Unknown

Dataset Information

0

A facile and versatile methodology for cysteine specific labeling of proteins with octahedral polypyridyl d? metal complexes.


ABSTRACT: We have synthesized and characterized four octahedral polypyridyl d(6) metal complexes bearing the 5,6-epoxy-5,6-dihydro-[1,10]phenanthroline ligand (L1) as cysteine specific labeling reagents. The proposed synthetic pathways allow the preparation of the metal complexes containing Re(I), Ru(II), Os(II) and Ir(III) while preserving the epoxide functionality. The complexes were characterized by (1)H and (13)C NMR, mass spectrometry, UV-visible and luminescence spectroscopies as well as cyclic voltammetry. As proof of concept, a set of non-native single cysteine P450 BM3 heme domain mutants previously developed in our laboratory was used to study the labeling reaction. We demonstrate that the proposed labels can selectively react, often in high yield, with cysteine residues of the protein via the nucleophilic thiol ring opening of the epoxide moiety. In addition, under basic conditions, subsequent loss of a water molecule led to the aromatization of the phenanthroline ring on the protein-bound label compounds, as observed by mass spectrometry and luminescence measurements.

SUBMITTER: Dwaraknath S 

PROVIDER: S-EPMC4058400 | biostudies-literature | 2014 Jul

REPOSITORIES: biostudies-literature

altmetric image

Publications

A facile and versatile methodology for cysteine specific labeling of proteins with octahedral polypyridyl d⁶ metal complexes.

Dwaraknath Sudharsan S   Tran Ngoc-Han NH   Dao Thanh T   Colbert Alexander A   Mullen Sarah S   Nguyen Angelina A   Cortez Alejandro A   Cheruzel Lionel L  

Journal of inorganic biochemistry 20140110


We have synthesized and characterized four octahedral polypyridyl d(6) metal complexes bearing the 5,6-epoxy-5,6-dihydro-[1,10]phenanthroline ligand (L1) as cysteine specific labeling reagents. The proposed synthetic pathways allow the preparation of the metal complexes containing Re(I), Ru(II), Os(II) and Ir(III) while preserving the epoxide functionality. The complexes were characterized by (1)H and (13)C NMR, mass spectrometry, UV-visible and luminescence spectroscopies as well as cyclic volt  ...[more]

Similar Datasets

| S-EPMC5410163 | biostudies-literature
| S-EPMC7547867 | biostudies-literature
| S-EPMC3076536 | biostudies-literature
| S-EPMC6899727 | biostudies-literature
| S-EPMC3665721 | biostudies-other
| S-EPMC2790122 | biostudies-literature
| S-EPMC5431136 | biostudies-literature
| S-EPMC5785092 | biostudies-literature
| S-EPMC3093568 | biostudies-literature
| S-EPMC4878437 | biostudies-literature