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1.
Proteins ; 82(10): 2318-31, 2014 Oct.
Article in English | MEDLINE | ID: mdl-24752983

ABSTRACT

Proteins are biosynthesized from N to C terminus before they depart from the ribosome and reach their bioactive state in the cell. At present, very little is known about the evolution of conformation and the free energy of the nascent protein with chain elongation. These parameters critically affect the extent of folding during ribosome-assisted biosynthesis. Here, we address the impact of vectorial amino acid addition on the burial of nonpolar surface area and on the free energy of native-like structure formation in the absence of the ribosomal machinery. We focus on computational predictions on proteins bearing the globin fold, which is known to encompass the 3/3, 2/2, and archaeal subclasses. We find that the burial of nonpolar surface increases progressively with chain elongation, leading to native-like conformations upon addition of the last C-terminal residues, corresponding to incorporation of the last two helices. Additionally, the predicted folding entropy for generating native-like structures becomes less unfavorable at nearly complete chain lengths, suggesting a link between the late burial of nonpolar surface and water release. Finally, the predicted folding free energy takes a progressive favorable dip toward more negative values, as the chain gets longer. These results suggest that thermodynamic stabilization of the native structure of newly synthesized globins during translation in the cell is significantly enhanced as the chain elongates. This is especially true upon departure of the last C-terminal residues from the ribosomal tunnel, which hosts ca., 30-40 amino acids. Hence, we propose that release from the ribosome is a crucial step in the life of single-domain proteins in the cell.


Subject(s)
Archaea/chemistry , Globins/chemistry , Peptide Chain Elongation, Translational , Protein Folding , Ribosomes/chemistry , Thermodynamics , Entropy , Hydrophobic and Hydrophilic Interactions , Models, Molecular , Protein Conformation , Protein Structure, Tertiary
2.
N S W Public Health Bull ; 18(3-4): 48-50, 2007.
Article in English | MEDLINE | ID: mdl-17601404

ABSTRACT

Human health in our cities is an expression of complex social and environmental interactions not previously faced in our long evolutionary history. In this paper, we present a social-ecological perspective on the complex nature of emerging public health problems in cities and identify some of the research questions emerging from this new view of the city. We argue that an integrative urban science agenda is needed not only to inform urban policy, planning and design, but also to alert people to the consequences of and trade-offs around their choices and behaviours.


Subject(s)
Environmental Health/trends , Public Health/trends , Urban Health/trends , Ecosystem , Humans , Social Environment
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