Kochert Brent A, Iacob Roxana E, Wales Thomas E, Makriyannis Alexandros, Engen John R
Department of Chemistry and Chemical Biology, Northeastern University, Boston, MA, USA.
Center for Drug Discovery, Northeastern University, Boston, MA, USA.
Methods Mol Biol. 2018;1764:153-171. doi: 10.1007/978-1-4939-7759-8_10.
Hydrogen-deuterium exchange (HDX) mass spectrometry (MS) can provide valuable information about binding, allostery, and other conformational effects of interaction in protein complexes. For protein-ligand complexes, where the ligand may be a small molecule, peptide, nucleotide, or another protein(s), a typical experiment measures HDX in the protein alone and then compares that with HDX for the protein when part of the complex. Multiple factors are critical in the design and implementation of such experiments, including thoughtful consideration of the percent protein bound, the effects of the labeling protocol on the protein complex, and the dynamic range of the analysis method. With careful planning and techniques, HDX MS analysis of protein complexes can be very informative.
氢-氘交换(HDX)质谱(MS)能够提供有关蛋白质复合物中相互作用的结合、变构及其他构象效应的有价值信息。对于蛋白质-配体复合物而言,其中的配体可能是小分子、肽、核苷酸或其他蛋白质,典型的实验是先测量蛋白质自身的HDX,然后将其与蛋白质作为复合物一部分时的HDX进行比较。在设计和实施此类实验时,多个因素至关重要,包括对蛋白质结合百分比的审慎考量、标记方案对蛋白质复合物的影响以及分析方法的动态范围。通过精心规划和运用相关技术,蛋白质复合物的HDX MS分析能够提供非常丰富的信息。