Photoinitiated surface-selective graft copolymn. onto polypropylene (PP) microfiltration membranes was performed using two different methods for coating the photoinitiator, benzophenone (BP), on the membrane surface. An already established adsorption method and a novel method based on preswelling of the PP in heptane, subsequent solvent exchange, and thus entrapping of the BP in the surface layer of the PP had been evaluated. With acrylic acid (AA) as the monomer, functional polymer brush structures on the entire membrane pore surface were obtained. Further variations of the grafted layer had been achieved by copolymn. of AA with acrylamide (AAm) and methylene bisacrylamide (MBAA). Characterization had been done mainly by detailed measurements of membrane permeability including pH dependency as well as the reversible binding of a protein (lysozyme, Lys) under membrane chromatog. conditions. Compared with BP adsorption, the BP entrapping method yielded a less dense grafted layer with longer PAA chains at the same degree of functionalization (DG). This was due to somewhat lower immobilized BP amts., but also less side reactions via nonselective photoinitiated crosslinking by dissolved BP. Unexpected properties of the PAA-co-AAm brush layers were their even larger swelling/deswelling as a function of a pH change (above and below the pKa of PAA) as compared with the PAA brushes. Both PAA-co-AAm and cross-linked PAA-co-MBAA layers showed Lys binding capacities-more than 10 times higher than monolayer adsorption onto the unmodified PP membrane surface-and quant. recoveries similar to PAA of the same DG; and the highest efficiencies of protein binding (Lys amt. relative to amt. graft copolymer) were achieved with the membranes prepd. by the entrapping method. In general, the more controlled BP entrapping method had distinct advantages in terms of the control of grafted layer structure leading to an improved membrane adsorber performance.