4.7 Article

Natural and Designed Proteins Inspired by Extremotolerant Organisms Can Form Condensates and Attenuate Apoptosis in Human Cells

期刊

ACS SYNTHETIC BIOLOGY
卷 11, 期 3, 页码 1292-1302

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acssynbio.1c00572

关键词

stress tolerance; phase separation; intrinsically disordered proteins; apoptosis

资金

  1. NSF, DARPA
  2. Wyss Institute for Biologically Inspired Engineering
  3. Army Research Office [W911NF-19-2-0017]
  4. National Science Foundation [2010370]
  5. Harvard Medical School Department of Systems Biology
  6. Harvard Medical School Laboratory of Systems Pharmacology
  7. CZI Neurodegenerative Challenge Ben Barres Early Career Award [CZI2018-191853]
  8. HHMI Hanna Gray fellowship [GT11817]
  9. NCI [U54-CA225088]
  10. Direct For Biological Sciences
  11. Div Of Biological Infrastructure [2010370] Funding Source: National Science Foundation

向作者/读者索取更多资源

Many organisms have the ability to survive extreme conditions and recover to normal life, thanks in part to repetitive, amphipathic, and intrinsically disordered proteins. Through the evaluation of extremotolerance-associated proteins, it has been found that some of them can protect human cells from chemically induced apoptosis. Additionally, a region of the human ApoE protein has been identified with similarities to extremotolerance-associated proteins and also has the ability to protect against apoptosis.
Many organisms can survive extreme conditions and successfully recover to normal life. This extremotolerant behavior has been attributed in part to repetitive, amphipathic, and intrinsically disordered proteins that are upregulated in the protected state. Here, we assemble a library of approximately 300 naturally occurring and designed extremotolerance-associated proteins to assess their ability to protect human cells from chemically induced apoptosis. We show that several proteins from tardigrades, nematodes, and the Chinese giant salamander are apoptosis-protective. Notably, we identify a region of the human ApoE protein with similarity to extremotolerance-associated proteins that also protects against apoptosis. This region mirrors the phase separation behavior seen with such proteins, like the tardigrade protein CAHS2. Moreover, we identify a synthetic protein, DHR81, that shares this combination of elevated phase separation propensity and apoptosis protection. Finally, we demonstrate that driving protective proteins into the condensate state increases apoptosis protection, and highlights the ability of DHR81 condensates to sequester caspase-7. Taken together, this work draws a link between extremotolerance-associated proteins, condensate formation, and designing human cellular protection.

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