The properties of the outer hairy layer of casein micelles have been studied using several methods. Viscosity and light-scattering measurements have been performed on rennet-destabilized skim milk at different concentrations of calcium. We have reproduced the known result that calcium promotes destabilization at relatively high κ-casein surface coverages (even at only 50% of the κ-casein molecules cut off). This suggests that calcium bridges contribute to the casein micelle attraction. The effect may be direct by calcium-mediated bridging of β-casein or αs1-casein (phosphate/carboxylate) or κ-casein (carboxylate) or indirect by altering the interplay between several types of caseins in the micelle. In the analysis of the experiments, we make use of an adhesive hard sphere approximation. The casein hairy layer has further been modeled by a self-consistent field (SCF) theory in which coarse-grained molecular details were included. In these calculations the effect of calcium bridges cannot directly be accounted for. It is shown that a κ-casein layer induces repulsive interactions of mainly steric origin. Cutting the N-terminus part results in reduced (shorter-ranged) repulsive pair potentials, which still dominate over the van der Waals attraction. As a result of the altered interplay between the several types of casein molecules during the renneting process, the αs1-casein concentration in the outer hairy layer may increase. Again using the SCF model, but now using a less-detailed description of the system, we examine a possible result of this. We confirm that diblock copolymers (simple model for κ-casein) and diblock copolymer with shorter soluble block (simple model for para-κ-casein) give repulsion and triblock copolymers (simple model for αs1-casein) give attraction by means of bridging (adsorption). The renneting process is simulated by increasing the ratio of model para-κ-casein to κ-casein at a fixed αs1-casein concentration. As a result, the potential shifts from repulsive to attractive. We show that by reducing the range of repulsive interactions of the diblock copolymers, we can make room available to express the attractive contributions of the model αs1-casein. This comprises a novel molecular-based mechanism for the renneting process.