Evidence map›Paper›PMID 42327206›Full record

ArticlebioRxiv : the preprint server for biology2026

The NanoBridge system for targeted post-translational modification of challenging proteins.

Fangfang Shen, Olga D Merino-Chavez, Sheng-Yao Dai, Sebastian Alfonso, Laura M K Dassama

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 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

5 authors.

Fangfang ShenDepartment of Chemistry and Sarafan ChEM-H Institute, Stanford University, Stanford, California 94305, United States.
Olga D Merino-ChavezDepartment of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, California 94305, United States.
Sheng-Yao DaiDepartment of Radiology, Molecular Imaging Program at Stanford, Stanford University School of Medicine, Stanford, California 94305, United States.
Sebastian AlfonsoDepartment of Chemistry and Sarafan ChEM-H Institute, Stanford University, Stanford, California 94305, United States.
Laura M K DassamaDepartment of Chemistry and Sarafan ChEM-H Institute, Stanford University, Stanford, California 94305, United States.

Funding

Development of platforms for sorting, production, editing of beta cellsR01DK132900 · NIDDK · BROAD INSTITUTE, INC. · PI Amit Choudhary, Neal Krishna Devaraj · 2023 to 2026
$2.6M
Chemical tools for modulating the fetal hemoglobin inducer BCL11AR01HL173127 · NHLBI · STANFORD UNIVERSITY · PI Laura Dassama · 2024 to 2026
$1.2M
NHLBI NIH HHS R01 HL173127NIDDK NIH HHS R01 DK132900
6 · The paper itself

Abstract

The ability to edit posttranslational modifications (PTMs) of endogenous proteins within cells is essential for precisely delineating the biological roles of PTMs and for developing targeted therapeutics. While the paradigm of chemically induced proximity (CIP) has advanced this field by enabling the recruitment of PTM enzymes to the proximity of proteins of interest (POIs), CIP requires small-molecule binders that are difficult to obtain for proteins without well-defined binding pockets. In principle, the use of biomolecular ligands that target disordered proteins should overcome this limitation. In this work, we developed the NanoBridge as a modular and generalizable platform to enable PTM editing of challenging POIs in live cells. The NanoBridge employs biologic binders to transiently direct the small protein tag FKBP12

Identifiers

PMID42327206
PMCPMC13278106

What OpenQuestion holds

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LicenceCC BY
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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.