Photoactive surfactant semiconductors characterized by a dissociative identity disorder integrated into the membranes of living cells as trojan horses for on-demand and spatial regulation of oxidative stress.

Publikation: Arbeitspapier/PreprintArbeitspapier/Diskussionspapier

Autoren

  • Marian Jaschke
  • Masina Plenge
  • Marius Kunkel
  • Tina Lehrich
  • Julia Schmidt
  • Kilian Stöckemann
  • Dag Heinemann
  • Stephan Siroky
  • Anaclet Ngezahay
  • Sebastian Polarz
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Details

OriginalspracheEnglisch
Seitenumfang7
PublikationsstatusVeröffentlicht - 16 Aug. 2022

Abstract

Oxidative stress is a cause for numerous diseases and aging processes. Thus, one is keen to tune the level of intracellular stress and to learn from that, and an unusual approach is presented here. The methodology involves multifunctional surfactants. Although their molecular design is non-biological, a fullerenol head group attached covalently to -conjugated dyes, the surfactants possess superior biocompatibility. Using the intrinsic fluorescence signal as a probe it is proven, the amphiphiles become incorporated into the membranes of Caco-2 cells. There, they are able to exhibit additional functions. The compound reduces cellular stress in dark reaction pathways. The antagonistic property is activated under irradiation, the photocatalytic production of ROS, resulting in cell damage and finally to apoptosis. The feature is activated even by NIR-light via a two-photon process. The properties as molecular semiconductors leads to a trojan horse situation and allows programming the spatial distribution of cytotoxicity.

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title = "Photoactive surfactant semiconductors characterized by a dissociative identity disorder integrated into the membranes of living cells as trojan horses for on-demand and spatial regulation of oxidative stress.",
abstract = "Oxidative stress is a cause for numerous diseases and aging processes. Thus, one is keen to tune the level of intracellular stress and to learn from that, and an unusual approach is presented here. The methodology involves multifunctional surfactants. Although their molecular design is non-biological, a fullerenol head group attached covalently to -conjugated dyes, the surfactants possess superior biocompatibility. Using the intrinsic fluorescence signal as a probe it is proven, the amphiphiles become incorporated into the membranes of Caco-2 cells. There, they are able to exhibit additional functions. The compound reduces cellular stress in dark reaction pathways. The antagonistic property is activated under irradiation, the photocatalytic production of ROS, resulting in cell damage and finally to apoptosis. The feature is activated even by NIR-light via a two-photon process. The properties as molecular semiconductors leads to a trojan horse situation and allows programming the spatial distribution of cytotoxicity. ",
author = "Marian Jaschke and Masina Plenge and Marius Kunkel and Tina Lehrich and Julia Schmidt and Kilian St{\"o}ckemann and Dag Heinemann and Stephan Siroky and Anaclet Ngezahay and Sebastian Polarz",
note = "Acknowledgment: We thank Helma Feierabend for technical support.",
year = "2022",
month = aug,
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doi = "10.26434/chemrxiv-2022-587qb",
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TY - UNPB

T1 - Photoactive surfactant semiconductors characterized by a dissociative identity disorder integrated into the membranes of living cells as trojan horses for on-demand and spatial regulation of oxidative stress.

AU - Jaschke, Marian

AU - Plenge, Masina

AU - Kunkel, Marius

AU - Lehrich, Tina

AU - Schmidt, Julia

AU - Stöckemann, Kilian

AU - Heinemann, Dag

AU - Siroky, Stephan

AU - Ngezahay, Anaclet

AU - Polarz, Sebastian

N1 - Acknowledgment: We thank Helma Feierabend for technical support.

PY - 2022/8/16

Y1 - 2022/8/16

N2 - Oxidative stress is a cause for numerous diseases and aging processes. Thus, one is keen to tune the level of intracellular stress and to learn from that, and an unusual approach is presented here. The methodology involves multifunctional surfactants. Although their molecular design is non-biological, a fullerenol head group attached covalently to -conjugated dyes, the surfactants possess superior biocompatibility. Using the intrinsic fluorescence signal as a probe it is proven, the amphiphiles become incorporated into the membranes of Caco-2 cells. There, they are able to exhibit additional functions. The compound reduces cellular stress in dark reaction pathways. The antagonistic property is activated under irradiation, the photocatalytic production of ROS, resulting in cell damage and finally to apoptosis. The feature is activated even by NIR-light via a two-photon process. The properties as molecular semiconductors leads to a trojan horse situation and allows programming the spatial distribution of cytotoxicity.

AB - Oxidative stress is a cause for numerous diseases and aging processes. Thus, one is keen to tune the level of intracellular stress and to learn from that, and an unusual approach is presented here. The methodology involves multifunctional surfactants. Although their molecular design is non-biological, a fullerenol head group attached covalently to -conjugated dyes, the surfactants possess superior biocompatibility. Using the intrinsic fluorescence signal as a probe it is proven, the amphiphiles become incorporated into the membranes of Caco-2 cells. There, they are able to exhibit additional functions. The compound reduces cellular stress in dark reaction pathways. The antagonistic property is activated under irradiation, the photocatalytic production of ROS, resulting in cell damage and finally to apoptosis. The feature is activated even by NIR-light via a two-photon process. The properties as molecular semiconductors leads to a trojan horse situation and allows programming the spatial distribution of cytotoxicity.

U2 - 10.26434/chemrxiv-2022-587qb

DO - 10.26434/chemrxiv-2022-587qb

M3 - Working paper/Discussion paper

BT - Photoactive surfactant semiconductors characterized by a dissociative identity disorder integrated into the membranes of living cells as trojan horses for on-demand and spatial regulation of oxidative stress.

ER -

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