Necrosis binding of Ac-Lys0(IRDye800CW)-Tyr3-octreotate: a consequence from cyanine-labeling of small molecules.
Marcus C M StroetBianca M DijkstraSebastiaan E DulferSchelto KruijffWilfred F A den DunnenFrank A E KruytRob J M GroenYann SeimbilleKranthi M PanthLaura MezzanotteClemens W G M LowikMarion de JongPublished in: EJNMMI research (2021)
This study shows that labeling peptides with cyanines can result in dead cell binding. This does not hamper the ultimate purpose of fluorescence-guided surgery, as necrotic tissue appears in most solid tumors. Hence, the necrosis binding can increase the overall tumor uptake. Moreover, necrotic tissue should be removed as much as possible: it cannot be salvaged, causes inflammation, and is tumorigenic. However, when performing binding experiments to cells with disrupted membrane integrity, which is routinely done with nuclear probes, this dead cell-binding can resemble non-specific binding. This study will benefit the development of fluorescent contrast agents.
Keyphrases
- dna binding
- binding protein
- minimally invasive
- stem cells
- oxidative stress
- cell therapy
- single molecule
- magnetic resonance
- small molecule
- computed tomography
- magnetic resonance imaging
- coronary artery bypass
- bone marrow
- quantum dots
- acute coronary syndrome
- endoplasmic reticulum stress
- transcription factor
- functional connectivity