Evidence map›Paper›PMID 30930630›Full record

ArticleTurkish journal of biology = Turk biyoloji dergisi2019

Protein engineering approaches for antibody fragments: directed evolution and rational design approaches.

Merve Arslan, Dilara Karadağ, Sibel Kalyoncu

Abstract read
In one paragraph

Article in Turkish journal of biology = Turk biyoloji dergisi, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Reducing Immunogenicity by Design: Approaches to Minimize Immunogenicity of Monoclonal Antibodies.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2024
    Review
  5. The application of adenine deaminase in antibody affinity maturation.Applied microbiology and biotechnology · 2023
    Article
  6. Article
  7. Protein-based lateral flow assays for COVID-19 detection.Protein engineering, design & selection : PEDS · 2021
    Review
  8. Review
  9. Article
  10. Article
  11. 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

3 authors.

Merve Arslanİzmir Biomedicine and Genome Center , İzmir , Turkey.ORCID 0000-0002-6135-510X
Dilara Karadağİzmir Biomedicine and Genome Center , İzmir , Turkey.ORCID 0000-0002-4635-3771
Sibel Kalyoncuİzmir Biomedicine and Genome Center , İzmir , Turkey.ORCID 0000-0003-2264-0757

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The number of therapeutic antibodies in preclinical, clinical, or approved phases has been increasing exponentially, mostly due to their known successes. Development of antibody engineering methods has substantially hastened the development of therapeutic antibodies. A variety of protein engineering techniques can be applied to antibodies to improve their afinity and/or biophysical properties such as solubility and stability. Antibody fragments (where all or some parts of constant regions are eliminated while the essential antigen binding region is preserved) are more suitable for protein engineering techniques because there are many in vitro screening technologies available for antibody fragments but not full-length antibodies. Improvement of biophysical characteristics is important in the early development phase because most antibodies fail at the later stage of development and this leads to loss of resources and time. Here, we review directed evolution and rational design methods to improve antibody properties. Recent developments in rational design approaches and antibody display technologies, and especially phage display, which was recently awarded the 2018 Nobel Prize, are discussed to be used in antibody research and development.

Indexed as

afinityAntibodyantibody fragmentbiophysical propertiesdirected evolutionphage displayprotein engineeringrational designyeast surface display

Identifiers

PMID30930630
PMCPMC6426644

What OpenQuestion holds

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Registered trials

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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.