Engineered Bacteria with Genetic Circuits Accumulating Nanomagnets as MRI Contrast Agents.
Merve YavuzMustafa ÜtkürEbru Şahin KehribarEcrin YağızEmine Ülkü SarıtaşUrartu Özgür Şafak ŞekerPublished in: Small (Weinheim an der Bergstrasse, Germany) (2022)
The demand for highly efficient cancer diagnostic tools increases alongside the high cancer incidence nowadays. Moreover, there is an imperative need for novel cancer treatment therapies that lack the side effects of conventional treatment options. Developments in this aspect employ magnetic nanoparticles (MNPs) for biomedical applications due to their stability, biocompatibility, and magnetic properties. Certain organisms, including many bacteria, can synthesize magnetic nanocrystals, which help their spatial orientation and survival by sensing the earth's geomagnetic field. This work aims to convert Escherichia coli to accumulate magnetite, which can further be coupled with drug delivery modules. The authors design magnetite accumulating bacterial machines using genetic circuitries hiring Mms6 with iron-binding activity and essential in magnetite crystal formation. The work demonstrates that the combinatorial effect of Mms6 with ferroxidase, iron transporter protein, and material binding peptide enhances the paramagnetic behavior of the cells in magnetic resonance imaging (MRI) measurements. Cellular machines are also engineered to display Mms6 peptide on the cell surface via an autotransporter protein that shows augmented MRI performance. The findings are promising for endowing a probiotic bacterium, able to accumulate magnetite intracellularly or extracellularly, serving as a theranostics agent for cancer diagnostics via MRI scanning and hyperthermia treatment.
Keyphrases
- magnetic resonance imaging
- contrast enhanced
- papillary thyroid
- highly efficient
- drug delivery
- escherichia coli
- diffusion weighted imaging
- squamous cell
- cell surface
- magnetic nanoparticles
- computed tomography
- induced apoptosis
- binding protein
- lymph node metastasis
- molecularly imprinted
- gene expression
- small molecule
- squamous cell carcinoma
- high resolution
- mass spectrometry
- staphylococcus aureus
- cell death
- protein protein
- cell cycle arrest
- childhood cancer
- dna binding
- cystic fibrosis
- biofilm formation
- virtual reality