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
- living cells
- high resolution
- coronary artery disease
- early stage
- quantum dots
- mass spectrometry
- fluorescent probe
- ms ms
- cognitive decline
- newly diagnosed
- ejection fraction
- white matter
- squamous cell carcinoma
- pain management
- prognostic factors
- blood brain barrier
- resting state
- radiation therapy
- lymph node
- hydrogen peroxide
- binding protein
- climate change
- single molecule
- subarachnoid hemorrhage
- mild cognitive impairment
- high performance liquid chromatography