Sentence examples for disulfide molecules from inspiring English sources

Selenocystamine and cystamine, diselenide and disulfide molecules, respectively, were fed to Chlamydomonas reinhardtii cultures.

In this contribution, we explored the possibility of using selenol and selenide molecules to form self-assembled monolayers (SAMs) on copper, in order to check the influence of anchoring groups on SAMs quality and compared it to well-known thiolate assemblies (formed with thiol and disulfide molecules).

In the present study, for the purpose of establishment of a new robust basement for heterogeneous metal catalysts, a SAM of the alkanethiolate terminated with NHC rhodium(I) complex moiety was prepared by utilizing a newly designed disulfide molecule bearing NHC metal complex terminals.

α-Lipoic Acid is a naturally occurring disulfide molecule with antioxidant and anti-inflammatory properties.

Attempts to obtain the reduced form of Etrx2 by co-crystallization with β-mercaptoethanol resulted in a new oxidized structure in which Etrx2 forms a complex with a 2-hydroxyethyl disulfide (HED) molecule (Fig 4D).

Through the formation of the disulfide bonds, PFDT molecules are able to covalently bind onto the thiol-terminated silicon substrate as shown in Fig. 1.

In terms of protein responses, protein S-glutathionylation is a unique post-translational modification of protein reactive cysteines forming disulfides with glutathione molecules.

We considered it possible that the low abundance TatCHis species observed by BN-PAGE (Figs. 1 and 4B) corresponded to complexes containing the disulfide-linked TatCHis molecules.

This gene encodes uromodulin (the Tamm Horsfall glycoprotein), a disulfide bond-rich molecule that is normally the most abundant protein in human urine [ 30].

It is notable that the TatBCHis preparation does not contain disulfide-linked TatC molecules (Fig. 2B) suggesting that the TatB protomers shield the reactive TatC cysteine(s) to some extent.

The preserved disulfide bond spacer molecule is able to respond to the reducing reagents, such as high concentration glutathione (∼10 mM) within the tumor intracellular microenvironment, where photo de-cross-linking is not easily achievable because of poor penetration and cytotoxicity of UV light.