We describe a general and simple modification to the standard M9 minimal medium recipe that leads to an approximate twofold increase in the yield of heterologously expressed proteins in Escherichia coli BL21(DE3) bacteria. We monitored the growth of bacteria transformed with plasmids for three different test proteins in five minimal media with different concentrations of buffering salts and/or initial media pH. After purification of the over-expressed proteins, we found a clear correlation between the protein yield and change in media pH over time, where the minimal media that were the most buffered and therefore most resistant to change in pH produced the most protein. And in all three test protein cases, the difference in yield was nearly twofold between the best and worst buffering media. Thus, we propose that increasing the buffering capacity of M9 minimal media will generally lead to a similar increase for most of the proteins currently produced by this standard protein expression protocol. Moreover, we have qualitatively found that this effect also extends to deuterated M9 minimal media growths, which could lead to significant cost savings in these preparations.
Minimal NMR distance information for rigidity of protein graphs
Minimal NMR distance information for rigidity of protein graphs
Publication date: Available online 26 April 2018
Source:Discrete Applied Mathematics</br>
Author(s): Carlile Lavor, Leo Liberti, Bruce Donald, Bradley Worley, Benjamin Bardiaux, Thérèse E. Malliavin, Michael Nilges</br>
Nuclear Magnetic Resonance (NMR) experiments provide distances between nearby atoms of a protein molecule. The corresponding structure determination problem is to determine the 3D protein structure by exploiting such distances. We present a new order on the atoms of the...
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04-27-2018 05:00 AM
Increasing the amount of information that can be extracted from a protein microarray - Phys.Org
Increasing the amount of information that can be extracted from a protein microarray - Phys.Org
http://www.bionmr.com//t1.gstatic.com/images?q=tbn:ANd9GcSfIXTe4vaQTrvYQNnsa8m-YENwfi7xUyWRmkkYYO0YpRLWCvKdecVtJWLFfZGwKnReajxqdNU
Phys.Org
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Increasing the amount of information that can be extracted from a protein microarray
Phys.Org
The approach will nicely complement and supplement existing techniques, used for protein characterization, such as CD, NMR and mass spectrometry," commented Biomedical Spectroscopy and Imaging Editor-in-Chief Dr. Parvez I....
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06-03-2016 04:52 PM
Protein Crystallization Market: Driven By: Increasing technological ... - Medgadget.com (blog)
Protein Crystallization Market: Driven By: Increasing technological ... - Medgadget.com (blog)
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Protein Crystallization Market: Driven By: Increasing technological ...
Medgadget.com (blog)
Various techniques used during protein crystallization technology are ion-exchange chromatography, high-performance liquid chromatography (HPLC), gel-electrophoresis, x-ray crystallography and nuclear magnetic resonance (NMR). On the basis of ...
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12-17-2015 01:53 PM
Protein Crystallization Market: Increasing spending in research and ... - Medgadget.com (blog)
Protein Crystallization Market: Increasing spending in research and ... - Medgadget.com (blog)
<img alt="" height="1" width="1">
Protein Crystallization Market: Increasing spending in research and ...
Medgadget.com (blog)
Various techniques used during protein crystallization technology are ion-exchange chromatography, high-performance liquid chromatography (HPLC), gel-electrophoresis, x-ray crystallography and nuclear magnetic resonance (NMR). On the basis of ...
and more »
Read here
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12-15-2015 08:09 PM
Phenotypic Screening Identifies Protein Synthesis Inhibitors as H-Ras-Nanocluster-Increasing Tumor Growth Inducers
Phenotypic Screening Identifies Protein Synthesis Inhibitors as H-Ras-Nanocluster-Increasing Tumor Growth Inducers
http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/bichaw/0/bichaw.ahead-of-print/acs.biochem.5b00724/20151130/images/medium/bi-2015-00724w_0004.gif
Biochemistry
DOI: 10.1021/acs.biochem.5b00724
http://feeds.feedburner.com/~ff/acs/bichaw?d=yIl2AUoC8zA
http://feeds.feedburner.com/~r/acs/bichaw/~4/J39aNiUlZbQ
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11-30-2015 09:39 PM
TD NMR as a method to determine and characterize the water-binding capacity of whey protein microparticles
TD NMR as a method to determine and characterize the water-binding capacity of whey protein microparticles
Publication date: Available online 9 October 2015
Source:Food Hydrocolloids</br>
Author(s): Jorien P.C.M. Peters, Frank J. Vergeldt, Henk Van As, Hannemieke Luyten, Remko M. Boom, Atze Jan van der Goot</br>
Water-binding capacity (WBC) is commonly measured with a centrifugation method in which a sample is hydrated in excess water and the pellet weight after centrifugation defines the WBC. When a dispersion is being analyzed, here containing whey...
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10-10-2015 06:11 AM
Increasing Throughput in Protein Thermal Shift Assays - Genetic Engineering & Biotechnology News
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Increasing Throughput in Protein Thermal Shift Assays
Genetic Engineering & Biotechnology News
Historically, protein interaction studies have been measured using an array of techniques, including nuclear magnetic resonance, differential scanning calorimetry, and surface plasma resonance imaging. Additionally, protein melt screening methods used ...
Increasing Throughput in Protein Thermal Shift Assays - Genetic Engineering & Biotechnology News
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04-11-2015 12:04 AM
[NMR paper] Contributions to protein entropy and heat capacity from bond vector motions measured
Contributions to protein entropy and heat capacity from bond vector motions measured by NMR spin relaxation.
http://www.ncbi.nlm.nih.gov/corehtml/query/egifs/http:--linkinghub.elsevier.com-ihub-images-PubMedLink.gif Related Articles Contributions to protein entropy and heat capacity from bond vector motions measured by NMR spin relaxation.
J Mol Biol. 1997 Oct 10;272(5):790-804
Authors: Yang D, Mok YK, Forman-Kay JD, Farrow NA, Kay LE
The backbone dynamics of both folded and unfolded states of staphylococcal nuclease (SNase) and the N-terminal...