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1ale

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==Overview==
==Overview==
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Peptides corresponding to the proposed lipid-binding domains of human, apolipoprotein C-I, residues 7-24 (ALDKLKEFGNTLEDKARE) and 35-53, (SAKMREWFSETFQKVKEKL), were studied by CD and two-dimensional 1H NMR, spectroscopy. Sodium dodecyl sulfate (SDS) was used to model the, lipoprotein environment. Analysis of the CD data shows that both peptides, lack well-defined structure in aqueous solution but adopt helical, ordered, structures upon the addition of SDS. The helical nature of the peptides in, the presence of SDS was confirmed by H alpha secondary shifts. A total of, 199 (apoC-I(7-24)) and 266 (apoC-I(35-53)) distance restraints were used, in distance geometry and simulated annealing calculations to generate, average structures for both peptides in aqueous solutions containing SDS., The backbone (N, C alpha, C = O) RMSD from the average structure of an, ensemble of 20 structures was 0.73 +/- 0.22 and 0.48 +/- 0.14 A for, apoC-I(7-24) and apoC-I(35-53), respectively. In the presence of SDS, the, distance geometry and simulated annealing calculations show that both, peptides adopt well-defined amphipathic helices with distinct hydrophobic, and hydrophilic faces. The calculated structures are discussed relative to, predicted structures. Comparing our CD and NMR results for the apoC-I, fragments in SDS with CD results of others obtained in the presence of, dimyristoylphosphatidylcholine indicates that SDS may be a better model of, the lipoprotein environment.
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Peptides corresponding to the proposed lipid-binding domains of human apolipoprotein C-I, residues 7-24 (ALDKLKEFGNTLEDKARE) and 35-53 (SAKMREWFSETFQKVKEKL), were studied by CD and two-dimensional 1H NMR spectroscopy. Sodium dodecyl sulfate (SDS) was used to model the lipoprotein environment. Analysis of the CD data shows that both peptides lack well-defined structure in aqueous solution but adopt helical, ordered structures upon the addition of SDS. The helical nature of the peptides in the presence of SDS was confirmed by H alpha secondary shifts. A total of 199 (apoC-I(7-24)) and 266 (apoC-I(35-53)) distance restraints were used in distance geometry and simulated annealing calculations to generate average structures for both peptides in aqueous solutions containing SDS. The backbone (N, C alpha, C = O) RMSD from the average structure of an ensemble of 20 structures was 0.73 +/- 0.22 and 0.48 +/- 0.14 A for apoC-I(7-24) and apoC-I(35-53), respectively. In the presence of SDS, the distance geometry and simulated annealing calculations show that both peptides adopt well-defined amphipathic helices with distinct hydrophobic and hydrophilic faces. The calculated structures are discussed relative to predicted structures. Comparing our CD and NMR results for the apoC-I fragments in SDS with CD results of others obtained in the presence of dimyristoylphosphatidylcholine indicates that SDS may be a better model of the lipoprotein environment.
==About this Structure==
==About this Structure==
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[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: Buchko, G.W.]]
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[[Category: Buchko, G W.]]
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[[Category: Cushley, R.J.]]
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[[Category: Cushley, R J.]]
[[Category: Rozek, A.]]
[[Category: Rozek, A.]]
[[Category: apolipoprotein]]
[[Category: apolipoprotein]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri Feb 15 15:29:14 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 11:45:49 2008''

Revision as of 09:45, 21 February 2008


1ale

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CONFORMATION OF TWO PEPTIDES CORRESPONDING TO HUMAN APOLIPOPROTEIN C-I RESIDUES 7-24 AND 35-53 IN THE PRESENCE OF SODIUM DODECYLSULFATE BY CD AND NMR SPECTROSCOPY

Overview

Peptides corresponding to the proposed lipid-binding domains of human apolipoprotein C-I, residues 7-24 (ALDKLKEFGNTLEDKARE) and 35-53 (SAKMREWFSETFQKVKEKL), were studied by CD and two-dimensional 1H NMR spectroscopy. Sodium dodecyl sulfate (SDS) was used to model the lipoprotein environment. Analysis of the CD data shows that both peptides lack well-defined structure in aqueous solution but adopt helical, ordered structures upon the addition of SDS. The helical nature of the peptides in the presence of SDS was confirmed by H alpha secondary shifts. A total of 199 (apoC-I(7-24)) and 266 (apoC-I(35-53)) distance restraints were used in distance geometry and simulated annealing calculations to generate average structures for both peptides in aqueous solutions containing SDS. The backbone (N, C alpha, C = O) RMSD from the average structure of an ensemble of 20 structures was 0.73 +/- 0.22 and 0.48 +/- 0.14 A for apoC-I(7-24) and apoC-I(35-53), respectively. In the presence of SDS, the distance geometry and simulated annealing calculations show that both peptides adopt well-defined amphipathic helices with distinct hydrophobic and hydrophilic faces. The calculated structures are discussed relative to predicted structures. Comparing our CD and NMR results for the apoC-I fragments in SDS with CD results of others obtained in the presence of dimyristoylphosphatidylcholine indicates that SDS may be a better model of the lipoprotein environment.

About this Structure

1ALE is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Conformation of two peptides corresponding to human apolipoprotein C-I residues 7-24 and 35-53 in the presence of sodium dodecyl sulfate by CD and NMR spectroscopy., Rozek A, Buchko GW, Cushley RJ, Biochemistry. 1995 Jun 6;34(22):7401-8. PMID:7779782

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