Evidence map›Paper›PMID 18937031›Full record

ArticleJournal of biomolecular NMR2008

Stable-isotope labeling using an inducible viral infection system in suspension-cultured plant cells.

Shinya Ohki, Koji Dohi, Atsushi Tamai, Makoto Takeuchi, Masashi Mori

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of biomolecular NMR, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Protein Delivery into Plant Cells: TowardFrontiers in plant science · 2017
    Article
  7. Article
  8. Article
  9. Article
  10. The structural dynamics of macromolecular processes.Current opinion in cell biology · 2009
    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

5 authors.

Shinya OhkiJapan Advanced Institute of Science and Technology, Center for Nano Materials and Technology, Nomi, Ishikawa, Japan. shinya-o@jaist.ac.jp
Koji Dohi
Atsushi Tamai
Makoto Takeuchi
Masashi Mori

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We established a novel strategy for preparing uniformly stable isotope-labeled proteins by using suspension-cultured plant cells and an inducible virus vector encoding the research target. By using this new method, we demonstrated the expression of three proteins, namely, Escherichia coli dihydrofolate reductase (DHFR), chicken calmodulin (CaM), and porcine protein kinase C-dependent protein phosphatase-1 inhibitor with a molecular mass of 17-kDa (CPI-17). In addition, we successfully expressed bovine pancreatic trypsin inhibitor (BPTI), which contains three pairs of disulfide bonds, as the soluble form. In the most efficient case, as little as 50 ml culture yielded 3-4 mg (15)N-labeled protein suitable for NMR experiments. The (1)H-(15)N HSQC spectra of all of these proteins clearly indicated that their structures were identical to those of their counterparts reported previously. Thus, the present results suggest that our novel protocol is a potential method for NMR sample preparation.

Indexed as

Agrobacterium tumefaciensAprotininCalmodulinCells, CulturedDisulfidesGenetic VectorsIsotope LabelingNicotianaNuclear Magnetic Resonance, BiomolecularPhosphoprotein PhosphatasesRecombinant ProteinsTetrahydrofolate DehydrogenaseTransfectionAprotininCalmodulinDisulfidesPhosphoprotein PhosphatasesRecombinant ProteinsTetrahydrofolate Dehydrogenase

Identifiers

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.