The association behavior of apoferritin species with the anionic porphyrins, 5,10,15,20-tetrakis(4-sulfonatophenyl)porphyrin (H2TPPS4-) and its zinc(II) complex (ZnTPPS4-), which are water-soluble even in acidic solutions, was investigated for the first time through UV-Vis absorption and fluorescence spectroscopy in order to evaluate a potential ability of apoferritin as a stimuli-responsive molecular capsule. The absorption maximum wavelengths of both porphyrins were redshifted and the fluorescence intensity decreased, indicating the effective association between apoferritin species and the porphyrins, although it depended on the pH adjustment procedure. At pH 2, the ZnTPPS4- associated with apoferritin subunits without demetallating and protonating, while the free base porphyrin formed the J-aggregate of the diprotonated species (H4TPPS2-)(n), with extremely low fluorescence. As the concentration of apoferritin subunits increased, the H2TPPS4--subunits associates were formed accompanied by recovering the fluorescence. The association stoichiometries of 1 or 2 subunits/porphyrin obtained under neutral and acidic conditions. The significantly large association constant of ZnTPPS4- as compared with that of H2TPPS4- indicated that the coordination to the zinc(II) center strongly contributes to the association in addition to the electrostatic interaction between apoferritin subunits and the porphyrin under acidic conditions.