| Literature DB >> 19903529 |
G Zhao1, M C Johnson, J R Schnell, Y Kanaoka, W Haase, D Irikura, B K Lam, I Schmidt-Krey.
Abstract
Human leukotriene C(4) synthase (LTC(4)S) forms highly ordered two-dimensional (2D) crystals under specific reconstitution conditions. It was found that control of a larger number of parameters than is usually observed for 2D crystallization of membrane proteins was necessary to induce crystal formation of LTC(4)S. Here, we describe the parameters that were optimized to yield large and well-ordered 2D crystals of LTC(4)S. Careful fractioning of eluates during the protein purification was essential for obtaining crystals. While the lipid-to-protein ratio was critical in obtaining order, four parameters were decisive in inducing growth of crystals that were up to several microns in size. To obtain a favorable diameter, salt, temperature, glycerol, and initial detergent concentration had to be controlled with great care. Interestingly, several crystal forms could be grown, namely the plane group symmetries of p2, p3, p312, and two different unit cell sizes of plane group symmetry p321. (c) 2009 Elsevier Inc. All rights reserved.Entities:
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Year: 2009 PMID: 19903529 PMCID: PMC2826519 DOI: 10.1016/j.jsb.2009.11.002
Source DB: PubMed Journal: J Struct Biol ISSN: 1047-8477 Impact factor: 2.867