The positions of water molecules have been analyzed in high quality protein X-ray crystal structures.About 70% of these water molecules are in contact with protein atoms at the protein surface and constitutethe first hydration layer. About 20% of them are close to the first hydration layer but are not in contactwith protein atoms and constitute the second hydration layer. The rest of the water molecules are eitherburied in the protein core or close to hetero-atoms (inorganic ions and small organic molecules). Upperlayers (third, fourth, etc.) are not observed in the dataset of protein crystal structures examined here.Water molecules of both layers are not, in general, surrounded by a tetrahedral arrangement of atoms,as it should be expected on the basis of the electronic structure of water. Usually there are less thanfour atoms around water molecules and even when there are four atoms, the stereochemistry is oftendistorted. Water molecules are more mobile than protein atoms, more in the second hydration layer thanin the first.

Protein hydration: Investigation of globular protein crystal structures

CARUGO, OLIVIERO ITALO
2017-01-01

Abstract

The positions of water molecules have been analyzed in high quality protein X-ray crystal structures.About 70% of these water molecules are in contact with protein atoms at the protein surface and constitutethe first hydration layer. About 20% of them are close to the first hydration layer but are not in contactwith protein atoms and constitute the second hydration layer. The rest of the water molecules are eitherburied in the protein core or close to hetero-atoms (inorganic ions and small organic molecules). Upperlayers (third, fourth, etc.) are not observed in the dataset of protein crystal structures examined here.Water molecules of both layers are not, in general, surrounded by a tetrahedral arrangement of atoms,as it should be expected on the basis of the electronic structure of water. Usually there are less thanfour atoms around water molecules and even when there are four atoms, the stereochemistry is oftendistorted. Water molecules are more mobile than protein atoms, more in the second hydration layer thanin the first.
2017
Biochemistry & Biophysics focuses on the structure and chemistry of biomolecules and covers all aspects of basic biochemistry/biophysics, including molecular structure, enzyme kinetics and protein-protein interaction; this category also contains cross-disciplinary resources focused on a specific class of biological molecules, e.g., nucleic acids, steroids, magnesium, growth factors, free radicals, bio-membranes, and peptides. Excluded are resources dealing with the application of biochemical techniques to specific topics listed elsewhere in CC/LS. Resources with a strong emphasis on the integration of biochemical pathways (such as signal transduction or molecular motors) at the cellular level are placed in the Cell & Developmental Biology category.
Chemistry & Analysis covers research on natural and laboratory syntheses, chemical structure, structure-function relationship, isolation and analyses of biologically significant molecules, medicinal and food chemistry. Technical material describing crucial chemical methods in biochemical analysis and research is also placed in this category. Resources covering general biochemistry and natural metabolic pathways are excluded.
Esperti anonimi
Inglese
Internazionale
STAMPA
99
160
165
6
Protein structure, Protein hydration, Protein Data Bank, Structural biology, Water chemistry
http://www.sciencedirect.com/science/article/pii/S0141813017301332
no
1
info:eu-repo/semantics/article
262
Carugo, OLIVIERO ITALO
1 Contributo su Rivista::1.1 Articolo in rivista
none
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/1180246
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