Schliselfeld L H, Danon M J
Department of Pathology, New York Medical College, Valhalla, NY 10595, USA.
Clin Biochem. 1996 Feb;29(1):79-83. doi: 10.1016/0009-9120(95)02005-5.
Use fructose-2,6-diphosphate (fru-2,6-P2) for measuring phosphofructokinase (PFK) activity in muscles.
PFK activity was measured at 2 mmol/L MgCl2 and 5 mmol/L adenosine triphosphate (ATP) (mol/L MgCl2:mol/L ATP 0.4) without and with fru-2,6-P2.
Human muscle extracts had little PFK activity when assayed at mol/L MgCl2:mol/L ATP of 0.4 to 0.78 without fru-2,6-P2; 1.83 +/- 0.91 units/g muscle. Addition of fru-2,6-P2 produced an immediate 20- to 57-fold increase in activity; 52.8 +/- 12.5 units/g muscle. Raising the mol/L ratio of MgCl2 to ATP to 0.87 and higher without fru-2,6-P2 produced 34%-76% of the PFK activity seen with fru-2,6-P2. A PFK deficiency patient had a trace of activity, which was independent of mol/L MgCl2:mol/L ATP and not activated by fru-2,6-P2.
The almost complete absence of activity without fru-2,6-P2 at 0.40 mol/L MgCl2:mol/L ATP, and the restoration of maximum activity by fru-2,6-P2 provides an assay for verified PFK activity that could lead to a more accurate diagnosis in patients with PFK deficiency.
使用果糖 - 2,6 - 二磷酸(fru - 2,6 - P2)来测量肌肉中的磷酸果糖激酶(PFK)活性。
在存在和不存在fru - 2,6 - P2的情况下,于2 mmol/L氯化镁(MgCl2)和5 mmol/L三磷酸腺苷(ATP)(MgCl2摩尔浓度:ATP摩尔浓度为0.4)条件下测量PFK活性。
在MgCl2摩尔浓度:ATP摩尔浓度为0.4至0.78且不存在fru - 2,6 - P2的情况下检测时,人肌肉提取物的PFK活性很低;为1.83±0.91单位/克肌肉。添加fru - 2,6 - P2后活性立即增加20至57倍;达到52.8±12.5单位/克肌肉。在不存在fru - 2,6 - P2的情况下,将MgCl2与ATP的摩尔浓度比提高到0.87及更高时,产生的PFK活性为添加fru - 2,6 - P2时所见活性的34% - 76%。一名PFK缺乏症患者的活性痕迹与MgCl2摩尔浓度:ATP摩尔浓度无关,且不受fru - 2,6 - P2激活。
在0.40摩尔浓度的MgCl2:摩尔浓度的ATP条件下,不存在fru - 2,6 - P2时几乎完全没有活性,而fru - 2,6 - P2可恢复最大活性,这为验证PFK活性提供了一种检测方法,有助于对PFK缺乏症患者进行更准确的诊断。