Schroeder F, Butko P, Nemecz G, Scallen T J
Department of Pharmacology, College of Pharmacy, University of Cincinnati, Ohio 45267-0004.
J Biol Chem. 1990 Jan 5;265(1):151-7.
The fluorescent sterol delta 5,7,9(11)-dehydroergostatetraen-3 beta-ol (dehydroergosterol) was used as an analogue of cholesterol to examine the molecular interaction of purified rat liver sterol carrier protein-2 (SCP-2) with sterol. The binding of dehydroergosterol to SCP-2 was evidenced by light scatter and by fluorescence polarization, lifetime, limiting anisotropy, and rotational relaxation time of dehydroergosterol. In addition, energy transfer efficiency from SCP-2 tryptophan to dehydroergosterol was 96%, indicating that the apparent distance, R, between the SCP-2 tryptophan (energy donor) and the dehydroergosterol (energy acceptor) was 13.7 A. Scatchard binding analysis of light scatter, lifetime, and energy transfer data all indicated a 1:1 molar stoichiometry with Kd = 1.2, 1.6, and 1.3 microM, respectively. SCP-2 enhanced the activity of microsomal acyl-CoA:cholesterol acyltransferase through transfer of [3H]cholesterol from donor palmitoyloleoyl phosphatidylcholine/cholesterol small unilamellar vesicles to rat liver microsomes containing the enzyme. A recently developed fluorescence assay utilizing dehydroergosterol fluorescence polarization (Nemecz, G., Fontaine, R. N., and Schroeder, F. (1988) Biochim. Biophys. Acta 948, 511-521; Nemecz, G., and Schroeder, F. (1988) Biochemistry 27, 7740-7749) was applied to examine the effect of SCP-2 on sterol exchange. In the absence of SCP-2, two spontaneously exchangeable sterol domains were observed in palmitoyloleoyl phosphatidylcholine/sterol (65:35 molar ratio) small unilamellar vesicles. SCP-2 enhanced the rate of exchange of the faster exchanging domain 2-fold. The transfer rate of the more slowly exchangeable sterol domain and the fraction of cholesterol represented by each domain were not affected. These results demonstrate the utility of dehydroergosterol to probe SCP-2 interactions with sterols and are indicative of a physiological role for SCP-2 as a soluble sterol carrier.
荧光甾醇δ5,7,9(11)-脱氢麦角四烯-3β-醇(脱氢麦角固醇)被用作胆固醇的类似物,以研究纯化的大鼠肝脏甾醇载体蛋白-2(SCP-2)与甾醇的分子相互作用。通过光散射以及脱氢麦角固醇的荧光偏振、寿命、极限各向异性和旋转弛豫时间,证实了脱氢麦角固醇与SCP-2的结合。此外,从SCP-2色氨酸到脱氢麦角固醇的能量转移效率为96%,这表明SCP-2色氨酸(能量供体)与脱氢麦角固醇(能量受体)之间的表观距离R为13.7埃。对光散射、寿命和能量转移数据进行的Scatchard结合分析均表明摩尔化学计量比为1:1,解离常数Kd分别为1.2、1.6和1.3微摩尔。SCP-2通过将[3H]胆固醇从供体棕榈酰油酰磷脂酰胆碱/胆固醇小单层囊泡转移到含有该酶的大鼠肝脏微粒体中,增强了微粒体酰基辅酶A:胆固醇酰基转移酶的活性。利用脱氢麦角固醇荧光偏振的一种最新开发的荧光测定法(Nemecz, G., Fontaine, R. N., and Schroeder, F. (1988) Biochim. Biophys. Acta 948, 511 - 521; Nemecz, G., and Schroeder, F. (1988) Biochemistry 27, 7740 - 7749)被用于研究SCP-2对甾醇交换的影响。在没有SCP-2的情况下,在棕榈酰油酰磷脂酰胆碱/甾醇(摩尔比65:35)小单层囊泡中观察到两个可自发交换的甾醇结构域。SCP-2使交换较快的结构域的交换速率提高了2倍。交换较慢的甾醇结构域的转移速率以及每个结构域所代表的胆固醇比例均未受到影响。这些结果证明了脱氢麦角固醇在探测SCP-与甾醇相互作用方面的效用,并表明SCP-2作为一种可溶性甾醇载体具有生理作用。