4.8 Article

Directed Evolution of a Selective and Sensitive Serotonin Sensor via Machine Learning

Journal

CELL
Volume 183, Issue 7, Pages 1986-+

Publisher

CELL PRESS
DOI: 10.1016/j.cell.2020.11.040

Keywords

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Funding

  1. National Institute of General Medical Sciences from the NIH [P30-GM124165]
  2. NIH-ORIP HEI grant [S10-RR029205]
  3. DOE Office of Science [DE-AC02-06CH11357]
  4. NIH [U01NS090604, U01NS013522, DP2MH107056, BRAIN RF1MH117069, R01AA019454, P60AA011605, U24AA025475, 5T32NS007431-20]
  5. Mistletoe Foundation Research Fellowship
  6. ARCS Scholarship
  7. Howard Hughes Medical Institute
  8. Heritage Medical Research Institute
  9. Center for Molecular and Cellular Neuroscience of the Chen Institute
  10. Beckman Institute for CLARITY, Optogenetics and Vector Engineering Research
  11. NIAAA [ZIA-AA000421]
  12. NINDS [ZIA-AA000421]
  13. Innovation Award from NIH-DDIR

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Serotonin plays a central role in cognition and is the target of most pharmaceuticals for psychiatric disorders. Existing drugs have limited efficacy; creation of improved versions will require better understanding of serotonergic circuitry, which has been hampered by our inability to monitor serotonin release and transport with high spatial and temporal resolution, We developed and applied a binding-pocket redesign strategy, guided by machine learning, to create a high-performance, soluble, fluorescent serotonin sensor (iSeroSnFR), enabling optical detection of millisecond-scale serotonin transients. We demonstrate that iSeroSnFR can be used to detect serotonin release in freely behaving mice during fear conditioning, social interaction, and sleep/wake transitions, We also developed a robust assay of serotonin transporter function and modulation by drugs. We expect that both machine-learning-guided binding-pocket redesign and iSeroSnFR will have broad utility for the development of other sensors and in vitro and in vivo serotonin detection, respectively.

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