Evidence map›Paper›PMID 39999860›Full record

ReviewAnnual review of analytical chemistry (Palo Alto, Calif.)2025

Protein Engineering for Spatiotemporally Resolved Cellular Monitoring.

Guanwei Zhou, Wenjing Wang

Abstract readReview
In one paragraph

Review in Annual review of analytical chemistry (Palo Alto, Calif.), 2025. 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.

Guanwei ZhouLife Sciences Institute and Program in Chemical Biology, University of Michigan, Ann Arbor, Michigan, USA; email: guzhou@umich.edu, wenjwang@umich.edu.
Wenjing WangLife Sciences Institute and Program in Chemical Biology, University of Michigan, Ann Arbor, Michigan, USA; email: guzhou@umich.edu, wenjwang@umich.edu.

Funding

New classes of optogenetic and chemogenetic tools with a feedback controlDP2MH132939 · NIMH · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WANG, WENJING · 2022 to 2025
$2.3M
Design of genetically encoded sensors for detecting endogenous opioid peptidesR01DA053200 · NIDA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Wenjing Wang · 2022 to 2026
$1.7M
Design and characterization of Nanobodies to dementia-related α-synuclein strains in Parkinson’s diseaseR21AG072009 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WANG, WENJING · 2021 to 2021
$454k
NIA NIH HHS R21 AG072009NIDA NIH HHS R01 DA053200NIMH NIH HHS DP2 MH132939
6 · The paper itself

Abstract

Protein engineering has been extensively applied to the development of genetically encoded reporters for spatiotemporally resolved monitoring of dynamic biochemical activity across cellular compartments in living cells. Genetically encoded reporters facilitate the visualization and recording of cellular processes, including transmission of signaling molecules, protease activity, and protein-protein interactions. In this review, we describe and assess common reporter motifs and protein engineering strategies for designing genetically encoded reporters. We also discuss essential parameters for evaluating genetically encoded reporters, along with future protein engineering opportunities in this field.

Indexed as

Protein EngineeringAnimalsGenes, ReporterHumansgenetically encoded reportersprotease activityprotein engineeringprotein–protein interactionssignaling moleculesspatiotemporal resolution

Identifiers

PMID39999860
PMCPMC12081197

What OpenQuestion holds

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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.