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Journal Abstract Search

194 related items for PubMed ID: 8619475

  • 1. Formation of N-substituted 2-iminothiolanes when amino groups in proteins and peptides are modified by 2-iminothiolane.
    Singh R, Kats L, Blättler WA, Lambert JM.
    Anal Biochem; 1996 Apr 05; 236(1):114-25. PubMed ID: 8619475
    [Abstract] [Full Text] [Related]

  • 2. Liquid secondary ion mass spectra of 2-iminothiolane derivatives.
    Bartlett MG, Busch KL.
    Biol Mass Spectrom; 1994 Jun 05; 23(6):353-6. PubMed ID: 8038228
    [Abstract] [Full Text] [Related]

  • 3. Nuclear magnetic resonance studies on covalent modification of amino acids thiol and amino residues by monofunctional aryl 13C-isocyanates, models of skin and respiratory sensitizers: transformation of thiocarbamates into urea adducts.
    Fleischel O, Giménez-Arnau E, Lepoittevin JP.
    Chem Res Toxicol; 2009 Jun 05; 22(6):1106-15. PubMed ID: 19405514
    [Abstract] [Full Text] [Related]

  • 4. Evidence for the formation of adducts and S-(carboxymethyl)cysteine on reaction of alpha-dicarbonyl compounds with thiol groups on amino acids, peptides, and proteins.
    Zeng J, Davies MJ.
    Chem Res Toxicol; 2005 Aug 05; 18(8):1232-41. PubMed ID: 16097796
    [Abstract] [Full Text] [Related]

  • 5. Effects of buried charged groups on cysteine thiol ionization and reactivity in Escherichia coli thioredoxin: structural and functional characterization of mutants of Asp 26 and Lys 57.
    Dyson HJ, Jeng MF, Tennant LL, Slaby I, Lindell M, Cui DS, Kuprin S, Holmgren A.
    Biochemistry; 1997 Mar 04; 36(9):2622-36. PubMed ID: 9054569
    [Abstract] [Full Text] [Related]

  • 6. Structure of subtilosin A, a cyclic antimicrobial peptide from Bacillus subtilis with unusual sulfur to alpha-carbon cross-links: formation and reduction of alpha-thio-alpha-amino acid derivatives.
    Kawulka KE, Sprules T, Diaper CM, Whittal RM, McKay RT, Mercier P, Zuber P, Vederas JC.
    Biochemistry; 2004 Mar 30; 43(12):3385-95. PubMed ID: 15035610
    [Abstract] [Full Text] [Related]

  • 7. Caution in the use of 2-iminothiolane (Traut's reagent) as a cross-linking agent for peptides. The formation of N-peptidyl-2-iminothiolanes with bombesin (BN) antagonist (D-Trp(6),Leu(13)-psi[CH(2)NH]-Phe(14))BN(6-14) and D-Trp-Gln-Trp-NH(2).
    Mokotoff M, Mocarski YM, Gentsch BL, Miller MR, Zhou JH, Chen J, Ball ED.
    J Pept Res; 2001 May 30; 57(5):383-9. PubMed ID: 11350598
    [Abstract] [Full Text] [Related]

  • 8. Systematic characterization of the covalent interactions between (-)-epigallocatechin gallate and peptides under physiological conditions by mass spectrometry.
    Cao D, Zhang Y, Zhang H, Zhong L, Qian X.
    Rapid Commun Mass Spectrom; 2009 Apr 30; 23(8):1147-57. PubMed ID: 19280611
    [Abstract] [Full Text] [Related]

  • 9. Thiolation of chitosan. Attachment of proteins via thioether formation.
    Masuko T, Minami A, Iwasaki N, Majima T, Nishimura S, Lee YC.
    Biomacromolecules; 2005 Apr 30; 6(2):880-4. PubMed ID: 15762654
    [Abstract] [Full Text] [Related]

