Abstract

Life may be expressed as the flow of electrons, protons, and other ions, resulting in large potential difference. It is also highly photo-sensitive, as a large proportion of the redox capable molecules it relies on are chromophoric. It is thus suggestive that a key organelle in eukaryotes, the mitochondrion, constantly adapt their morphology as part of the homeostatic process. Studying unstained in vivo nano-scale structure in live cells is technically very challenging. One option is to study a central electron carrier in metabolism, reduced nicotinamide adenine dinucleotide (NADH), which is fluorescent and mostly located within mitochondria. Using one and two-photon absorption (340–360 nm and 730 nm, respectively), fluorescence lifetime imaging and anisotropy spectroscopy of NADH in solution and in live cells, we show that mitochondria do indeed appear to be aligned and exhibit high anisotropy (asymmetric directionality). Aqueous solution of NADH showed an anisotropy of ~ 0.20 compared to fluorescein or coumarin of < 0.1 and 0.04 in water respectively and as expected for small organic molecules. The anisotropy of NADH also increased further to 0.30 in the presence of proteins and 0.42 in glycerol (restricted environment) following two-photon excitation, suggesting more ordered structures. Two-photon NADH fluorescence imaging of Michigan Cancer Foundation-7 (MCF7) also showed strong anisotropy of 0.25 to 0.45. NADH has a quantum yield of fluorescence of 2% compared to more than 40% for photoionisation (electron generation), when exposed to light at 360 nm and below. The consequence of such highly ordered and directional NADH patterns with respect to electron ejection upon ultra-violet (UV) excitation could be very informative—especially in relation to ascertaining the extent of quantum effects in biology, including electron and photonic cascade, communication and modulation of effects such as spin and tunnelling.

Details

Title
The use of NADH anisotropy to investigate mitochondrial cristae alignment
Author
Smith, Holly. E. 1 ; Mackenzie, Alasdair M. 1 ; Seddon, Chloe 2 ; Mould, Rhys 3 ; Kalampouka, Ifi 3 ; Malakar, Partha 1 ; Needham, Sarah R. 1 ; Beis, Konstantinos 2   VIAFID ORCID Logo  ; Bell, Jimmy D. 3 ; Nunn, Alistair 3 ; Botchway, Stanley W. 1   VIAFID ORCID Logo 

 Rutherford Appleton Laboratory, UKRI, STFC, Central Laser Facility, Oxfordshire, UK (GRID:grid.76978.37) (ISNI:0000 0001 2296 6998) 
 Imperial College London, Department of Life Sciences, London, UK (GRID:grid.7445.2) (ISNI:0000 0001 2113 8111); Research Complex at Harwell, Rutherford Appleton Laboratory, Didcot, Oxfordshire, UK (GRID:grid.465239.f) 
 University of Westminster, School of Life Sciences, Research Centre for Optimal Health, London, UK (GRID:grid.12896.34) (ISNI:0000 0000 9046 8598) 
Pages
5980
Publication year
2024
Publication date
2024
Publisher
Nature Publishing Group
e-ISSN
20452322
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2955982156
Copyright
© The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.