| Literature DB >> 20947757 |
Jeffrey D Rimer1, Zhihua An1, Zina Zhu1, Michael H Lee1, David S Goldfarb2, Jeffrey A Wesson3, Michael D Ward1.
Abstract
Crystallization of L-cystine is a critical step in the pathogenesis of cystine kidney stones. Treatments for this disease are somewhat effective but often lead to adverse side effects. Real-time in situ atomic force microscopy (AFM) reveals that L-cystine dimethylester (L-CDME) and L-cystine methylester (L-CME) dramatically reduce the growth velocity of the six symmetry-equivalent {100} steps because of specific binding at the crystal surface, which frustrates the attachment of L-cystine molecules. L-CDME and L-CME produce l-cystine crystals with different habits that reveal distinct binding modes at the crystal surfaces. The AFM observations are mirrored by reduced crystal yield and crystal size in the presence of L-CDME and L-CME, collectively suggesting a new pathway to the prevention of L-cystine stones by rational design of crystal growth inhibitors.Entities:
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Year: 2010 PMID: 20947757 PMCID: PMC5166609 DOI: 10.1126/science.1191968
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728