4.7 Article

Activatable Photosensitizer for Targeted Ablation of lacZ-Positive Cells with Single-Cell Resolution

Journal

ACS CENTRAL SCIENCE
Volume 5, Issue 10, Pages 1676-1681

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acscentsci.9b00678

Keywords

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Funding

  1. AMED [JP19gm0710008, JP17gm0610004, JP19gm5010001]
  2. JST/PRESTO [JPMJPR14F8]
  3. MEXT/JSPS KAKENHI [JP16H02606, JP26111012, JP19H05632, JP15H05951, JP19H02826, JP19K22242, 16H06385]
  4. JSPS Core-to-Core Program
  5. Astellas Foundation for Research on Metabolic Disorders
  6. Japan Foundation for Applied Enzymology
  7. Japan Society for the Promotion of Science
  8. Grants-in-Aid for Scientific Research [16H06385] Funding Source: KAKEN

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To achieve highly selective ablation of lacZ-positive cells in a biological milieu in vivo, we developed an activatable photosensitizer, SPiDER-killer-beta Gal, targeted to beta-galactosidase encoded by the lacZ reporter gene. Hydrolysis of SPiDER-killer-beta Gal by beta-galactosidase simultaneously activates both its photosensitizing ability and its reactivity to nucleophiles, so that the phototoxic products generated by light irradiation are trapped inside the lacZ-positive cells. The combination of SPiDER-killer-beta Gal and light irradiation specifically killed lacZ-positive cells in coculture with cells without lacZ expression. Furthermore, beta-galactosidase-expressing cells in the posterior region of cultured Drosophila wing discs and in pupal notum of live Drosophila pupae were selectively killed with single-cell resolution. This photosensitizer should be useful for specific ablation of targeted cells in living organisms, for example, to investigate cellular functions in complex networks.

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