Protocol for reconstituting enzymatic activities for ultra-large histone methyltransferases NSD1 and SETD2 using a baculovirus expression system.

Expression and reconstitution of large proteins in the human proteome are challenging and often require the use of a mammalian cell expression system that is costly and inefficient. Here, we present a protocol to reconstitute catalytically active, full-length NSD1 (nuclear receptor binding SET domain protein 1) and SETD2 (SET domain containing 2, histone lysine methyltransferase) using a clonal baculovirus expression system. We describe steps for producing baculovirus, clonal selection, and protein reconstitution. We then detail procedures for using animatic assays. For complete details on the use and execution of this protocol, please refer to Hsu et al.(1).