Structural studies of collagen-like sequential polypeptides

Heidemann, E.; Neiss, H. G.; Khodadadeh, Keyumarss; Heymer, G.; Sheikh, E.M. El; Saygin, Oe.

doi:10.1016/0032-3861(77)90155-0

Cited by 8 publications

(1 citation statement)

References 10 publications

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“…Heidemann used propane tricarboxylate tris(pentachlorophenyl) and N-tris(6-amino hexanoyl)-lysyllysine as covalent bridging molecules for the three chains [39]. Other covalent linkers include Kemp triacid [40], a modified dilysine system [41], the sequence found at the C-terminal end of type III collagen Gly-Pro-Cys-Cys-Gly [42][43][44][45][46], and tris(2-aminoethyl)amine with succinic acid spacers [47].…”

Section: Type Of Peptidesmentioning

confidence: 99%

The Thermodynamics and Kinetics of Collagen Folding

Bächinger¹,

Engel²

2005

Protein Folding Handbook

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Section: Type Of Peptidesmentioning

confidence: 99%

The Thermodynamics and Kinetics of Collagen Folding

Bächinger¹,

Engel²

2005

Protein Folding Handbook

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Investigation on polyethylene films of controllable service life

Bálint

Halász

Iring

et al. 1983

Angew. Makromol. Chem.

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The effect of a special additive containing stabilizer and sensitizer groups was studied in thermal and photooxidation of polypropylene. In thermooxidation, the induction period of oxygenz absorption decreased, and its rate increased with the increase of the amount of the additive. In photooxidation, however, the shortest induction period and highest rate of carbonyl formation can be achieved at an optimal additive concentration.The final molecular mass of the samples after irradiation till the spontaneous rupture falls in the range of moldecular mass consumable for the microbes. On the basis of the results, it seems to be possible to stabilize the polymer during processing and storage, and sensitize under solar irradiation with the same additive.Paper presented a t t h e

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Properties of thermoreversible gels

Borchard¹

1998

Ber Bunsenges Phys Chem

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In a short survey chemical and physical aspects characterising thermoreversibly gelling systems are gathered. Rheological properties of the system gelatin/water for different polymer concentrations at various temperatures and varying angular frequencies are presented. The results are interpreted following the percolation theory. The relevant exponents of the storage and loss modulus are close to the percolation model of Arbabi and Sahimi. The pre‐gel properties favour the Zimm‐limit whereas the post‐gel properties are close to the Rouse‐limit. This controversial behaviour is discussed. The gel‐point has been determined by the divergence criterion of the dynamic viscosity at zero frequency when the storage modulus vanishes. The critical times in the percolation results agree fairly well with the time of gelation but not with the cross over time of the storage and loss modulus curves versus time at zero frequency. An equilibrium aggregation model for the post gelation processes is presented which is based on the percolation approach. The time dependence of the storage modulus can be described in the total time range between gel point and the final equilibrium value after very long times.

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Structural studies of collagen-like sequential polypeptides

Cited by 8 publications

References 10 publications

The Thermodynamics and Kinetics of Collagen Folding

The Thermodynamics and Kinetics of Collagen Folding

Investigation on polyethylene films of controllable service life

Properties of thermoreversible gels

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