(Fig.1) Medical research cannot clarify atomic mechanism nor cure diseases due to bad electron microscopes that cannot see atoms.
The present medical research (and hyped AI ) has been deadend with No progress (= still No cures for cancers or Alzheimer ).
Because the best mainstream method for clarifying molecular mechanisms in medical research has been (useless) hyped cryo-electron microscope (= cryo-EM ), which can Not clarify atomic mechanism due to its bad resolution ( this-limitations of cryo EM ), since 1970 (= No progress for long years, this-history ).
Only multi-probe atomic force microscopes (= newer than the old electron microscopy ) can directly see and clarify atomic mechanism of proteins for curing diseases, which has been hampered by the unreal quantum mechanical atomic model for a long time.
The 2nd, 3rd paragraphs of this hyped news (8/21/2025) say
"a team of researchers.. has succeeded in establishing the first comprehensive transport model of the plasma membrane Ca2+-ATPase (PMCA) by resolving its 3D structure" ← fake news
"This mechanism could be a promising (= still useless ) starting point for developing new drugs"
↑ This research paper ↓
p.2-left-2nd-paragraph says "we determined an ensemble of PMCA2 (= plasma membrane Ca2+-ATPase ) structures.. by cryo-electron microscopy (cryo-EM)"
p.2-right-2nd-paragraph says
"The eight resulting structures of PMCA2 had an overall resolution
ranging from 2.8 Å to 3.6 Å. ← Cryo-electron microscopes are useless, unable to get atomic resolution of less than 1Å (= each atomic size is less than 1 angstrom or 1Å, this-middle-picture's cryo-EM's resolution is worse than the atomic 1Å = 1 Angstrom resolution )
p.13-right-1st-paragraph says "Because the local resolution of Ig1 was still too low to allow for de novo modelling"
p.25-even this latest Cryo-EM's (map) resolution was too bad (= 6.3Å, 9.5Å, this-p.3-p.6-local resolution ), which cannot clarify atomic mechanism (of proteins or diseases ) needing less than 1Å resolution, so cannot cure cancers or Alzheimer.
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