Alfred Wegener Institute for Polar and Marine Research, 27515 Bremerhaven, Germany.
Anal Biochem. 2011 Jun 15;413(2):203-5. doi: 10.1016/j.ab.2011.02.023. Epub 2011 Feb 20.
NanoDrop spectrophotometry and NanoDrop fluorospectrometry are used almost exclusively to determine the concentrations of nucleic acids and proteins. We propose that NanoDrop fluorospectrometry can also be applied for measuring enzyme activities using fluorogenic substrates such as the proteolytic activities of the 26S proteasome. Because the NanoDrop ND-3300 device requires only 2 μl of sample, the amount of sample extract, substrate, and cofactors used for an enzyme assay can be significantly reduced. In this report, we present exemplary microassays for proteasomal activities (chymotrypsin-, trypsin-, and PGPH [peptidyl-glutamyl peptide hydrolase]-like sites) in extracts of isolated hemocytes from a marine crab, Cancer pagurus (Crustaceae).
NanoDrop 分光光度法和 NanoDrop 荧光分光光度法几乎专门用于测定核酸和蛋白质的浓度。我们提出,NanoDrop 荧光分光光度法也可以用于测量荧光底物(如 26S 蛋白酶体的蛋白水解活性)的酶活性。由于 NanoDrop ND-3300 设备仅需要 2 μl 的样品,因此用于酶测定的样品提取液、底物和辅因子的量可以显著减少。在本报告中,我们展示了来自海洋蟹 Cancer pagurus(Crustaceae)分离的血淋巴细胞提取物中蛋白酶体活性(糜蛋白酶、胰蛋白酶和 PGPH [肽基-谷氨酰肽水解酶]样位点)的微分析示例。