4.4 Review

Intracellular Thermometry at the Micro-/Nanoscale and its Potential Application to Study Protein Aggregation Related to Neurodegenerative Diseases

Journal

CHEMBIOCHEM
Volume 22, Issue 9, Pages 1546-1558

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cbic.202000765

Keywords

amyloid-beta peptides; fluorescent probes; nanoparticles

Funding

  1. Cambridge Trust
  2. Wolfson College
  3. Wellcome Trust [065807/Z/01/Z, 203249/Z/16/Z]
  4. UK Medical Research Council (MRC) [MR/K02292X/1]
  5. Alzheimer Research UK (ARUK) [ARUK-PG013-14]
  6. Michael J Fox Foundation [16238]
  7. Infinitus China Ltd.
  8. BBSRC [BB/H023917/1] Funding Source: UKRI
  9. MRC [MR/K02292X/1, G0902243] Funding Source: UKRI

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Temperature is a crucial factor influencing biological processes in living cells, and intracellular temperature mapping can provide valuable insights into thermodynamic properties and cellular behavior. This review focuses on various thermometry systems, particularly those utilizing fluorescence-based techniques, discussing findings from intracellular measurements and highlighting discrepancies in current thermodynamic understanding related to mitochondrial thermogenesis and nuclear-cytoplasmic temperature differences. Additionally, intracellular thermometry is proposed as a tool for quantifying the energy flow and costs associated with A beta 42 aggregation in Alzheimer's disease.
Temperature is a fundamental physical parameter that influences biological processes in living cells. Hence, intracellular temperature mapping can be used to derive useful information reflective of thermodynamic properties and cellular behaviour. Herein, existing publications on different thermometry systems, focusing on those that employ fluorescence-based techniques, are reviewed. From developments based on fluorescent proteins and inorganic molecules to metal nanoclusters and fluorescent polymers, the general findings of intracellular measurements from different research groups are discussed. Furthermore, the contradiction of mitochondrial thermogenesis and nuclear-cytoplasmic temperature differences to current thermodynamic understanding are highlighted. Lastly, intracellular thermometry is proposed as a tool to quantify the energy flow and cost associated with amyloid-beta 42 (A beta 42) aggregation, a hallmark of Alzheimer's disease.

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