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Buchumschlag von Conformational analysis of a IgG1 hinge peptide derivative in solution determined by NMR spectroscopy and refined by restrained molecular dynamics simulations
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Conformational analysis of a IgG1 hinge peptide derivative in solution determined by NMR spectroscopy and refined by restrained molecular dynamics simulations

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Zeitschriftentitel: Biopolymers
Personen und Körperschaften: Kessler, Horst, Mronga, Siggi, Müller, Gerhard, Moroder, Luis, Huber, Robert
In: Biopolymers, 31, 1991, 10, S. 1189-1204
Medientyp: E-Article
Sprache: Englisch
veröffentlicht:
Wiley
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Zusammenfassung: <jats:title>Abstract</jats:title><jats:p>The hinge region links the antigen binding F<jats:sub>ab</jats:sub> part to the constant F<jats:sub>c</jats:sub> domain in immunoglobulins. For the hinge peptide derivative [AcThr(OtBu)‐Cys‐Pro‐Pro‐Cys‐Pro‐Ala‐ProNH<jats:sub>2</jats:sub>]<jats:sub>2</jats:sub> the assignment of the <jats:sup>1</jats:sup>H and <jats:sup>13</jats:sup>C resonances was achieved by two‐dimensional nmr techniques: total correlation spectroscopy (TOCSY), nuclear Ovethauser enhancement spectroscopy (NOESY), rotating frame nuclear Overhauser enhancement spectroscopy (ROESY), heteronuclear multiple quantum coherence (HMQC) transfer, and a HSQC (modified Overbodenhausen experiment) with high resolution in F<jats:sub>1</jats:sub>, which was several times folded in F<jats:sub>1</jats:sub> but still phase correctable. Conformational relevant parameters (78 nuclear Overhauser effect distance restraints, <jats:sup>3</jats:sup><jats:italic>J</jats:italic><jats:sub>HH</jats:sub> for prochiral assignments, temperature gradients) were determined by nmr and served as input data for molecular dynamics (MD) structure refinement. A simulated model compound corresponding to the [Cys‐Pro‐Pro‐Cys]<jats:sub>2</jats:sub> core elongated by the peptide chains in the F<jats:sub>ab</jats:sub> and F<jats:sub>c</jats:sub> direction served as a starting structure for the final MD run. The conformation calculated in <jats:italic>in vacuo</jats:italic> does not agree with the C<jats:sub>2</jats:sub> symmetry required from nmr data, but the structure obtained by a water simulation fulfills the requirement. Here the core of the hinge peptide derivative adopts a polyproline II double helix as in the x‐ray structure of IgG1. Hence, segments responsible for the internal flexibility are located outside the core as confirmed by the flexibility of the solvent exposed C termini.</jats:p>
Umfang: 1189-1204
ISSN: 1097-0282
0006-3525
DOI: 10.1002/bip.360311007