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Multifaceted Regulation of Potassium-Ion Channels by Graphene Quantum Dots.
Gu, Zonglin; Baggetta, Austin M; Chong, Yu; Plant, Leigh D; Meng, Xuan-Yu; Zhou, Ruhong.
Afiliação
  • Gu Z; Institute of Quantitative Biology and Medicine, SRMP and RAD-X, State Key Laboratory of Radiation Medicine and Protection, Soochow University, Suzhou 215123, China.
  • Baggetta AM; Institute of Quantitative Biology, Shanghai Institute for Advanced Study, Department of Physics, Zhejiang University, Hangzhou 310027, China.
  • Chong Y; Department of Pharmaceutical Sciences, Bouvé College of Health Sciences, Northeastern University, 360 Huntington Avenue, Boston, Massachusetts 02115, United States.
  • Plant LD; Institute of Quantitative Biology and Medicine, SRMP and RAD-X, State Key Laboratory of Radiation Medicine and Protection, Soochow University, Suzhou 215123, China.
  • Meng XY; Department of Pharmaceutical Sciences, Bouvé College of Health Sciences, Northeastern University, 360 Huntington Avenue, Boston, Massachusetts 02115, United States.
  • Zhou R; Institute of Quantitative Biology and Medicine, SRMP and RAD-X, State Key Laboratory of Radiation Medicine and Protection, Soochow University, Suzhou 215123, China.
ACS Appl Mater Interfaces ; 13(24): 27784-27795, 2021 Jun 23.
Article em En | MEDLINE | ID: mdl-34126740
Graphene quantum dots (GQDs) are emerging as a versatile nanomaterial with numerous proposed biomedical applications. Despite the explosion in potential applications, the molecular interactions between GQDs and complex biomolecular systems, including potassium-ion (K+) channels, remain largely unknown. Here, we use molecular dynamics (MD) simulations and electrophysiology to study the interactions between GQDs and three representative K+ channels, which participate in a variety of physiological processes and are closely related to many disease states. Using MD simulations, we observed that GQDs adopt distinct contact poses with each of the three structurally distinct K+ channels. Our electrophysiological characterization of the effects of GQDs on channel currents revealed that GQDs interact with the extracellular voltage-sensing domain (VSD) of a Kv1.2 channel, augmenting current by left-shifting the voltage dependence of channel activation. In contrast, GQDs form a "lid" cluster over the extracellular mouth of inward rectifier Kir3.2, blocking the channel pore and decreasing the current in a concentration-dependent manner. Meanwhile, GQDs accumulate on the extracellular "cap domain" of K2P2 channels and have no apparent impact on the K+ flux through the channel. These results reveal a surprising multifaceted regulation of K+ channels by GQDs, which might help de novo design of nanomaterial-based channel probe openers/inhibitors that can be used to further discern channel function.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Canais de Potássio de Domínios Poros em Tandem / Pontos Quânticos / Canais de Potássio Corretores do Fluxo de Internalização Acoplados a Proteínas G / Canal de Potássio Kv1.2 / Grafite Idioma: En Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Canais de Potássio de Domínios Poros em Tandem / Pontos Quânticos / Canais de Potássio Corretores do Fluxo de Internalização Acoplados a Proteínas G / Canal de Potássio Kv1.2 / Grafite Idioma: En Ano de publicação: 2021 Tipo de documento: Article País de afiliação: China