Garlid K D, Jabůrek M, Jezek P
Department of Biochemistry and Molecular Biology, Oregon Graduate Institute of Science and Technology, Portland 97291-1000, USA.
FEBS Lett. 1998 Oct 30;438(1-2):10-4. doi: 10.1016/s0014-5793(98)01246-0.
The effort to understand the mechanism of uncoupling by UCP has devolved into two models - the fatty acid protonophore model and the proton buffering model. Evidence for each hypothesis is summarized and evaluated. We also evaluate the obligatory requirement for fatty acids in UCP1-mediated uncoupling and the question of fatty acid affinity for UCP1. The structural bases of UCP transport function and nucleotide inhibition are discussed in light of recent mutagenesis studies and in relationship to the sequences of newly discovered UCPs.
对解偶联蛋白(UCP)解偶联机制的研究已发展为两种模型——脂肪酸质子载体模型和质子缓冲模型。对每种假说的证据进行了总结和评估。我们还评估了UCP1介导的解偶联中脂肪酸的必需要求以及脂肪酸对UCP1的亲和力问题。根据最近的诱变研究并结合新发现的UCP序列,讨论了UCP转运功能和核苷酸抑制的结构基础。