Asakawa D (2016) Principles of hydrogen radical mediated peptide/protein fragmentation during matrix- assisted laser desorption/ionization mass spectrometry. Mass Spectrom Rev 35:535–556
Article CAS PubMed Google Scholar
Asakawa D, Osaka I (2017) Direct MALDI-MS analysis of the disulfide bonds in peptide using thiosalicylic acid as a reactive matrix. J Mass Spectrom 52:127–131
Article CAS PubMed Google Scholar
Banerjee AK, Laya Mimó MS, Vera Vegas WJ (2001) Silica gel in organic synthesis. Russ Chem Rev 70(11):971–990
Buko AM, Fraser BA (1985) Peptide studies using a fast atom bombardment high field mass spectrometer and data system 4. Disulfide-containing peptides. Biomed Mass Spectrom 12(10):577–585
Article CAS PubMed Google Scholar
Choi JS, Joo SH (2020) Recent trends in cyclic peptides as therapeutic agents and biochemical tools. Biomol Ther 28:18–24
de Veer SJ, Kan MW, Craik DJ (2019) Cyclotides: from structure to function. Chem Rev 119:12375–12421
DiGiorno MC, Vithanage N, Victorio CG, Kreitler DF, Outlaw VK, Sawyer N (2024) Structural characterization of disulfide-linked p53-derived peptide dimers. Int J Pept Res Ther 30:68
Fag GM, Chen XX, Yang QQ, Zhu LJ, Li NN, Yu HZ, Meng XM (2018) Discovery, structure, and chemical synthesis of disulfide-rich peptide toxins and their analogs. Chin Chem Lett 29:1033–1042
Forte LR (2004) Guanylin. In: Johnson LR (ed) Encyclopedia of Gastroenterology. Elsevier USA, pp 262–264
Fujitake M, Harusawa S (2023) Accurate molecular weight measurements of cystine derivatives on FAB-MS. Bull Fac Pharm Osaka Med Pharm Univ 2:105–116. https://ompu.repo.nii.ac.jp/records/515
Fujitake M, Harusawa S, Araki L, Yamaguchi M, Lilley DMJ, Zhao Z, Kurihara T (2005) Accurate molecular weight measurements of nucleoside phosphoramidites: a suitable matrix of mass spectrometry. Tetrahedron 61:4689–4699
Gary S, Bloom S (2022) Peptide carbocycles: from – SS– to – CC– via a late-stage snip- and -stitch. ACS Cent Sci 8:1537–1547
Article CAS PubMed PubMed Central Google Scholar
Gimpl G, Fahrenholz F (2001) The oxytocin receptor system: structure, function, and regulation. Physiol Rev 81(2):629–683
Article CAS PubMed Google Scholar
Goto Y, Hamaguchi K (1979) The role of the intrachain disulfide bond in the conformation and stability of the constant fragment of the immunoglobulin light chain. J Biochem 86(5):1433–1441
Article CAS PubMed Google Scholar
Gross JH (2017) “Mass Spectrometry: A Text Book,” 3rd ed. Springer International Publishing AG
Guan X, Zhang L, Wypych J (2018) Direct mass spectrometric characterization of disulfide linkages. mAbs 10(4):572–582
Article CAS PubMed PubMed Central Google Scholar
Guo Y, Chen L, Yang L, Wang Q (2008) Counting sulfhydryls and disulfide bonds in peptides and proteins using mercurial ions as an MS-tag. J Am Soc Mass Spectrom 19:1108–1113
Article CAS PubMed Google Scholar
Haensele E, Mele N, Miljak M, Read CM, Whitley DC, Banting L, Delépée C, Oliveira Santos JS, Lepailleur A, Bureau R, Essex JW, Clark T (2017) Conformation and dynamics of human urotensin II and urotensin related peptide in aqueous solution. J Chem Inf Model 57:298–310
Article CAS PubMed Google Scholar
Hammer RP, Butrie MA, Davidson K, Goldblatt PT, Schrader AM, Dalluge JJ, Becker A, Barany G (2024) Scaled-up synthesis and characterization of oxytocin trisulfide. Int J Pept Res Ther 30(1):5
Jin AH, Muttenthaler M, Dutertre S, Himaya SWA, Kaas Q, Craik DJ, Lewis RJ, Alewood PF (2019) Conotoxins: chemistry and biology. Chem Rev 119:11510–11549
Article CAS PubMed Google Scholar
Johnson M, Liu M, Struble E, Hettiarachchi K (2015) Characterization of cyclic peptides containing disulfide bonds. J Pharm Biomed Anal 109:112–120
Article CAS PubMed PubMed Central Google Scholar
Joo SH (2012) Cyclic peptides as therapeutic agents and biochemical tools. Biomol Ther 20(1):19–26
Karas JA, Wade JD, Hossain MA (2021) The chemical synthesis of insulin: an enduring challenge. Chem Rev 121(8):4531–4560
Article CAS PubMed Google Scholar
Kotsuki H, Shimanouchi T, Ohshima R, Fujiwara S (1998) Tetrahedron 54:2709–2722
Kumar D, Kumar V, Salam A, Khan T (2019) A silica-gel accelerated [4 + 2] cycloaddition-based biomimetic approach towards the first total synthesis of magterpenoid C. Tetrahedron Lett 60:e151137
Lakbub JC, Shipman JT, Desaire H (2018) Recent mass spectrometry-based techniques and considerations for disulfide bond characterization in proteins. Anal Bioanal Chem 410:2467–2484
Article CAS PubMed Google Scholar
Li Y, Kolasinski KW, Zare RN (2023) Silica particles convert thiol-containing molecules to disulfides. PNAS 120(34):e2304735120
Article CAS PubMed PubMed Central Google Scholar
Lin J, Chen S, Butt UD, Yan M, Wu B (2024) A comprehensive review on ziconotide. Heliyon 10:e31105
Article CAS PubMed PubMed Central Google Scholar
Massonnet P, Haler JRN, Upert G, Smargiasso N, Mourier G, Gilles N, Quinton L, De Pauw E (2018) Disulfide connectivity analysis of peptides bearing two intramolecular disulfide bonds using MALDI in-source decay. J Am Soc Mass Spectrom 29:1995–2002
Article CAS PubMed Google Scholar
McAuley A, Jacob J, Kolvenbach CG, Westland K, Lee HJ, Brych SR, Rehder D, Kleemann GR, Brems DN, Matsumura M (2008) Contributions of a disulfide bond to the structure, stability, and dimerization of human IgG1 antibody CH3 domain. Protein Sci 17:95–106
Article CAS PubMed PubMed Central Google Scholar
Mohara S, Tanimoto M (1987) Reduction of disulfide-containing peptides in matrix on secondary ion mass spectrum measurement. Journal of the Mass Spectrometry Society of Japan 35(5):248–257
Muttenthaler M, Andersson A, de Araujo AD, Dekan Z, Lewis RJ, Alewood PF (2010) Modulating oxytocin activity and plasma stability by disulfide bond engineering. J Med Chem 53:8585–8596
Article CAS PubMed Google Scholar
Northfield SE, Wang CK, Schroeder CI, Durek T, Kan MW, Swedberg JE, Craik DJ (2014) Disulfide-rich macrocyclic peptides as templates in drug design. Eur J Med Chem 77:248–257
Article CAS PubMed Google Scholar
Onitsuka S, Jin YZ, Shaikh AC, Furuno H, Inanaga J (2012) Silica gel-mediated organic reactions under organic solvent-free conditions. Molecules 17:11469–11483
Comments (0)