Skripal I G, Weeks J R, Greenleaf A L
Acta Biochim Biophys Hung. 1986;21(3):215-24.
The binding of wheat germ RNA polymerase II to five different dye-ligand chromatography gels (Matrex gels, Amicon Corp.) was tested. A quantitative binding of the enzyme to four of the gels, namely Dyematrex gels Blue A, Blue B, Red A and Green A was observed. Only the Orange A gel column failed to bind the enzyme strongly. Nearly 100% of the activity could be recovered from the Green A column by elution with high salt concentration and high pH. Under these conditions only a part of the activity was eluted from the other three columns since the enzyme bound tightly. Enzyme activity could be removed from the columns by elution with nucleotide substrates, but the yield from the Blue A, Blue B and Red A columns was still low (7 to 42%). The Green A Matrex gel appeared to be useful for the purification and analysis of RNA polymerase.
对小麦胚RNA聚合酶II与五种不同的染料配体层析凝胶(Matrex凝胶,密理博公司)的结合情况进行了测试。观察到该酶与四种凝胶,即Dyematrex凝胶蓝A、蓝B、红A和绿A发生了定量结合。只有橙A凝胶柱未能强烈结合该酶。通过高盐浓度和高pH洗脱,几乎100%的活性可从绿A柱上回收。在这些条件下,由于酶紧密结合,只有一部分活性从其他三根柱上洗脱下来。通过核苷酸底物洗脱可将酶活性从柱上除去,但蓝A、蓝B和红A柱的回收率仍然很低(7%至42%)。绿A Matrex凝胶似乎可用于RNA聚合酶的纯化和分析。