Scalable ultrasmall three-dimensional nanowire transistor probes for intracellular recording

被引:134
作者
Zhao, Yunlong [1 ,2 ]
You, Siheng Sean [1 ]
Zhang, Anqi [1 ]
Lee, Jae-Hyun [1 ,3 ]
Huang, Jinlin [1 ]
Lieber, Charles M. [1 ,4 ,5 ]
机构
[1] Harvard Univ, Dept Chem & Chem Biol, Cambridge, MA 02138 USA
[2] Univ Surrey, Adv Technol Inst, Guildford, Surrey, England
[3] Yonsei Univ, Yonsei IBS Inst, IBS, Ctr Nanomed, Seoul, South Korea
[4] Harvard Univ, Ctr Brain Sci, Cambridge, MA 02138 USA
[5] Harvard Univ, John A Paulson Sch Engn & Appl Sci, Cambridge, MA 02138 USA
关键词
MEMBRANE CURVATURE; ACTION-POTENTIALS; CELLS; NEUROSCIENCE; MECHANISMS; NEURONS; DEVICES; ARRAY;
D O I
10.1038/s41565-019-0478-y
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
New tools for intracellular electrophysiology that push the limits of spatiotemporal resolution while reducing invasiveness could provide a deeper understanding of electrogenic cells and their networks in tissues, and push progress towards human-machine interfaces. Although significant advances have been made in developing nanodevices for intracellular probes, current approaches exhibit a trade-off between device scalability and recording amplitude. We address this challenge by combining deterministic shape-controlled nanowire transfer with spatially defined semiconductor-to-metal transformation to realize scalable nanowire field-effect transistor probe arrays with controllable tip geometry and sensor size, which enable recording of up to 100 mV intracellular action potentials from primary neurons. Systematic studies on neurons and cardiomyocytes show that controlling device curvature and sensor size is critical for achieving high-amplitude intracellular recordings. In addition, this device design allows for multiplexed recording from single cells and cell networks and could enable future investigations of dynamics in the brain and other tissues.
引用
收藏
页码:783 / +
页数:10
相关论文
共 43 条
  • [1] Plasma Membrane and Actin Cytoskeleton as Synergistic Barriers to Nanowire Cell Penetration
    Aalipour, Amin
    Xu, Alexander M.
    Leal-Ortiz, Sergio
    Garner, Craig C.
    Melosh, Nicholas A.
    [J]. LANGMUIR, 2014, 30 (41) : 12362 - 12367
  • [2] Optimizing Nanoelectrode Arrays for Scalable Intracellular Electrophysiology
    Abbott, Jeffrey
    Ye, Tianyang
    Ham, Donhee
    Park, Hongkun
    [J]. ACCOUNTS OF CHEMICAL RESEARCH, 2018, 51 (03) : 600 - 608
  • [3] Abbott J, 2017, NAT NANOTECHNOL, V12, P460, DOI [10.1038/nnano.2017.3, 10.1038/NNANO.2017.3]
  • [4] [Anonymous], 2021, INTRO SOLID STATE PH
  • [5] [Anonymous], 2018, CARD US MAN
  • [6] Burridge PW, 2014, NAT METHODS, V11, P855, DOI [10.1038/nmeth.2999, 10.1038/NMETH.2999]
  • [7] Neural recording and modulation technologies
    Chen, Ritchie
    Canales, Andres
    Anikeeva, Polina
    [J]. NATURE REVIEWS MATERIALS, 2017, 2 (02):
  • [8] Functional organization of excitatory synaptic strength in primary visual cortex
    Cossell, Lee
    Iacaruso, Maria Florencia
    Muir, Dylan R.
    Houlton, Rachael
    Sader, Elie N.
    Ko, Ho
    Hofer, Sonja B.
    Mrsic-Flogel, Thomas D.
    [J]. NATURE, 2015, 518 (7539) : 399 - 403
  • [9] Molecular mechanisms of mechanotransduction in mammalian sensory neurons
    Delmas, Patrick
    Hao, Jizhe
    Rodat-Despoix, Lise
    [J]. NATURE REVIEWS NEUROSCIENCE, 2011, 12 (03) : 139 - 153
  • [10] Cholesterol metabolism in the central nervous system during early development and in the mature animal
    Dietschy, JM
    Turley, SD
    [J]. JOURNAL OF LIPID RESEARCH, 2004, 45 (08) : 1375 - 1397