Cited by 485Polymer Surface Interaction StudiesBiochemical and Structural CharacterizationMarine Biology and Environmental Chemistry

The DOI matches its Crossref record; 9 of the 9 references it cites were found in a registry or an index.

Cross-Linking in Adhesive Quinoproteins: Studies with Model Decapeptides

Burzio, Luis A., Waite, J. Herbert·2000·Biochemistry

DOI 10.1021/bi0002434

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Abstract

Mytilus edulis foot protein-1 (mefp1) is a major component of the byssus, an adhesive holdfast in mussels. The recent report of 5, 5'-di(dihydroxyphenyl-L-alanine) (diDOPA) cross-links in byssus [McDowell et al. (1999) J. Biol. Chem. 274, 20293] has raised questions about the relationship of these to mefp1. About 80% of the primary structure of mefp1 consists of a tandemly repeated consensus sequence Ala(1)-Lys(2)-Pro(3)-Ser(4)-Tyr(5)-Pro(6)-Pro(7)-Thr(8)-Tyr(9)-Lys(10 ) with varying degrees of posttranslational hydroxylation to hydroxyprolines in positions 3, 6, and 7 and to DOPA in positions 5 and 9. Six natural or synthetic variants of this decapeptide were subjected to oxidation by tyrosinase or periodate. DOPA is the only residue to suffer losses in all oxidized peptides. Moreover, using MALDI TOF mass spectrometry, oxidized decapeptides all showed evidence of multimer formation and a mass loss of 6 Da per coupled pair of peptides. Multimer formation was inhibited by addition of DOPA-like o-diphenols, but addition of simple amines such as free Lys had no effect. The results are consistent with aryloxy coupling to diDOPA followed by reoxidation to diDOPA quinone. There are subtle but noteworthy variations, however, in multimer formation among the peptide congeners. Decapeptides with Pro(3) modified to trans-4-hydroxyproline do not form multimers beyond dimers; they also exhibit significant Lys losses following oxidation of DOPA. Moreover, in Ala-Lys-Hyp-Ser-Tyr-DiHyp-Hyp-…

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Oxidative coupling of phenols
Dewar, M. J. S., & Nakaya, T. (1968) · Journal of the American Chemical Society · doi:10.1021/ja01027a051 · Cited by 556
Rotational Echo Double Resonance Detection of Cross-links Formed in Mussel Byssus under High-Flow Stress
McDowell, L. M., Burzio, L. A., Waite, J. H., & Schaefer, J. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.29.20293 · Cited by 181
Self-citation
Optimization of hydroxylation of tyrosine and tyrosine-containing peptides by mushroom tyrosinase
Marumo, K., & Waite, J. H. (1986) · Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology · doi:10.1016/0167-4838(86)90152-4 · Cited by 159
Self-citation
A Rapid Vapor-Phase Acid (Hydrochloric Acid and Trifluoroacetic Acid) Hydrolysis of Peptide and Protein
Tsugita, A., Uchida, T., Mewes, H., & Ataka, T. (1987) · The Journal of Biochemistry · doi:10.1093/oxfordjournals.jbchem.a122209 · Cited by 124
Unimolecular micelles: Synthesis and characterization of amphiphilic polymer systems
Liu, H., Jiang, A., Guo, J. W., & Uhrich, K. E. (1999) · Journal of Polymer Science Part A Polymer Chemistry · doi:10.1002/(sici)1099-0518(19990315)37:6 · Cited by 105
Some observations on the reaction of catechol derivatives with amines and amino acids in presence of oxidizing agents
Hackman, R. H., & Todd, A. R. (1953) · Biochemical Journal · doi:10.1042/bj0550631 · Cited by 70
Phenoloxidase catalyzed coupling of catechols. Identification of novel coupling products
ANDERSEN, S. O., Jacobsen, J. P., Bojesen, G., & Roepstorff, P. (1992) · Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology · doi:10.1016/0167-4838(92)90140-9 · Cited by 39
Matrix-Assisted Laser Desorption/Ionization Time-of-Flight
Bryson, A. L., Hill, E. M., & Doern, C. D. (2019) · Clinics in Laboratory Medicine · doi:10.1016/j.cll.2019.05.010 · Cited by 27
Adhesion in Cellulosic and Wood-Based Composites
(1981) · Springer eBooks · doi:10.1007/978-1-4684-8983-5 · Cited by 17

