Evidence map›Paper›PMID 10933917›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2000

Metabolic biotinylation of recombinant proteins in mammalian cells and in mice.

M B Parrott, M A Barry

Open access · hybridAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

16 citing papers in PubMed, 59 citations in OpenAlex.

  1. Review
  2. Mammalian Expression andACS omega · 2020
    Article
  3. Review
  4. Article
  5. Selective cell-surface labeling of the molecular motor protein prestin.Biochemical and biophysical research communications · 2011
    Article
  6. Article
  7. Article
  8. Use of protein biotinylation in vivo for immunoelectron microscopic localization of a specific protein isoform.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2008
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Avidin-based targeting and purification of a protein IX-modified, metabolically biotinylated adenoviral vector.Molecular therapy : the journal of the American Society of Gene Therapy · 2004
    Article
  14. Efficient biotinylation and single-step purification of tagged transcription factors in mammalian cells and transgenic mice.Proceedings of the National Academy of Sciences of the United States of America · 2003
    Article
  15. Metabolic biotinylation of recombinant proteins in mammalian cells and in mice.Molecular therapy : the journal of the American Society of Gene Therapy · 2000
    Article
  16. Article
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

2 authors at 2 institutions in 1 country.

M B ParrottDepartment of Microbiology and Immunology, Baylor College of Medicine, Houston, Texas 77030, USA.
M A Barry
Baylor College of Medicine · USRice University · US

Funding

MOLECULAR AND CELLULAR MECHANISMS OF HOST DEFENSET32AI007495 · NIAID · BAYLOR COLLEGE OF MEDICINE · PI TAN, TSE-HUA · 1996 to 2011
$2.4M
NIAID NIH HHS T32 AI007495
6 · The paper itself

Abstract

The avidin-biotin system is a fundamental technology in biomedicine for immunolocalization, imaging, nucleic acid blotting, and protein labeling. While this technology is robust, it is limited by the fact that mammalian proteins must be expressed and purified prior to chemical biotinylation using cross-linking agents which modify proteins at random locations to heterogeneous levels and can inactivate protein function. To circumvent this limitation, we demonstrate the ability to metabolically biotinylate tagged proteins in mammalian cells and in mice using the endogenous biotinylation enzymes of the host. Endogenously biotinylated proteins were readily purified from mammalian cells using monomeric avidin and eluted under nondenaturing conditions using only biotin as the releasing agent. This technology should allow recombinant proteins and fragile protein complexes to be produced and purified from mammalian cells as well as from transgenic plants and animals. In addition, this technology may be particularly useful for cell-targeting applications in which proteins or viral gene therapy vectors can be biotinylated at genetically defined sites for combination with other targeting moieties complexed with avidin.

Indexed as

Amino Acid SequenceAnimalsBase SequenceBiotinCarboxyl and Carbamoyl TransferasesCell LineCHO CellsCricetinaeDNA PrimersFemaleGreen Fluorescent ProteinsHumansLuminescent ProteinsMethodsMiceMice, Inbred BALB CBiotinCarboxyl and Carbamoyl TransferasesDNA PrimersGreen Fluorescent ProteinsLuminescent ProteinsMethylmalonyl-CoA carboxytransferaseRecombinant Fusion Proteins

Identifiers

PMID10933917
PMCPMC2002494
OpenAlexW2113920604

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.