Evidence map›Paper›PMID 42020898›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2026

Selecting Novel Retino-tropic AAV Capsids by Directed Evolution.

Adrian Westhaus, Leszek Lisowski

Abstract read
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Article in Methods in molecular biology (Clifton, N.J.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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.

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

2 authors.

Adrian WesthausTranslational Vectorology Research Unit, Children's Medical Research Institute, Faculty of Medicine and Health, The University of Sydney, Westmead, NSW, Australia.
Leszek LisowskiTranslational Vectorology Research Unit, Children's Medical Research Institute, Faculty of Medicine and Health, The University of Sydney, Westmead, NSW, Australia. llisowski@cmri.org.au.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The selection of novel AAV variants for retinal transduction has been successful for several model systems in the past. Despite this, the publication of a full directed evolution protocol that explains all steps from basic library generation techniques to the selection of suitable candidates for further testing is lacking. The following methods chapter provides a detailed protocol for the generation of an AAV library and the recovery of the most functional candidates using highly predictive transgene expression-driven selection platform. It is important to note that multiple selection platforms have been developed to date, each with unique set of strengths and weaknesses. However, the choice of a selection platform most suitable for given AAV bioengineering application is beyond the scope of this chapter. For the purpose of this chapter, we will describe steps involved in generation of an exemplar peptide insertion library into the variable region VIII of the AAV2 capsid, but the steps outlined can be extended to all other serotypes and other surface loops. Furthermore, the technologies described work independently of the model system and do not require any major specialist equipment.

Indexed as

CapsidCapsid ProteinsDependovirusDirected Molecular EvolutionGenetic VectorsGene LibraryHumansPeptide LibraryTransduction, GeneticCapsid ProteinsPeptide LibraryAAVCapsid library selectionDirected evolutionGene therapyViral vector production

Identifiers

PMID42020898

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.