Show all 9 references

Research works printed but not linked: 25

Bell E. C., 1997, Mar. Biol. Ecol. Prog. Ser. 159, 197−208
Deming T. J., 1999, Curr. Opin. Chem. Biol. 3, 100−105
Waite J. H., 1997, J. Adhes. Soc. Jpn., 33
Deacon M. P., 1998, Biochemistry 37, 14108−14112
Taylor S. W., 1994, J. Am. Chem. Soc., 116
Laursen R., 1992, Results Probl. Cell Differ., 19, 72
Filpula D. R., 1990, Biotechnol. Prog. 6, 171−177
Hansen D. C., 1998, Langmuir 14, 743−746
Yamamoto H., 1995, J. Mar. Biotechnol., 2, 100
Burzio, L. A. (1999) Ph.D. Thesis, University of Delaware, Newark, DE.
Waite J. H., 1995, Methods Enzymol., 258, 19
Sizer I., 1953, Adv. Enzymol. 14, 129−171
Mason H. S., 1948, J. Biol. Chem., 172, 99
Mason H. S., 1955, Biochim. Biophys. Acta, 111
Xu R., 1997, Insect Biochem. Mol. Biol. 27, 101−108
Wang S. X., 1996, Science 273, 1078−1084
Holl S. M., 1993, Arch. Biochem. Biophys. 302, 255−258
Klug C. A., 1996, Arch. Biochem. Biophys. 333, 221−224
Michon T., 1997, Biopolymers 36, 8504−8513
Zimmermann W., 1989, Chimia 43, 396−403
Wilmot C. M., 1999, Science 286, 1724−1728
Benavente M. G., 1991, Arch. Biochem. Biophys. 290, 451−457
Mason H. S., 1961, Biochem. Biophys. Res. Commun. 4, 236−238
Koga S., 1992, Arch. Biochem. Biophys. 292, 570−575
Waite J. H., 1976, Anal. Biochem. 75, 211−218

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Microwave‐Accelerated Rapid, Chemical Oxidant‐Free, Material‐Independent Surface Chemistry of Poly(dopamine)
Lee, M., Lee, S. T., Oh, I., & Lee, H. (2016) · Small · doi:10.1002/smll.201600443 · Cited by 119
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Liu, G., Jiang, Z., Chen, C., Hou, L., Gao, B., Yang, H., Wu, H., Pan, F., Zhang, P., & Cao, X. (2017) · Journal of Membrane Science · doi:10.1016/j.memsci.2017.05.025 · Cited by 112
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Authors: Burzio, L. A., & Waite, J. H.
Affiliations: University of California, Santa Barbara (US)
ORCID: Waite, J. Herbert
Venue: Biochemistry
Publisher: American Chemical Society (ACS)
Published: 2000-08-17
Volume: 39
Issue: 36
Pages: 11147-11153
ISSN: 0006-2960 (ISSN-L)
1520-4995
DOI: 10.1021/bi0002434
OpenAlex: W2011121154
Cited by: 485
References: 9
Citations by year: 2026: 4 · 2025: 9 · 2024: 18 · 2023: 19 · 2022: 23 · 2021: 37 · 2020: 25 · 2019: 29 · 2018: 28 · 2017: 34 · 2016: 37 · 2015: 24 · 2014: 28 · 2013: 19 · 2012: 24
FWCI: 6.45
Type: journal article
Language: en
Open access: closed
Locations: Biochemistry (publishedVersion)
PubMed (publishedVersion)
Funders: National Institutes of Health (5r01de010042-11)
National Institute of Dental and Craniofacial Research (DE10042)
Topics: Physical Sciences › Materials Science › Surfaces, Coatings and Films › Polymer Surface Interaction Studies
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Biochemical and Structural Characterization
Physical Sciences › Engineering › Ocean Engineering › Marine Biology and Environmental Chemistry
Keywords: byssus, DOPA oxidation, periodate oxidation, hydroxyproline, trans-4-hydroxyproline, o-diphenols
MeSH terms: Adhesiveness, Adhesives, Animals, Cross-Linking Reagents, Dihydroxyphenylalanine, Glycine, Hydrolysis, Lysine, Models, Molecular, Oligopeptides, Oxidation-Reduction, Proteins, Quinones, Spectrophotometry, Ultraviolet, Tyrosine, Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization, Bivalvia

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Cross-Linking in Adhesive Quinoproteins: Studies with Model Decapeptides

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