Literature DB >> 20057046

Overcoming merohedral twinning in crystals of bacteriorhodopsin grown in lipidic mesophase.

Valentin Borshchevskiy1, Rouslan Efremov, Ekaterina Moiseeva, Georg Büldt, Valentin Gordeliy.   

Abstract

Twinning is one of the most common crystal-growth defects in protein crystallography. There are neither efficient rational approaches for the growth of nontwinned protein crystals nor are there examples of systematic studies of the dependence of the twinning-ratio distribution on crystallization conditions. The description of the twinning phenomenon has been covered even less for membrane-protein crystals and is non-existent for crystals grown using lipidic phases (in meso). In the present work, possibilities for overcoming merohedral twinning are investigated for crystals of the membrane protein bacteriorhodopsin (bR) grown in meso. It is shown that traditional crystallization additives are not effective in the case of the in meso crystallization of bR. The twinning ratio was determined for 310 crystals grown under different crystallization conditions. A correlation of the twinning ratio with the growth rate of the crystals was observed. Slow growth indicated that crystals had a noticeable chance of avoiding twinning. Model calculations were performed in order to rationalize this observation. The calculations confirmed the experimental observation that most crystals consist of two twin domains and showed that under this condition small changes in the probability of twin-domain formation lead to dramatic changes in the number of nontwinned crystals, which explains why slow crystal growth results in a considerable number of nontwinned crystals.

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Year:  2009        PMID: 20057046     DOI: 10.1107/S0907444909042838

Source DB:  PubMed          Journal:  Acta Crystallogr D Biol Crystallogr        ISSN: 0907-4449


  5 in total

1.  Polarization-resolved second-harmonic generation microscopy as a method to visualize protein-crystal domains.

Authors:  Emma L DeWalt; Victoria J Begue; Judith A Ronau; Shane Z Sullivan; Chittaranjan Das; Garth J Simpson
Journal:  Acta Crystallogr D Biol Crystallogr       Date:  2012-12-20

2.  Reduction of lattice disorder in protein crystals by high-pressure cryocooling.

Authors:  Qingqiu Huang; Sol M Gruner; Chae Un Kim; Yuxin Mao; Xiaochun Wu; Doletha M E Szebenyi
Journal:  J Appl Crystallogr       Date:  2016-02-01       Impact factor: 3.304

3.  Microbial Rhodopsins.

Authors:  Valentin Gordeliy; Kirill Kovalev; Ernst Bamberg; Francisco Rodriguez-Valera; Egor Zinovev; Dmitrii Zabelskii; Alexey Alekseev; Riccardo Rosselli; Ivan Gushchin; Ivan Okhrimenko
Journal:  Methods Mol Biol       Date:  2022

4.  Crystal structure of Escherichia coli-expressed Haloarcula marismortui bacteriorhodopsin I in the trimeric form.

Authors:  Vitaly Shevchenko; Ivan Gushchin; Vitaly Polovinkin; Ekaterina Round; Valentin Borshchevskiy; Petr Utrobin; Alexander Popov; Taras Balandin; Georg Büldt; Valentin Gordeliy
Journal:  PLoS One       Date:  2014-12-05       Impact factor: 3.240

5.  Recovery of data from perfectly twinned virus crystals revisited.

Authors:  Helen Mary Ginn; David Ian Stuart
Journal:  Acta Crystallogr D Struct Biol       Date:  2016-05-25       Impact factor: 7.652

  5 in total

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