4.8 Article

Comprehensive Dual- and Triple-Feature Intersectional Single-Vector Delivery of Diverse Functional Payloads to Cells of Behaving Mammals

期刊

NEURON
卷 107, 期 5, 页码 836-+

出版社

CELL PRESS
DOI: 10.1016/j.neuron.2020.06.003

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资金

  1. NSF
  2. Stanford Bio-X
  3. Kwanjeong Fellowship
  4. NIMH
  5. NIH
  6. DARPA
  7. Gatsby Foundation
  8. NOMIS Foundation
  9. Wiegers Foundation
  10. Tarlton Foundation
  11. Fresenius Foundation
  12. Stanford Psychiatry

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The resolution and dimensionality with which biologists can characterize cell types have expanded dramatically in recent years, and intersectional consideration of such features (e.g., multiple gene expression and anatomical parameters) is increasingly understood to be essential. At the same time, genetically targeted technology for writing in and reading out activity patterns for cells in living organisms has enabled causal investigation in physiology and behavior; however, cell-type-specific delivery of these tools (including microbial opsins for optogenetics and genetically encoded Ca2+ indicators) has thus far fallen short of versatile targeting to cells jointly defined by many individually selected features. Here, we develop a comprehensive intersectional targeting toolbox including 39 novel vectors for joint-feature-targeted delivery of 13 molecular payloads (including opsins, indicators, and fluorophores), systematic approaches for development and optimization of new intersectional tools, hardware for in vivo monitoring of expression dynamics, and the first versatile single-virus tools (Triplesect) that enable targeting of triply defined cell types.

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