Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/130794
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Type: Journal article
Title: Simplified heavy-atom derivatization of protein structures via co-crystallization with the MAD tetragon tetrabromoterephthalic acid
Author: Truong, J.Q.
Nguyen, S.
Bruning, J.B.
Shearwin, K.E.
Citation: Acta Crystallographica Section F: Structural Biology Communications, 2021; 77(5):156-162
Publisher: International Union of Crystallography
Issue Date: 2021
ISSN: 2053-230X
2053-230X
Statement of
Responsibility: 
J. Q. Truong, S. Nguyen, J. B. Bruning and K. E. Shearwin
Abstract: The phase problem is a persistent bottleneck that impedes the structure-determination pipeline and must be solved to obtain atomic resolution crystal structures of macromolecules. Although molecular replacement has become the predominant method of solving the phase problem, many scenarios still exist in which experimental phasing is needed. Here, a proof-of-concept study is presented that shows the efficacy of using tetrabromoterephthalic acid (B4C) as an experimental phasing compound. Incorporating B4C into the crystal lattice using co-crystallization, the crystal structure of hen egg-white lysozyme was solved using MAD phasing. The strong anomalous signal generated by its four Br atoms coupled with its compatibility with commonly used crystallization reagents render B4C an effective experimental phasing compound that can be used to overcome the phase problem.
Keywords: Crystallography; experimental phasing; B4C; tetrabromoterephthalic acid; lysozyme; co-crystallization
Rights: Copyright status unknown
DOI: 10.1107/s2053230x21004052
Grant ID: http://purl.org/au-research/grants/arc/DP160101450
http://purl.org/au-research/grants/arc/DP150103009
Published version: http://dx.doi.org/10.1107/s2053230x21004052
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Biochemistry publications

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