Understanding of the mechanistic progess of amyloid-beta peptide (A beta) aggregation is critical for elucidating the underlying pathogenesis of Alzheimers disease (AD). Herein, we report for the first time the effects of two cholesterol derivatives, negatively charged cholesterol sulfate (cholesterol-SO4) and positively charged 3 beta-[N-(dimethylaminoethane)carbamoyl]-cholesterol (DC-cholesterol), on the fibrillization of A beta 40. Our results demonstrate that both of the nonvesicular forms of cholesterol-SO4 and DC-cholesterol moderately accelerate the aggregation rate of A beta 40. This effect is similar to that observed for unmodified cholesterol, indicating the importance of hydrophobic interactions in binding of A beta 40 to these steroid molecules. Furthermore, we show that the vesicles formed at higher concentrations of anionic cholesterol-SO4 facilitate A beta 40 aggregation rate markedly. In contrast, the cationic DC-cholesterol vesicles show the ability to inhibit A beta 40 fibril formation under appropriate experimental conditions. The results suggest that the electrostatic interactions between A beta 40 and the charged vesicles can be of great importance in regulating A beta 40-vesicle interaction. Our results also indicate that the structural properties of the aggregates of the cholesterol derivatives, including the surface charge and the size of the vesicles, are critical in regulating the effects of these vesicles on A beta 40 aggregation kinetics.