  • 10. Substituted 2-iminothiolanes: reagents for the preparation of disulfide cross-linked conjugates with increased stability.
    Goff DA, Carroll SF.
    Bioconjug Chem; 1990 Apr 30; 1(6):381-6. PubMed ID: 2099186
    [Abstract] [Full Text] [Related]

  • 11. Protein and low molecular mass thiols as targets and inhibitors of glycation reactions.
    Zeng J, Davies MJ.
    Chem Res Toxicol; 2006 Dec 30; 19(12):1668-76. PubMed ID: 17173381
    [Abstract] [Full Text] [Related]

  • 12. Chemical cross-linking with NHS esters: a systematic study on amino acid reactivities.
    Mädler S, Bich C, Touboul D, Zenobi R.
    J Mass Spectrom; 2009 May 30; 44(5):694-706. PubMed ID: 19132714
    [Abstract] [Full Text] [Related]

  • 13. Covalent modification of lysine residues by allyl isothiocyanate in physiological conditions: plausible transformation of isothiocyanate from thiol to amine.
    Nakamura T, Kawai Y, Kitamoto N, Osawa T, Kato Y.
    Chem Res Toxicol; 2009 Mar 16; 22(3):536-42. PubMed ID: 19216492
    [Abstract] [Full Text] [Related]

  • 14. A cleavable amino-thiol linker for reversible linking of amines to DNA.
    Højfeldt JW, Blakskjaer P, Gothelf KV.
    J Org Chem; 2006 Dec 08; 71(25):9556-9. PubMed ID: 17137397
    [Abstract] [Full Text] [Related]

  • 15. Model studies on protein side chain modification by 4-oxo-2-nonenal.
    Zhang WH, Liu J, Xu G, Yuan Q, Sayre LM.
    Chem Res Toxicol; 2003 Apr 08; 16(4):512-23. PubMed ID: 12703968
    [Abstract] [Full Text] [Related]

  • 16. Partial acetylation of lysine residues improves intraprotein cross-linking.
    Guo X, Bandyopadhyay P, Schilling B, Young MM, Fujii N, Aynechi T, Guy RK, Kuntz ID, Gibson BW.
    Anal Chem; 2008 Feb 15; 80(4):951-60. PubMed ID: 18201069
    [Abstract] [Full Text] [Related]

  • 17. Thiol-modified chitosan sulfate nanoparticles for protection and release of basic fibroblast growth factor.
    Ho YC, Wu SJ, Mi FL, Chiu YL, Yu SH, Panda N, Sung HW.
    Bioconjug Chem; 2010 Jan 15; 21(1):28-38. PubMed ID: 20000719
    [Abstract] [Full Text] [Related]

  • 18. Novel amidinating cross-linker for facilitating analyses of protein structures and interactions.
    Lauber MA, Reilly JP.
    Anal Chem; 2010 Sep 15; 82(18):7736-43. PubMed ID: 20795639
    [Abstract] [Full Text] [Related]

  • 19. Derivatization procedures to facilitate de novo sequencing of lysine-terminated tryptic peptides using postsource decay matrix-assisted laser desorption/ionization mass spectrometry.
    Keough T, Lacey MP, Youngquist RS.
    Rapid Commun Mass Spectrom; 2000 Sep 15; 14(24):2348-56. PubMed ID: 11114049
    [Abstract] [Full Text] [Related]

  • 20. Orientation of the crotonaldehyde-derived N2-[3-Oxo-1(S)-methyl-propyl]-dG DNA adduct hinders interstrand cross-link formation in the 5'-CpG-3' sequence.
    Cho YJ, Wang H, Kozekov ID, Kozekova A, Kurtz AJ, Jacob J, Voehler M, Smith J, Harris TM, Rizzo CJ, Lloyd RS, Stone MP.
    Chem Res Toxicol; 2006 Aug 15; 19(8):1019-29. PubMed ID: 16918240
    [Abstract] [Full Text] [Related]

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