1993
DOI: 10.1002/pro.5560020105
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Disulfide bonding patterns and protein topologies

Abstract: This paper examines the topological properties of protein disulfide bonding patterns. First, a description of these patterns in terms of partially directed graphs is developed. The topologically distinct disulfide bonding patterns available to a polypeptide chain containing n disulfide bonds are enumerated, and their symmetry and reducibility properties are examined. The theoretical probabilities are calculated that a randomly chosen pattern of n bonds will have any combination of symmetry and reducibility pro… Show more

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Cited by 56 publications
(50 citation statements)
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“…The connectivity identification will be specifically addressed for peptides bearing six cysteines where three disulfide bonds can be formed. The number of possible disulfide isomers is described by the combinatorial formula [33] [Equation 4 where P(n) is the number of possible isomers and n the number of disulfide bonds considered]. The potential cysteine connectivities increase from 3 (for two disulfides) to 15 for three disulfides.…”
Section: Discussionmentioning
confidence: 99%
“…The connectivity identification will be specifically addressed for peptides bearing six cysteines where three disulfide bonds can be formed. The number of possible disulfide isomers is described by the combinatorial formula [33] [Equation 4 where P(n) is the number of possible isomers and n the number of disulfide bonds considered]. The potential cysteine connectivities increase from 3 (for two disulfides) to 15 for three disulfides.…”
Section: Discussionmentioning
confidence: 99%
“…Nevertheless, the results of this study show that the combined use of Fmoc-chemistry for the Noprotection (Fields & Noble, 1990) and of uronium salts (HBTU) for the activation of the carboxyl group (Knorr et al, 1989) can provide a successful synthesis of the 39-residue polypeptide chain of decorsin. In addition, the synthesis of this protein containing three disulfide bonds was expected to be difficult, both for an efficient and reversible protection of -SH groups during the synthesis, as well as for the correct pairing of disulfide bonds during the oxidative re-folding process of the reduced, synthetic polypeptide, because the six cysteine residues can form 15 different disulfidecrosslinked species (Creighton, 1984a;Benham & Jafri, 1993). On the other hand, the oxidative re-folding process of a reduced synthetic polypeptide to the native disulfide-crosslinked species leads to the formation of a globular entity with most of its hydrophobic groups buried in the protein interior and thus showing a lower affinity than the open chain polypeptide or mi-sfolded species for the hydrophobic matrix of the C18 column in RP-HPLC (Kent, 1988;Woo et al, 1989).…”
Section: Discussionmentioning
confidence: 99%
“…there are 105 possible combinations (P) of four disulfide bonds that can be formed (37). In cases where there is only one combination that is native and active, production, either in a recombinant sense or by solid phase peptide synthesis, often results in a complex mixture of misfolded isomers that need to be separated from the native isomer of interest.…”
Section: Improving Chemical and Physical Stabilitymentioning
confidence: 99%