Evidence map›Paper›PMID 30220189›Full record

ArticleIranian biomedical journal2019

Enhancement of Expression Level of Modified t-PA (TNKase) in Leishmania tarentolae by Induction System

Mohammad Mehdi Attarpour Yazdi, Nikky Tofighi, Taraneh Rajaee, Marzieh Ghahremanlou, Ahmad Adeli, Bolhassani Azam, Mohammad Azizi, Noushin Davoudi

Open access · diamondAbstract read
In one paragraph

Article in Iranian biomedical journal, 2019. 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, top 86% 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, 0 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

8 authors at 3 institutions in 1 country.

Mohammad Mehdi Attarpour YazdiDepartment of Microbiology, Faculty of Medicine, Shahed University, Tehran, Iran.
Nikky TofighiBiotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran.
Taraneh RajaeeBiotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran.
Marzieh GhahremanlouBiotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran.
Ahmad AdeliBiotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran.
Bolhassani AzamDepartment of Hepatitis and AIDS, Pasteur Institute of Iran, Tehran, Iran.
Mohammad AziziBiotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran.
Noushin DavoudiBiotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran.
Biotechnology Research Center · IRPasteur Institute of Iran · IRShahed University · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The expression of bio-therapeutic proteins in mammalian cells, such as CHO, attains high homogeneity related to post-translational modifications. Although CHO remains the most popular cell line for bestselling biotherapeutic proteins on the market, there are still drawbacks such as expensive culture media, long time line, and high drug cost. Recently, researches on a novel Leishmania protozoan system have confirmed that this low-level eukaryote could represent a competitive alternative to the mammalian cell lines. Methods: The full length of coding sequence of modified tPA TNKase (tenecteplase) was synthesized and cloned into an inducible expression vector of L. tarentolae T7-TR cells. Results: The expression of the construct was driven by a Tet-inducible promoter. A Leishmania secretory signal sequence was also added to the expression cassette to facilitate the release of the recombinant protein into the medium. The secretory recombinant protein was analyzed and confirmed by SDS-PAGE and Western blot analyses. The expression level of TNKase in this novel system of L. tarentolae was 810 IU/mL after induction, which means that the percentage of expression increases two times compared to previous models in L. tarentolae. The TNKase activity was comparable with Activase. Conclusion: Our results suggested that expressed TNK (modified tPA) is functionally compatible with Activase regarding their effect on fibrinolysis. Given the post-translational modification similarities between mammalian and L. tarentolae, it is speculated that this system is capable of producing complex proteins such as tPA similar to mammalian system, with easier manipulation and non-expensive method.

Indexed as

AmidesAmino Acid SequenceCloning, MolecularLeishmaniaRecombinant ProteinsTenecteplaseAmidesRecombinant ProteinsTenecteplaseLeishmania tarentolaeTenecteplase

Identifiers

PMID30220189
PMCPMC6462294
OpenAlexW2969440610

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.