Molecular Biophysics, University of Kaiserslautern, Erwin-Schrödinger-Str. 13, 67663 Kaiserslautern (Germany).
Angew Chem Int Ed Engl. 2015 Apr 20;54(17):5069-73. doi: 10.1002/anie.201412359. Epub 2015 Mar 9.
Surfactants carrying fluorocarbon chains hold great promise as gentle alternatives to conventional hydrocarbon-based detergents for the solubilization and handling of integral membrane proteins. However, their inertness towards lipid bilayer membranes has limited the usefulness of fluorinated surfactants in situations where detergent-like activity is required. We demonstrate that fluorination does not necessarily preclude detergency, as exemplified by a fluorinated octyl maltoside derivative termed F6 OM. This nonionic compound readily interacts with and completely solubilizes phospholipid vesicles in a manner reminiscent of conventional detergents without, however, compromising membrane order at subsolubilizing concentrations. Owing to this mild and unusual mode of detergency, F6 OM outperforms a lipophobic fluorinated surfactant in chaperoning the functional refolding of an integral membrane enzyme by promoting bilayer insertion in the absence of micelles.
氟碳链表面活性剂作为传统碳氢化合物基清洁剂的温和替代品,在溶解和处理完整膜蛋白方面具有很大的应用前景。然而,它们对脂质双层膜的惰性限制了氟化表面活性剂在需要清洁剂样活性的情况下的用途。我们证明,氟化不一定会排除去污性,例如,一种被称为 F6 OM 的氟化辛基麦芽糖苷衍生物就是例证。这种非离子化合物与磷脂囊泡容易相互作用,并以类似于传统清洁剂的方式完全溶解它们,而在亚溶解浓度下不会破坏膜的有序性。由于这种温和且不寻常的去污方式,F6 OM 在促进双层插入而无需形成胶束的情况下,在不使用疏脂性氟化表面活性剂的情况下,能够更好地护送一种完整膜酶的功能重折叠。