[ASAP] Controlled and Stable Patterning of Diverse Inorganic Nanocrystals on Crystalline Two-Dimensional Protein Arrays
Controlled and Stable Patterning of Diverse Inorganic Nanocrystals on Crystalline Two-Dimensional Protein Arrays
https://pubs.acs.org/na101/home/literatum/publisher/achs/journals/content/bichaw/0/bichaw.ahead-of-print/acs.biochem.1c00032/20210310/images/medium/bi1c00032_0007.gif
Biochemistry
DOI: 10.1021/acs.biochem.1c00032
http://feeds.feedburner.com/~r/acs/bichaw/~4/D7g5AaXCZWc
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nmrlearner
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03-11-2021 06:03 AM
[ASAP] 19F Dynamic Nuclear Polarization at Fast Magic Angle Spinning for NMR of HIV-1 Capsid Protein Assemblies
19F Dynamic Nuclear Polarization at Fast Magic Angle Spinning for NMR of HIV-1 Capsid Protein Assemblies
Manman Lu, Mingzhang Wang, Ivan V. Sergeyev, Caitlin M. Quinn, Jochem Struppe, Melanie Rosay, Werner Maas, Angela M. Gronenborn, Tatyana Polenova
https://pubs.acs.org/appl/literatum/publisher/achs/journals/content/jacsat/0/jacsat.ahead-of-print/jacs.8b09216/20190329/images/medium/ja-2018-09216b_0006.gif
Journal of the American Chemical Society
DOI: 10.1021/jacs.8b09216
http://feeds.feedburner.com/~ff/acs/jacsat?d=yIl2AUoC8zA...
nmrlearner
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04-02-2019 01:35 AM
[NMR paper] Dicarboxylate-Oside Detergents for Extraction, Overstabilization and Crystallization of Membrane Proteins
Dicarboxylate-Oside Detergents for Extraction, Overstabilization and Crystallization of Membrane Proteins
To tackle the problem of membrane proteins (MPs) instability in detergent solutions, we designed a series of dicarboxylate-oside detergents (DCODs) in which we optimized the polar head to clamp the membrane domain, including on one side a cluster of two carboxyl groups that promotes salt-bridges with basic residues abundant at the membrane-cytoplasm interface of MPs, and on the other side a sugar to generate H-bonds. Tested on BmrA, an ATP-binding cassette pump, DCODs 8b, 8c, and 9b...
Cell-free expression and stable isotope labelling strategies for membrane proteins
Cell-free expression and stable isotope labelling strategies for membrane proteins
Abstract Membrane proteins are highly underrepresented in the structural data-base and remain one of the most challenging targets for functional and structural elucidation. Their roles in transport and cellular communication, furthermore, often make over-expression toxic to their host, and their hydrophobicity and structural complexity make isolation and reconstitution a complicated task, especially in cases where proteins are targeted to inclusion bodies. The development of cell-free expression systems...
nmrlearner
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01-09-2011 12:46 PM
[NMR paper] An evaluation of detergents for NMR structural studies of membrane proteins.
An evaluation of detergents for NMR structural studies of membrane proteins.
Related Articles An evaluation of detergents for NMR structural studies of membrane proteins.
J Biomol NMR. 2004 Jan;28(1):43-57
Authors: Krueger-Koplin RD, Sorgen PL, Krueger-Koplin ST, Rivera-Torres IO, Cahill SM, Hicks DB, Grinius L, Krulwich TA, Girvin ME
Structural information on membrane proteins lags far behind that on soluble proteins, in large part due to difficulties producing homogeneous, stable, structurally relevant samples in a membrane-like environment....
nmrlearner
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11-24-2010 09:25 PM
[NMR paper] Porcine cerebroside sulfate activator (saposin B) secondary structure: CD, FTIR, and
Porcine cerebroside sulfate activator (saposin B) secondary structure: CD, FTIR, and NMR studies.
Related Articles Porcine cerebroside sulfate activator (saposin B) secondary structure: CD, FTIR, and NMR studies.
Mol Genet Metab. 1998 Jan;63(1):14-25
Authors: Waring AJ, Chen Y, Faull KF, Stevens R, Sherman MA, Fluharty AL
Cerebroside sulfate activator protein (CSAct or saposin B) is one of a group of heat stable, low-molecular-weight proteins that appear to share a common structural motif. These have been referred to as saposin-like proteins...
nmrlearner
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11-17-2010 11:06 PM
An economical method for producing stable-isotope labeled proteins by the E. coli cel
An economical method for producing stable-isotope labeled proteins by the E. coli cell-free system
Abstract Improvement of the cell-free protein synthesis system (CF) over the past decade have made it one of the most powerful protein production methods. The CF approach is especially useful for stable-isotope (SI) labeling of proteins for NMR analysis. However, it is less popular than expected, partly because the SI-labeled amino acids used for SI labeling by the CF are too expensive. In the present study, we developed a simple and inexpensive method for producing an SI-labeled protein...