Cited by 41Alzheimer's disease research and treatmentsDementia and Cognitive Impairment ResearchMedical Imaging Techniques and Applications

Characterization of MK6240, a tau PET tracer, in autopsy brain tissue from Alzheimer’s disease cases

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Malarte, Mona-Lisa, Nordberg, Agneta, Lemoine, Laetitia·2021·European Journal of Nuclear Medicine and Molecular Imaging

Abstract

Abstract Purpose MK6240 is a second-generation tau PET tracer designed to detect the neurofibrillary tangles in the brains of patients with Alzheimer’s disease (AD). The aim of the study was to characterize 3H-MK6240 in AD and control brain tissue and to compare its binding properties with those of first-generation tau PET tracers. Methods Saturation binding assays with 3H-MK6240 were carried out in the temporal and parietal cortices of AD brains to determine the maximum number of binding sites (Bmax) and the dissociation constants (Kd) at these sites. Competitive binding assays were carried out between 3H-MK6240 and unlabelled MK6240, AV-1451 (aka T807, flortaucipir) and THK5117, and between 3H-THK5351 and unlabelled MK6240. Regional binding studies with 3H-MK6240 were carried out in homogenates from six AD and seven control brains and, using autoradiography, on large frozen sections from two AD brains and one control brain. Results The saturation binding assays gave Bmax and Kd values of 59.2 fmol/mg and 0.32 nM in the temporal cortex and 154.7 fmol/mg and 0.15 nM in the parietal cortex. The competitive binding assays revealed two binding sites with affinities in the picomolar and nanomolar range shared by 3H-MK6240 and all the tested unlabelled compounds. There were no binding sites in common between 3H-THK5351 and unlabelled MK6240. Regional binding of 3H-MK6240 was significantly higher in AD brain tissue than in controls. Binding in brain tissue from AD patients with early-onset AD was significantly higher than in brain tissue from patients with late-onset AD. Binding of 3H-MK6240 was not observed in off-target regions. Autoradiography showed high regional cortical binding in the two AD brains and very low binding in the control brain. Conclusions 3H-MK6240 has a high binding affinity for tau deposits in AD brain tissue but also has different binding characteristics from those of the first-generation tau tracers. This confirms the complexity of tau tracer binding on tau deposits with different binding affinities for different binding sites.

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  • [18F]MK6240 detects paired helical filament (PHF) tau and has shown a high binding affinity for brain homogenate rich in NFTs.

    “[18F]MK6240 detects paired helical filament (PHF) tau and has shown a high binding affinity for brain homogenate rich in NFTs.61”

    From Cerebrospinal fluid p-tau231 as an early indicator of emerging pathology in Alzheimer's disease (2022) · cites this paper as [61]

    The Introduction reports high affinity of MK6240 for NFT-rich brain homogenate, and the paper’s binding assays support high affinity for tau deposits in Alzheimer’s disease tissue. The copy describes binding to tau fibrils but does not specifically identify the detected tau as paired helical filament (PHF) tau. Its own tissue-binding experiments used 3H-MK6240 rather than 18F-MK6240. (LLM, conf=0.84)

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Authors
Malarte, M.-L., Nordberg, A., & Lemoine, L.
Affiliations
  • Karolinska Institutet (SE)
  • Karolinska University Hospital (SE)
Venue
European Journal of Nuclear Medicine and Molecular Imaging
Published
2020-09-24
Volume
48
Issue
4
Pages
1093-1102
ISSN
  • 1619-7070 (ISSN-L)
  • 1619-7089
OpenAlex
W3087816312
Cited by
41
References
5
Citations by year
2026: 2 · 2025: 10 · 2024: 8 · 2023: 10 · 2022: 8 · 2021: 3
FWCI
3.16
Type
journal article
Language
en
Open access
Locations
  • European Journal of Nuclear Medicine and Molecular Imaging (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
Funders
  • Stiftelsen för Strategisk Forskning (RB13-0192)
  • Vetenskapsrådet
  • Hjärnfonden
  • Stockholms Läns Landsting
  • Alzheimerfonden
  • Stiftelsen för Gamla Tjänarinnor
  • Gun och Bertil Stohnes Stiftelse
  • Gunvor och Josef Anérs stiftelsen
  • Loo och Hans Ostermans Stiftelse
  • Tore Nilsons Stiftelse för Medicinsk Forskning
  • KI Foundation for Geriatric Diseases
  • Demensfonden
Topics
  • Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
  • Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
  • Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Medical Imaging Techniques and Applications
Keywords
tau PET tracers, Alzheimer's disease, neurofibrillary tangles, binding affinity, dissociation constant, binding sites, flortaucipir, early-onset Alzheimer's disease, late-onset Alzheimer's disease, off-target binding, autoradiography, temporal cortex
MeSH terms
Alzheimer Disease, Autopsy, Brain, Humans, Neurofibrillary Tangles, tau Proteins, Positron-Emission Tomography

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