Evidence map›Paper›PMID 9342313›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1997

Making chemistry selectable by linking it to infectivity.

C Gao, C H Lin, C H Lo, S Mao, P Wirsching, R A Lerner, K D Janda

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
6.8field-weighted citation impact, top 3% 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

13 citing papers in PubMed, 61 citations in OpenAlex.

  1. Antibody selection using clonal cocultivation ofProceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  2. Phenotype-information-phenotype cycle for deconvolution of combinatorial antibody libraries selected against complex systems.Proceedings of the National Academy of Sciences of the United States of America · 2011
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Toward cocaine esterase therapeutics.Journal of the American Chemical Society · 2005
    Article
  8. Treating cocaine addiction with viruses.Proceedings of the National Academy of Sciences of the United States of America · 2004
    Article
  9. A method for the generation of combinatorial antibody libraries using pIX phage display.Proceedings of the National Academy of Sciences of the United States of America · 2002
    Article
  10. Article
  11. Article
  12. Making artificial antibodies: a format for phage display of combinatorial heterodimeric arrays.Proceedings of the National Academy of Sciences of the United States of America · 1999
    Article
  13. A method for directed evolution and functional cloning of enzymes.Proceedings of the National Academy of Sciences of the United States of America · 1998
    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

7 authors at 1 institution in 1 country.

C GaoDepartment of Chemistry, The Scripps Research Institute and The Skaggs Institute for Chemical Biology, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
C H Lin
C H Lo
S Mao
P Wirsching
R A Lerner
K D Janda
Scripps Research Institute · US

Funding

TUMORICIDAL ACTIVITY OF HOST COMPLEMENTP01CA027489 · NCI · SCRIPPS RESEARCH INSTITUTE · PI LERNER, RICHARD ALAN · 1985 to 2004
$7.7M
CATALYTIC ANTIBODIESR01GM043858 · NIGMS · SCRIPPS RESEARCH INSTITUTE · PI JANDA, KIM D · 1995 to 2002
$459k
CATALYTIC ANTIBODIESR29GM043858 · NIGMS · SCRIPPS RESEARCH INSTITUTE · PI JANDA, KIM D · 1990 to 1994
–
NCI NIH HHS P01 CA027489NCI NIH HHS P01CA27489-16NIGMS NIH HHS GM 43858
6 · The paper itself

Abstract

The link between recognition and replication is fundamental to the operation of the immune system. In recent years, modeling this process in a format of phage-display combinatorial libraries has afforded a powerful tool for obtaining valuable antibodies. However, the ability to readily select and isolate rare catalysts would expand the scope of library technology. A technique in which phage infection controlled the link between recognition and replication was applied to show that chemistry is a selectable process. An antibody that operated by covalent catalysis to form an acyl intermediate restored phage infectivity and allowed selection from a library in which the catalyst constituted 1 in 10(5) members. Three different selection approaches were examined for their convenience and generality. Incorporating these protocols together with well known affinity labels and mechanism-based inactivators should allow the procurement of a wide range of novel catalytic antibodies.

Indexed as

Peptide LibrarySelection, GeneticAntibodies, CatalyticBacteriophagesBase SequenceHelper VirusesImmunoglobulin FragmentsImmunoglobulin Variable RegionMolecular BiologyMolecular Sequence DataRecombinant Fusion ProteinsAntibodies, CatalyticImmunoglobulin FragmentsImmunoglobulin Variable RegionPeptide LibraryRecombinant Fusion Proteins

Identifiers

PMID9342313
PMCPMC23570
OpenAlexW2079274115

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.