Evidence map›Paper›PMID 36055250›Full record

ArticleCell2022

helixCAM: A platform for programmable cellular assembly in bacteria and human cells.

George Chao, Timothy M Wannier, Clair Gutierrez, Nathaniel C Borders, Evan Appleton, Anjali Chadha, Tina Lebar, George M Church

Open access · greenAbstract read
In one paragraph

Article in Cell, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.3field-weighted citation impact, top 7% of its field
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

21 citing papers in PubMed, 43 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Protein engineering: status report.Protein engineering, design & selection : PEDS · 2026
    Review
  6. Programming cellular condensates for living materials using an intrinsically disordered protein display platform.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Cell-Membrane-Anchored DNA Nanoplatform for Programming Cellular Interactions.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Designer cell therapy for tissue regeneration.Inflammation and regeneration · 2024
    Review
  20. Article
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

8 authors at 2 institutions in 1 country.

George ChaoGenetics Department, Harvard Medical School, Boston, MA 02115, USA. Electronic address: gchao@hms.harvard.edu.
Timothy M WannierGenetics Department, Harvard Medical School, Boston, MA 02115, USA.
Clair GutierrezDepartment of Chemistry, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Nathaniel C BordersGenetics Department, Harvard Medical School, Boston, MA 02115, USA.
Evan AppletonGenetics Department, Harvard Medical School, Boston, MA 02115, USA.
Anjali ChadhaDepartment of Bioengineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Tina LebarWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA 02115, USA.
George M ChurchGenetics Department, Harvard Medical School, Boston, MA 02115, USA; Wyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA 02115, USA. Electronic address: gchurch@genetics.med.harvard.edu.
Harvard University · USMassachusetts Institute of Technology · US

Funding

Center for Genomically Engineered OrgansRM1HG008525 · NHGRI · HARVARD MEDICAL SCHOOL · PI CHURCH, GEORGE M · 2015 to 2019
$10.2M
NHGRI NIH HHS RM1 HG008525
6 · The paper itself

Abstract

Interactions between cells are indispensable for signaling and creating structure. The ability to direct precise cell-cell interactions would be powerful for engineering tissues, understanding signaling pathways, and directing immune cell targeting. In humans, intercellular interactions are mediated by cell adhesion molecules (CAMs). However, endogenous CAMs are natively expressed by many cells and tend to have cross-reactivity, making them unsuitable for programming specific interactions. Here, we showcase "helixCAM," a platform for engineering synthetic CAMs by presenting coiled-coil peptides on the cell surface. helixCAMs were able to create specific cell-cell interactions and direct patterned aggregate formation in bacteria and human cells. Based on coiled-coil interaction principles, we built a set of rationally designed helixCAM libraries, which led to the discovery of additional high-performance helixCAM pairs. We applied this helixCAM toolkit for various multicellular engineering applications, such as spherical layering, adherent cell targeting, and surface patterning.

Indexed as

BacteriaPeptidesHumansPeptidescell aggregationcell interactioncell patterningcell targetingimage processingmammalian synthetic biologymembrane proteinprotein engineeringrational designtissue engineering

Identifiers

PMID36055250
PMCPMC9481732
OpenAlexW4294012299

What OpenQuestion holds

Textmetadata
LicenceTDM
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.