TY - JOUR

T1 - Cells have the ability to break and chemically modify GaP(As) nanowires

AU - Шмаков , Станислав

AU - Сосновицкая, Злата

AU - Махеева, Екатерина

AU - Аникина, Марина

AU - Кузнецов, Алексей

AU - Кондратьев, Валерий Михайлович

AU - Соломонов, Никита Александрович

AU - Бойцов, Виталий Михайлович

AU - Федоров, Владимир Викторович

AU - Мухин, Иван Сергеевич

AU - Букатин, Антон Сергеевич

AU - Большаков, Алексей Дмитриевич

AU - Резник, Родион Романович

PY - 2024/10/7

Y1 - 2024/10/7

N2 - Semiconductor nanowires are known for their unusual geometry, providing unique electronic and optical properties. Substrates with vertical nanowires have highly non-uniform surfaces, which are attractive in terms of the study of live cells that can interact and be labeled with the wires. Despite several previous works studying cells cultivated over nanowires, questions regarding cell rupture and interaction with the wires remain open. Here, we demonstrate that nanowires can not only penetrate the cell membrane, but even be broken by a cell and trapped inside it. Even after mechanical poration of the membrane manifested by the efficient transfection and delivery of a fluorescent protein encoding plasmid, the cells are found to be viable for 7 days of incubation. The endocytosed wires are then aligned along the nucleus periphery and ousted to pseudopodia with the formation of nanowire-rich fibrils as a result of complex intracellular processes. We demonstrate that endocytosis of the wires may lead to their chemical modification manifested by the red shift of the luminescence spectra. Analysis of the wires’ breakdown reveals that the cells can generate forces as high as several hundreds of nN. Using this work, we demonstrate several phenomena with the potential to be used in intriguing methods for intracellular visualization and the development of biointerfaces.

AB - Semiconductor nanowires are known for their unusual geometry, providing unique electronic and optical properties. Substrates with vertical nanowires have highly non-uniform surfaces, which are attractive in terms of the study of live cells that can interact and be labeled with the wires. Despite several previous works studying cells cultivated over nanowires, questions regarding cell rupture and interaction with the wires remain open. Here, we demonstrate that nanowires can not only penetrate the cell membrane, but even be broken by a cell and trapped inside it. Even after mechanical poration of the membrane manifested by the efficient transfection and delivery of a fluorescent protein encoding plasmid, the cells are found to be viable for 7 days of incubation. The endocytosed wires are then aligned along the nucleus periphery and ousted to pseudopodia with the formation of nanowire-rich fibrils as a result of complex intracellular processes. We demonstrate that endocytosis of the wires may lead to their chemical modification manifested by the red shift of the luminescence spectra. Analysis of the wires’ breakdown reveals that the cells can generate forces as high as several hundreds of nN. Using this work, we demonstrate several phenomena with the potential to be used in intriguing methods for intracellular visualization and the development of biointerfaces.

UR - https://www.mendeley.com/catalogue/65339cac-6713-3e21-bef1-d0f84d82b801/

U2 - 10.1039/d4nr02513j

DO - 10.1039/d4nr02513j

M3 - Article

JO - Nanoscale

JF - Nanoscale

SN - 2040-3364

ER -