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1H detection and dynamic nuclear polarization–enhanced NMR of Aβ1-42 fibrils

Bahri, Salima (author)
Massachusetts Institute of Technology
Silvers, Robert (author)
Florida State University
Michael, Brian (author)
Massachusetts Institute of Technology
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Jaudzems, Kristaps (author)
Ecole Normale Superieure de Lyon
Lalli, Daniela (author)
Ecole Normale Superieure de Lyon
Casano, Gilles (author)
Aix-Marseille University
Ouari, Olivier (author)
Aix-Marseille University
Lesage, Anne (author)
Ecole Normale Superieure de Lyon
Pintacuda, Guido (author)
Ecole Normale Superieure de Lyon
Linse, Sara (author)
Lund University,Lunds universitet,NanoLund: Centre for Nanoscience,Annan verksamhet, LTH,Lunds Tekniska Högskola,Biokemi och Strukturbiologi,Centrum för Molekylär Proteinvetenskap,Kemiska institutionen,Institutioner vid LTH,Other operations, LTH,Faculty of Engineering, LTH,Biochemistry and Structural Biology,Center for Molecular Protein Science,Department of Chemistry,Departments at LTH,Faculty of Engineering, LTH
Griffin, Robert G. (author)
Massachusetts Institute of Technology
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 (creator_code:org_t)
2021-12-30
2022
English.
In: Proceedings of the National Academy of Sciences of the United States of America. - : Proceedings of the National Academy of Sciences. - 0027-8424. ; 119:1
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Several publications describing high-resolution structures of amyloid-β (Aβ) and other fibrils have demonstrated that magic-angle spinning (MAS) NMR spectroscopy is an ideal tool for studying amyloids at atomic resolution. Nonetheless, MAS NMR suffers from low sensitivity, requiring relatively large amounts of samples and extensive signal acquisition periods, which in turn limits the questions that can be addressed by atomic-level spectroscopic studies. Here, we show that these drawbacks are removed by utilizing two relatively recent additions to the repertoire of MAS NMR experiments—namely, 1H detection and dynamic nuclear polarization (DNP). We show resolved and sensitive two-dimensional (2D) and three-dimensional (3D) correlations obtained on 13C,15N-enriched, and fully protonated samples of M0Aβ1-42 fibrils by high-field 1H-detected NMR at 23.4 T and 18.8 T, and 13C-detected DNP MAS NMR at 18.8 T. These spectra enable nearly complete resonance assignment of the core of M0Aβ1-42 (K16-A42) using submilligram sample quantities, as well as the detection of numerous unambiguous internuclear proximities defining both the structure of the core and the arrangement of the different monomers. An estimate of the sensitivity of the two approaches indicates that the DNP experiments are currently ∼6.5 times more sensitive than 1H detection. These results suggest that 1H detection and DNP may be the spectroscopic approaches of choice for future studies of Aβ and other amyloid systems.

Subject headings

NATURVETENSKAP  -- Kemi -- Fysikalisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Physical Chemistry (hsv//eng)

Keyword

H detection
Amyloid β
Dynamic nuclear polarization
Magic-angle spinning

Publication and Content Type

art (subject category)
ref (subject category)

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