Yadav Rajeev, Sengupta Bhaswati, Das Shyamashis, Sen Pratik
Department of Chemistry, Indian Institute of Technology Kanpur, Kanpur, UP 208 016, India.
Department of Chemistry, University of Michigan, Ann Arbor, MI, United States.
Protein Pept Lett. 2018;25(4):339-349. doi: 10.2174/0929866525666180212111823.
Interaction of surfactants with proteins can decipher important information regarding the stability and behavior of proteins. For multi-domain proteins, these interactions vary domain wise and these details are crucial in understanding the contribution of different domains of the protein in its overall activity.
The objective of the present work is to study the interaction of surfactants with domain III of Human Serum Albumin (HSA) and to compare the same with the global interaction.
Interaction of the anionic Sodium Dodecyl Sulphate (SDS) and the Cationic Cetyltrimethylammonium Bromide (CTAB) surfactants with domain III of Human Serum Albumin (HSA) has been studied using 8-Anilino-1-Naphthalene-Sulphonate (ANS) as a fluorescent marker. Circular Dichroism (CD) spectroscopy has been used to study the protein-surfactant interaction for the overall protein.
SDS is found to interact sequentially with domain III of HSA having two detectable intermediate states in the binding process. In case of CTAB, we have observed only one intermediate state for its interaction with domain III. Although Quantum yield measurement can reflect the presence of such intermediate state, the overall conformational change of the HSA on addition of surfactants, studied by Circular Dichroism (CD) spectroscopy, and the ANS-Trp distance measurement by FRET could not resolve the presence of such intermediate states. The esterase activity of HSA in presence of different amount of surfactants is also in accordance with our above observation.
The interaction of both the surfactants with HSA is found to be sequential in nature. The most important conclusion revealed from our study is that the nature of protein-surfactant interaction is not same throughout the entire protein. Our study reveals that different parts of the multi-domain HSA have different affinity to the surfactant molecules.
表面活性剂与蛋白质的相互作用能够解读有关蛋白质稳定性和行为的重要信息。对于多结构域蛋白质而言,这些相互作用因结构域而异,而这些细节对于理解蛋白质不同结构域在其整体活性中的作用至关重要。
本研究的目的是研究表面活性剂与人血清白蛋白(HSA)结构域III的相互作用,并将其与整体相互作用进行比较。
使用8-苯胺基-1-萘磺酸盐(ANS)作为荧光标记,研究了阴离子十二烷基硫酸钠(SDS)和阳离子十六烷基三甲基溴化铵(CTAB)表面活性剂与人血清白蛋白(HSA)结构域III的相互作用。圆二色性(CD)光谱已用于研究整个蛋白质的蛋白质-表面活性剂相互作用。
发现SDS在结合过程中与HSA的结构域III依次相互作用,有两个可检测的中间状态。在CTAB的情况下,我们观察到其与结构域III相互作用只有一个中间状态。尽管量子产率测量可以反映这种中间状态的存在,但通过圆二色性(CD)光谱研究的表面活性剂添加后HSA的整体构象变化以及通过荧光共振能量转移(FRET)进行的ANS-色氨酸距离测量无法解析这种中间状态的存在。不同量表面活性剂存在下HSA的酯酶活性也与我们上述观察结果一致。
发现两种表面活性剂与HSA的相互作用本质上都是依次进行的。我们的研究揭示的最重要结论是,蛋白质-表面活性剂相互作用的性质在整个蛋白质中并不相同。我们的研究表明,多结构域HSA的不同部分对表面活性剂分子具有不同的亲和力。