Results 11 to 20 of about 39,961 (248)

Melanization and Tyrosinase Activity

open access: yesJournal of Investigative Dermatology, 1971
Purified soluble tyrosinase isolated from the melanosomes of Harding-Passey mouse melanoma was incubated with L-dopa. The reaction velocity of the tyrosinase thus incubated decreased significantly. There was an inverse linear relationship between the concentration of dopa in the preincubation mixture and the reaction velocity of the tyrosinase which ...
Seiji, Makoto, Miyazaki, Kazuhiro
openaire   +3 more sources

Tyrosinase-Mediated Synthesis of Nanobody–Cell Conjugates

open access: yes, 2022
A convenient enzymatic strategy is reported for the modification of cell surfaces. Using a tyrosinase enzyme isolated from Agaricus bisporus, unique tyrosine residues introduced at the C-termini of nanobodies can be site-selectively oxidized to reactive ...
Daniel K. Nomura (198023)   +5 more
core   +3 more sources

Tyrosinase-Based Proximity Labeling in Living Cells and In Vivo

open access: yes
Characterizing the protein constituents of a specific organelle and protein neighbors of a protein of interest (POI) is essential for understanding the function and state of the organelle and protein networks associated with the POI.
Hao Zhu (56502)   +8 more
core   +8 more sources

Experimental Evidence and Mechanistic Description of the Phenolic H‑Transfer to the Cu2O2 Active Site of oxy-Tyrosinase

open access: yes, 2023
Tyrosinase is a ubiquitous coupled binuclear copper enzyme that activates O2 toward the regioselective monooxygenation of monophenols to catechols via a mechanism that remains only partially defined.
Martin Srnec (1263150)   +6 more
core   +2 more sources

Tyrosinase-Catalyzed Peptide Macrocyclization for mRNA Display

open access: yes, 2023
mRNA display of macrocyclic peptides has proven itself to be a powerful technique to discover high-affinity ligands for a protein target. However, only a limited number of cyclization chemistries are known to be compatible with mRNA display.
Albert A. Bowers   +9 more
core   +1 more source

Crystal Structure of Agaricus bisporus Mushroom Tyrosinase: Identity of the Tetramer Subunits and Interaction with Tropolone [PDF]

open access: yes, 2011
Tyrosinase catalyzes the conversion of phenolic compounds into their quinone derivatives, which are precursors for the formation of melanin, a ubiquitous pigment in living organisms.
Dijkstra, B.W.   +28 more
core   +1 more source

Structure and Function of Human Tyrosinase and Tyrosinase‐Related Proteins [PDF]

open access: yesChemistry – A European Journal, 2017
AbstractMelanin is the main pigment responsible for the color of human skin, hair and eye. Its biosynthesis requires three melanogenic enzymes, tyrosinase (TYR), and the tyrosinase‐related proteins TYRP1 and TYRP2. The difficulty of isolating pure and homogeneous proteins from endogenous sources has hampered their study, and resulted in many ...
Xuelei Lai   +3 more
openaire   +3 more sources

In vitro and in silico insights into tyrosinase inhibitors with (E)-benzylidene-1-indanone derivatives

open access: yesComputational and Structural Biotechnology Journal, 2019
Tyrosinase is a key enzyme responsible for melanin biosynthesis and is effective in protecting skin damage caused by ultraviolet radiation. As part of ongoing efforts to discover potent tyrosinase inhibitors, we systematically designed and synthesized ...
Hee Jin Jung   +6 more
doaj   +1 more source

Phlorotannins Derived From the Brown Alga as Tyrosinase Inhibitors

open access: yesNatural Product Communications, 2021
Tyrosinase catalyzes hydroxylation of L-tyrosine and dehydrogenation of L-DOPA in the melanin biosynthesis pathway. Tyrosinase inhibitors have potential use as cosmetic whitening agents and for preventing seafood deterioration. In this report, tyrosinase
Hideyuki Kurihara, Kazuki Kujira
doaj   +1 more source

A Potent Tyrosinase Inhibitor, (E)-3-(2,4-Dihydroxyphenyl)-1-(thiophen-2-yl)prop-2-en-1-one, with Anti-Melanogenesis Properties in α-MSH and IBMX-Induced B16F10 Melanoma Cells

open access: yesMolecules, 2018
In this study, we designed and synthesized eight thiophene chalcone derivatives (1a–h) as tyrosinase inhibitors and evaluated their mushroom tyrosinase inhibitory activities.
Chang Seok Kim   +7 more
doaj   +1 more source

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