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Bacterial Phytochrome as a Scaffold for Engineering of Receptor Tyrosine Kinases Controlled with Near-Infrared Light

  1. Author:
    Leopold, Anna
    Pletnev,Sergei
    Verkhusha, Vladislav V.
  2. Author Address

    Univ Helsinki, Fac Med, Med, Helsinki 00290, Finland.Leidos Biomed Res Inc, Macromol Crystallog Lab, NCI, Basic Sci Program, Argonne, IL 60439 USA.Albert Einstein Coll Med, Dept Anat & Struct Biol, Bronx, NY 10461 USA.Albert Einstein Coll Med, Gruss Lipper Biophoton Ctr, Bronx, NY 10461 USA.
    1. Year: 2020
    2. Date: JUN 12
  1. Journal: JOURNAL OF MOLECULAR BIOLOGY
  2. ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD,
    1. 432
    2. 13
    3. Pages: 3749-3760
  3. Type of Article: Article
  4. ISSN: 0022-2836
  1. Abstract:

    Optically controlled receptor tyrosine kinases (opto-RTKs) allow regulation of RTK signaling using light. Until recently, the majority of opto-RTKs were activated with blue-green light. Fusing a photosensory core module of Deinococcus radiodurans bacterial phytochrome (DrBphP-PCM) to the kinase domains of neurotrophin receptors resulted in opto-RTKs controlled with light above 650 nm. To expand this engineering approach to RTKs of other families, here we combined the DrBpP-PCM with the cytoplasmic domains of EGFR and FGFR1. The resultant Dr-EGFR and Dr-FGFR1 opto-RTKs are rapidly activated with near-infrared and inactivated with far-red light. The opto-RTKs efficiently trigger ERK1/2, PI3K/Akt, and PLC gamma signaling. Absence of spectral crosstalk between the opto-RTKs and green fluorescent protein-based biosensors enables simultaneous Dr-FGFR1 activation and detection of calcium transients. Action mechanism of the DrBphP-PCM-based opto-RTKs is considered using the available RTK structures. DrBphP-PCM represents a versatile scaffold for engineering of opto-RTKs that are reversibly regulated with far-red and near-infrared light. (C) 2020 Elsevier Ltd. All rights reserved.

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External Sources

  1. DOI: 10.1016/j.jmb.2020.04.005
  2. WOS: 000541931500002

Library Notes

  1. Fiscal Year: FY2019-2020
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