Rampelt Heike, Mayer Matthias P, Bukau Bernd
Zentrum für Molekulare Biologie, der Universität Heidelberg, DKFZ-ZMBH Alliance, Heidelberg, Germany.
Methods Mol Biol. 2011;787:83-91. doi: 10.1007/978-1-61779-295-3_7.
The ATPase cycle of Hsp70 chaperones controls their transient association with substrate and, thus, governs their function in protein folding. Nucleotide exchange factors (NEFs) accelerate ADP release from Hsp70 which results in rebinding of ATP and release of the substrate. This chapter describes several methods suitable to study NEFs of Hsp70 chaperones. On the one hand, steady-state ATPase assays provide information on how the NEF influences progression of the Hsp70 through the entire ATPase cycle. On the other hand, nucleotide release can be measured directly using labeled nucleotides, which enables identification and further characterization of NEFs.
热休克蛋白70(Hsp70)伴侣蛋白的ATP酶循环控制着它们与底物的短暂结合,从而决定了它们在蛋白质折叠中的功能。核苷酸交换因子(NEFs)加速ADP从Hsp70的释放,这导致ATP的重新结合和底物的释放。本章介绍了几种适用于研究Hsp70伴侣蛋白的NEFs的方法。一方面,稳态ATP酶分析提供了关于NEF如何影响Hsp70在整个ATP酶循环中的进程的信息。另一方面,可以使用标记的核苷酸直接测量核苷酸的释放,这有助于鉴定NEFs并对其进行进一步表征。