 52 L1 protein using Hansenula polymorpha expression system described in this study provides an opportunity for an economical manufacturing platform for the development of the HPV vaccine.

Indexed as

DASGIP® parallel bioreactor systemHansenula polymorphaHPV type 52 L1 proteinSynthetic medium

Identifiers

PMID38494245
PMCPMC10903760
OpenAlexW4391765047

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.