Evidence map›Paper›PMID 42624994›Full record

ReviewNature biomedical engineering2026

Intracellular protein binders for imaging, control and future therapeutics.

Natalia V Barykina, Vladislav V Verkhusha

Abstract readReview
In one paragraph

Review in Nature biomedical engineering, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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.

Natalia V BarykinaDepartment of Genetics and Gruss-Lipper Biophotonics Center, Albert Einstein College of Medicine, New York, NY, USA.ORCID http://orcid.org/0000-0001-5835-8388
Vladislav V VerkhushaDepartment of Genetics and Gruss-Lipper Biophotonics Center, Albert Einstein College of Medicine, New York, NY, USA. vladislav.verkhusha@einsteinmed.edu.ORCID http://orcid.org/0000-0002-2083-8121

Funding

Near-Infrared Fluorescent Proteins, Biosensors and Optogenetic ToolsR35GM122567 · NIGMS · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI Vladislav Verkhusha · 2017 to 2026
$4.3M
Foundation for the National Institutes of Health (Foundation for the National Institutes of Health, Inc.) GM122567NIGMS NIH HHS R35 GM122567
6 · The paper itself

Abstract

Intracellular protein dysregulation underlies many cancers, neurodegenerative disorders and infectious diseases, yet a substantial fraction of the human proteome remains inaccessible to conventional small-molecule drugs or extracellular antibodies. Genetically encoded intracellular binders, including nanobodies, DARPins, affibodies and de novo-designed scaffolds, provide modular platforms for selective recognition, visualization and functional modulation of endogenous proteins in living cells. These binders can engage extended protein surfaces and conformational epitopes and are increasingly applied in preclinical models to inhibit oncogenic signalling, degrade pathogenic proteins, rewire cellular pathways and engineer programmable cell therapies. Here we outline the structural diversity, discovery strategies and design principles of intracellular binders and summarize their emerging applications in imaging, biosensing and targeted protein control. We further discuss recent advances in computationally assisted binder design and optimization. Finally, we examine key translational challenges, including cellular stability, delivery technologies and immunogenicity, that will shape the clinical development of intracellular binder-based therapeutics.

Identifiers

PMID42624994
PMCPMC13549425

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.