4.3 Article

Inventing a co-axial atomic resolution patch clamp to study a single resonating protein complex and ultra-low power communication deep inside a living neuron cell

期刊

JOURNAL OF INTEGRATIVE NEUROSCIENCE
卷 15, 期 4, 页码 403-433

出版社

IMR PRESS
DOI: 10.1142/S0219635216500321

关键词

Neuron; protein; resonance; patch clamp; electromagnetic property

资金

  1. Asian office of Aerospace R&D (AOARD) a part of United States Air Force (USAF) [FA2386-16-1-0003]

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To read the signals of single molecules in vitro on a surface, or inside a living cell or organ, we introduce a coaxial atom tip (coat) and a coaxial atomic patch clamp (COAPAP). The metalinsulator-metal cavity of these probes extends to the atomic scale (0.1 nm), it eliminates the cellular or environmental noise with a S/N ratio 10(5). Five ac signals are simultaneously applied during a measurement by COAT and COAPAP to shield a true signal under environmental noise in five unique ways. The electromagnetic drive in the triaxial atomic tips is specifically designed to sense anharmonic vibrational and transmission signals for any system between 0.1 nm and 50 nm where the smallest nanopatch clamp cannot reach. COAT and COAPAP reliably pick up the atomic scale vibrations under the extreme noise of a living cell. Each protein's distinct electromagnetic, mechanical, electrical and ionic vibrational signature studied in vitro in a protected environment is found to match with the ones studied inside a live neuron. Thus, we could confirm that by using our probe blindly we could hold on to a single molecule or its complex in the invisible domain of a living cell. Our decade long investigations on perfecting the tools to measure bio-resonance of all forms and simultaneously in all frequency domains are summarized. It shows that the ratio of emission to absorption resonance frequencies of a biomaterial is around pi, only a few in the entire em spectrum are active that regulates all other resonances, like mechanical, ionic, etc.

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