Development of an automated protein-tyrosine phosphatase 1B inhibition assay and the screening of putative insulin-enhancing vanadium(IV) and zinc(II) complexes.

Abstract:

:The inhibition of protein-tyrosine phosphatase 1B (PTP1B) is a potential target for treatment of type 2 diabetes. Vanadium and zinc metal coordinated complexes have insulin-enhancing activities, and while vanadium compounds inhibit PTP1B, little is known on the mode of action of zinc compounds. In this study we developed an automated PTP1B inhibition assay that allows for a rapid assessment of the PTP1B inhibition strength of candidate compounds. Synthetic vanadium(IV) and zinc(II) complexes were evaluated: IC50 values for vanadium complexes ranged from 0.06 to 0.8 microM whereas for zinc compounds, values were above 10 microM. Vanadium sulfate, a non-conjugated inorganic salt, had stronger inhibition activity than any of the conjugated metal complexes.

journal_name

Biotechnol Lett

journal_title

Biotechnology letters

authors

Seale AP,de Jesus LA,Kim SY,Choi YH,Lim HB,Hwang CS,Kim YS

doi

10.1007/s10529-004-7855-8

keywords:

subject

Has Abstract

pub_date

2005-02-01 00:00:00

pages

221-5

issue

4

eissn

0141-5492

issn

1573-6776

journal_volume

27

pub_type

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