Inhibition of creatine kinase by S‐nitrosoglutathione

FEBS Letters

Wolosker, Herman¹  Panizzutti, Rogério¹  Engelender, Simone¹ 

[1] Departamento de Bioquímica Médica, Instituto de Ciencias Biomédicas, Universidade Federal do Rio de Janeiro, Cidade Universitária, Rio de Janeiro, RJ 21910-590, Brazil

关键词: Nitric oxide;    Creatine kinase;    Ca2+-ATPase;    Sarcoplasmic reticulum;    Skeletal muscle;    S-nitrosylation;    dcGMP;    N 2;    O 3′-dibutyrylguanosine 3′;    5′-cyclic monophosphoric acid;    DTT;    dithiothreitol;    GAPDH;    glyceraldehyde-3-phosphate dehydrogenase;    GSNO;    S-nitrosoglutathione;    Mops;    4-morpholinopropanesulfonic acid;    NO;    nitric oxide (including NO+;    NO;    NO−);    SNAP;    S-nitroso N-acetylpenicillamine;   

DOI  :  10.1016/0014-5793(96)00829-0

学科分类：生物化学/生物物理

来源: John Wiley & Sons Ltd.

【 摘 要 】

The sarcoplasmic reticulum-bound creatine kinase from rabbit skeletal muscle was inhibited by the nitric oxide donor S-nitrosoglutathione (GSNO). This led to a decrease in Ca²⁺ uptake in sarcoplasmic reticulum vesicles when the transport was driven by ATP generated from phosphocreatine and ADP. In contrast, the Ca²⁺ transport measured using 2 mM ATP as substrate was unaffected by GSNO up to 200 μM. GSNO (5–20 μM) inhibited the activity of both soluble and membrane-bound creatine kinase. Oxyhemoglobin (15–40 μM) protected creatine kinase against inactivation by GSNO. The inhibition by 10 μM GSNO was reversed by the addition of dithiothreitol (2 mM). The results indicate that nitric oxide (NO, including NO⁺, NO and NO⁻) inactivates creatine kinase in vitro by promoting nitrosylation of critical sulphydryl groups of the enzyme.

【 授权许可】

Unknown