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  • 1
    Publication Date: 2010-11-13
    Description: 〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Reid, W V -- Chen, D -- Goldfarb, L -- Hackmann, H -- Lee, Y T -- Mokhele, K -- Ostrom, E -- Raivio, K -- Rockstrom, J -- Schellnhuber, H J -- Whyte, A -- New York, N.Y. -- Science. 2010 Nov 12;330(6006):916-7. doi: 10.1126/science.1196263.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉David and Lucile Packard Foundation, Los Altos, CA 94022, USA. wreid@packard.org〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/21071651" target="_blank"〉PubMed〈/a〉
    Keywords: *Conservation of Natural Resources ; *Environment ; Humans ; *International Cooperation ; *Policy ; *Research
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 2
    Publication Date: 2010-10-16
    Description: 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.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Rimer, Jeffrey D -- An, Zhihua -- Zhu, Zina -- Lee, Michael H -- Goldfarb, David S -- Wesson, Jeffrey A -- Ward, Michael D -- 1U54DK083908-01/DK/NIDDK NIH HHS/ -- R01 DK068551/DK/NIDDK NIH HHS/ -- R01-DK068551/DK/NIDDK NIH HHS/ -- New York, N.Y. -- Science. 2010 Oct 15;330(6002):337-41. doi: 10.1126/science.1191968.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Chemistry and the Molecular Design Institute, New York University (NYU), 100 Washington Square East, New York, NY 10003-6688, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/20947757" target="_blank"〉PubMed〈/a〉
    Keywords: Binding Sites ; Crystallization ; Cystine/*analogs & derivatives/*chemistry/metabolism/pharmacology ; Cystinuria/complications/*drug therapy ; Drug Design ; Humans ; Hydrogen Bonding ; Kidney Calculi/chemistry/etiology/*prevention & control ; Microscopy, Atomic Force ; Models, Molecular ; Molecular Mimicry ; Molecular Structure ; Physicochemical Processes ; Solubility
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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