Evidence map›Paper›PMID 35058646›Full record

ReviewNature chemical biology2022

The evolution of synthetic receptor systems.

Janvie Manhas, Hailey I Edelstein, Joshua N Leonard, Leonardo Morsut

Abstract readReview
In one paragraph

Review in Nature chemical biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing 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

61 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. bioRxiv : the preprint server for biology · 2026
    Article
  6. Article
  7. Programming Next-Generation Synthetic Biosensors by Genetic Circuit Design.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Review
  20. Article

1 more citing papers are in PubMed but not listed here.

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

4 authors.

Janvie Manhas *Department of Biochemistry, All India Institute of Medical Sciences, New Delhi, India.ORCID http://orcid.org/0000-0001-6004-8004
Hailey I Edelstein *Department of Chemical and Biological Engineering, Northwestern University, Evanston, IL, USA.ORCID http://orcid.org/0000-0002-8077-5492
Joshua N LeonardDepartment of Chemical and Biological Engineering, Northwestern University, Evanston, IL, USA. j-leonard@northwestern.edu.ORCID http://orcid.org/0000-0003-4359-6126
Leonardo MorsutThe Eli and Edythe Broad CIRM Center, Department of Stem Cell Biology and Regenerative Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA. morsut@usc.edu.ORCID http://orcid.org/0000-0001-7049-3478

Funding

Design-driven engineering of robust mammalian sense-and-respond functions: from parts to programsR01EB026510 · NIBIB · NORTHWESTERN UNIVERSITY · PI Neda Bagheri, Joshua Nathaniel Leonard · 2018 to 2026
$3.7M
Synthetic development: dissection of morphogenetic programs via reconstructive and perturbative approachesR35GM138256 · NIGMS · UNIVERSITY OF SOUTHERN CALIFORNIA · PI MORSUT, LEONARDO · 2020 to 2024
$2.1M
Engineering Synthetic Receptor Systems That Can Detect Specific Cell-Cell Contact R00EB021030 · NIBIB · UNIVERSITY OF SOUTHERN CALIFORNIA · PI MORSUT, LEONARDO · 2017 to 2019
$716k
Engineering Synthetic Receptor Systems That Can Detect Specific Cell-Cell Contact SignalsK99EB021030 · NIBIB · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MORSUT, LEONARDO · 2015 to 2016
$195k
NIBIB NIH HHS K99 EB021030NIBIB NIH HHS R00 EB021030NIBIB NIH HHS R01 EB026510NIGMS NIH HHS R35 GM138256
6 · The paper itself

Abstract

Receptors enable cells to detect, process and respond to information about their environments. Over the past two decades, synthetic biologists have repurposed physical parts and concepts from natural receptors to engineer synthetic receptors. These technologies implement customized sense-and-respond programs that link a cell's interaction with extracellular and intracellular cues to user-defined responses. When combined with tools for information processing, these advances enable programming of sophisticated customized functions. In recent years, the library of synthetic receptors and their capabilities has substantially evolved-a term we employ here to mean systematic improvement and expansion. Here, we survey the existing mammalian synthetic biology toolkit of protein-based receptors and signal-processing components, highlighting efforts to evolve and integrate some of the foundational synthetic receptor systems. We then propose a generalized strategy for engineering and improving receptor systems to meet defined functional objectives called a 'metric-enabled approach for synthetic receptor engineering' (MEASRE).

Indexed as

Receptors, ArtificialAnimalsMammalsSynthetic BiologyReceptors, Artificial

Identifiers

PMID35058646
PMCPMC9041813

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.