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  • 1
    Publication Date: 2012-11-23
    Description: Hydrophobic hydration is considered to have a key role in biological processes ranging from membrane formation to protein folding and ligand binding. Historically, hydrophobic hydration shells were thought to resemble solid clathrate hydrates, with solutes surrounded by polyhedral cages composed of tetrahedrally hydrogen-bonded water molecules. But more recent experimental and theoretical studies have challenged this view and emphasized the importance of the length scales involved. Here we report combined polarized, isotopic and temperature-dependent Raman scattering measurements with multivariate curve resolution (Raman-MCR) that explore hydrophobic hydration by mapping the vibrational spectroscopic features arising from the hydrophobic hydration shells of linear alcohols ranging from methanol to heptanol. Our data, covering the entire 0-100 degrees C temperature range, show clear evidence that at low temperatures the hydration shells have a hydrophobically enhanced water structure with greater tetrahedral order and fewer weak hydrogen bonds than the surrounding bulk water. This structure disappears with increasing temperature and is then, for hydrophobic chains longer than ~1 nm, replaced by a more disordered structure with weaker hydrogen bonds than bulk water. These observations support our current understanding of hydrophobic hydration, including the thermally induced water structural transformation that is suggestive of the hydrophobic crossover predicted to occur at lengths of ~1 nm (refs 5, 9, 10, 14).〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Davis, Joel G -- Gierszal, Kamil P -- Wang, Ping -- Ben-Amotz, Dor -- England -- Nature. 2012 Nov 22;491(7425):582-5. doi: 10.1038/nature11570.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Purdue University, Department of Chemistry, West Lafayette, Indiana 47907, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23172216" target="_blank"〉PubMed〈/a〉
    Keywords: 1-Butanol/chemistry ; Hydrogen Bonding ; *Hydrophobic and Hydrophilic Interactions ; Molecular Structure ; Spectrum Analysis, Raman ; Temperature ; Vibration ; Water/*chemistry
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 2
    Publication Date: 1995-02-17
    Description: Molecular biological studies of the mammalian inner ear have been limited by the relatively small size of the sensory endorgans contained within. The saccular otolithic organ in teleostian fish is structurally similar to its mammalian counterpart but can contain an order of magnitude more sensory cells. The prospect of the evolutionary conservation of proteins utilized in the vertebrate inner ear and the relative abundance of teleostian saccular sensory tissue made this an attractive system for molecular biological studies. A complementary DNA obtained by differential screening of a saccular complementary DNA library was identified that encodes an inner ear-specific collagen molecule.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Davis, J G -- Oberholtzer, J C -- Burns, F R -- Greene, M I -- 5 T32 NS07064-13/NS/NINDS NIH HHS/ -- K08-DC00069/DC/NIDCD NIH HHS/ -- New York, N.Y. -- Science. 1995 Feb 17;267(5200):1031-4.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Pathology and Laboratory Medicine, University of Pennsylvania School of Medicine, Philadelphia 19104.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/7863331" target="_blank"〉PubMed〈/a〉
    Keywords: Amino Acid Sequence ; Animals ; *Cloning, Molecular ; Collagen/*chemistry/*genetics ; DNA, Complementary/genetics ; *Extracellular Matrix Proteins ; *Fish Proteins ; Fishes/*genetics ; Gene Expression ; In Situ Hybridization ; Molecular Sequence Data ; Otolithic Membrane/chemistry ; RNA, Messenger/analysis/genetics ; Saccule and Utricle/*chemistry
    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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