Manchester Institute of Biotechnology, University of Manchester, Princess Street, Manchester, M1 7DN, UK.
Department of Chemistry, King's College London, 7 Trinity Street, London, SE1 1DB, UK.
Angew Chem Int Ed Engl. 2022 Jun 20;61(25):e202115047. doi: 10.1002/anie.202115047. Epub 2022 Apr 21.
The effect of temperature on the stability of proteins is well explored above 298 K, but harder to track experimentally below 273 K. Variable-temperature ion mobility mass spectrometry (VT IM-MS) allows us to measure the structure of molecules at sub-ambient temperatures. Here we monitor conformational changes that occur to two isotypes of monoclonal antibodies (mAbs) on cooling by measuring their collision cross sections (CCS) at discrete drift gas temperatures from 295 to 160 K. The CCS at 250 K is larger than predicted from collisional theory and experimental data at 295 K. This restructure is attributed to change in the strength of stabilizing intermolecular interactions. Below 250 K the CCS of the mAbs increases in line with prediction implying no rearrangement. Comparing data from isotypes suggest disulfide bridging influences thermal structural rearrangement. These findings indicate that in vacuo deep-freezing minimizes denaturation and maintains the native fold and VT IM-MS measurements at sub ambient temperatures provide new insights to the phenomenon of cold denaturation.
在 298 K 以上,温度对蛋白质稳定性的影响已经得到了充分的研究,但在 273 K 以下,这种影响更难通过实验来跟踪。变温离子淌度质谱(VT IM-MS)使我们能够在亚环境温度下测量分子的结构。在这里,我们通过测量两种单克隆抗体(mAb)亚型在冷却过程中发生的构象变化来监测它们的碰撞截面(CCS),在离散的漂移气体温度下从 295 到 160 K 进行测量。在 250 K 时的 CCS 大于根据 295 K 时的碰撞理论和实验数据预测的值。这种重构归因于稳定分子间相互作用强度的变化。在 250 K 以下,mAb 的 CCS 与预测值一致增加,这意味着没有重新排列。比较同型物的数据表明,二硫键桥接影响热结构重排。这些发现表明,在真空中深冻可最大限度地减少变性并保持天然折叠,而在亚环境温度下进行的 VT IM-MS 测量为冷变性现象提供了新的见解。