Evidence map›Paper›PMID 27518899›Full record

ArticlePloS one2016

Scalable Production of HPV16 L1 Protein and VLPs from Tobacco Leaves.

Maryam Zahin, Joongho Joh, Sujita Khanal, Adam Husk, Hugh Mason, Heribert Warzecha, Shin-Je Ghim, Donald M Miller, Nobuyuki Matoba, Alfred Bennett Jenson

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
5.1field-weighted citation impact, top 5% 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

20 citing papers in PubMed, 38 citations in OpenAlex.

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  18. LALFPlant biotechnology journal · 2018
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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

10 authors at 4 institutions in 2 countries.

Maryam ZahinJames Graham Brown Cancer Center, University of Louisville, Louisville, Kentucky, United States of America.
Joongho JohJames Graham Brown Cancer Center, University of Louisville, Louisville, Kentucky, United States of America.
Sujita KhanalJames Graham Brown Cancer Center, University of Louisville, Louisville, Kentucky, United States of America.
Adam HuskJames Graham Brown Cancer Center, University of Louisville, Louisville, Kentucky, United States of America.
Hugh MasonBiodesign Institute and School of Life Sciences, Arizona State University, Tempe, Arizona, United States of America.
Heribert WarzechaPlant Biotechnology and Metabolic Engineering, Technische Universita¨t Darmstadt, Schnittspahnstrasse 3-5, 64287, Darmstadt, Germany.
Shin-Je GhimJames Graham Brown Cancer Center, University of Louisville, Louisville, Kentucky, United States of America.
Donald M MillerJames Graham Brown Cancer Center, University of Louisville, Louisville, Kentucky, United States of America.
Nobuyuki MatobaJames Graham Brown Cancer Center, University of Louisville, Louisville, Kentucky, United States of America.
Alfred Bennett JensonJames Graham Brown Cancer Center, University of Louisville, Louisville, Kentucky, United States of America.
James Graham Brown Foundation · USUniversity of Louisville · USArizona State University · USTechnical University of Darmstadt · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cervical cancer is the most common malignancy among women particularly in developing countries, with human papillomavirus (HPV) 16 causing 50% of invasive cervical cancers. A plant-based HPV vaccine is an alternative to the currently available virus-like particle (VLP) vaccines, and would be much less expensive. We optimized methods to express HPV16 L1 protein and purify VLPs from tobacco (Nicotiana benthamiana) leaves transfected with the magnICON deconstructed viral vector expression system. L1 proteins were extracted from agro-infiltrated leaves using a series of pH and salt mediated buffers. Expression levels of L1 proteins and VLPs were verified by immunoblot and ELISA, which confirmed the presence of sequential and conformational epitopes, respectively. Among three constructs tested (16L1d22, TPL1d22, and TPL1F), TPL1F, containing a full-length L1 and chloroplast transit peptide, was best. Extraction of HPV16 L1 from leaf tissue was most efficient (> 2.5% of total soluble protein) with a low-salt phosphate buffer. VLPs were purified using both cesium chloride (CsCl) density gradient and size exclusion chromatography. Electron microscopy studies confirmed the presence of assembled forms of HPV16 L1 VLPs. Collectively; our results indicated that chloroplast-targeted transient expression in tobacco plants is promising for the production of a cheap, efficacious HPV16 L1 VLP vaccine. Studies are underway to develop plant VLPs for the production of a cervical cancer vaccine.

Indexed as

Capsid ProteinsDNA, ViralGenetic EngineeringNicotianaOncogene Proteins, ViralPlant LeavesSafetyVaccines, Virus-Like ParticleCapsid ProteinsDNA, ViralL1 protein, Human papillomavirus type 16Oncogene Proteins, ViralVaccines, Virus-Like Particle

Identifiers

PMID27518899
PMCPMC4982596
OpenAlexW2517366254

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.