A probe for NIR-II imaging and multimodal analysis of early Alzheimer's disease by targeting CTGF.
Cao LuCong MengYuying LiJinling YuanXiaojun RenLiang GaoDongdong SuKai CaoMeng-Chao CuiQing YuanXueyun GaoPublished in: Nature communications (2024)
To date, earlier diagnosis of Alzheimer's disease (AD) is still challenging. Recent studies revealed the elevated expression of connective tissue growth factor (CTGF) in AD brain is an upstream regulator of amyloid-beta (Aβ) plaque, thus CTGF could be an earlier diagnostic biomarker of AD than Aβ plaque. Herein, we develop a peptide-coated gold nanocluster that specifically targets CTGF with high affinity (KD ~ 21.9 nM). The probe can well penetrate the blood-brain-barrier (BBB) of APP/PS1 transgenic mice at early-stage (earlier than 3-month-old) in vivo, allowing non-invasive NIR-II imaging of CTGF when there is no appearance of Aβ plaque deposition. Notably, this probe can also be applied to measuring CTGF on postmortem brain sections by multimodal analysis, including fluorescence imaging, peroxidase-like chromogenic imaging, and ICP-MS quantitation, which enables distinguishment between the brains of AD patients and healthy people. This probe possesses great potential for precise diagnosis of earlier AD before Aβ plaque formation.
Keyphrases
- fluorescence imaging
- photodynamic therapy
- growth factor
- high resolution
- living cells
- coronary artery disease
- early stage
- quantum dots
- end stage renal disease
- mass spectrometry
- fluorescent probe
- ms ms
- cognitive decline
- chronic kidney disease
- multiple sclerosis
- newly diagnosed
- white matter
- ejection fraction
- resting state
- radiation therapy
- liquid chromatography tandem mass spectrometry
- squamous cell carcinoma
- transcription factor
- peritoneal dialysis
- lymph node
- high performance liquid chromatography
- patient reported outcomes
- drug release
- mild cognitive impairment
- binding protein
- rectal cancer
- tandem mass spectrometry