期刊
CHEMICAL COMMUNICATIONS
卷 51, 期 81, 页码 15055-15058出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c5cc04618a
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资金
- US National Science Foundation [CHE 957793, CHE 1310363]
- NIH HEI grant [1S10 RR025105]
- NIH RO1 grant [9R01GM098033]
- Grants-in-Aid for Scientific Research [26248050, 26119005] Funding Source: KAKEN
- NATIONAL CENTER FOR RESEARCH RESOURCES [S10RR025105] Funding Source: NIH RePORTER
- NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM098033] Funding Source: NIH RePORTER
We present a 3D H-1-detected solid-state NMR (SSNMR) approach for main-chain signal assignments of 10-100 nmol of fully protonated proteins using ultra-fast magic-angle spinning (MAS) at similar to 80 kHz by a novel spectral-editing method, which permits drastic spectral simplification. The approach offers similar to 110 fold time saving over a traditional 3D C-13-detected SSNMR approach.
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