Aberrant guanosine triphosphate-beta-tubulin interaction in Alzheimer's disease.

Author: Khatoon S, Campbell SR, Haley BE, Slevin JT.

Source: Ann Neurol.

Year: 1989

Comment:

The researchers note, "In summary, in AD [Alzheimer's disease] brain tissue the GTP binding site involved in promoting tubulin polymerization is dramatically reduced with regard to its ability to interact with added guanine nucleoside triphosphates. Furthermore, this biochemical aberration correlates with a recognized pathological hallmark of AD, the neurofibrillary tangle."

Abstract / Excerpt:

“Guanosine triphosphate (GTP) is an absolute requirement for tubulin polymerization in situ. The nucleotide photoaffinity probe 8-azidoguanosine 5′-triphosphate (8N3GTP) has been shown to be a biological mimic of GTP in this system and, also, an effective active site probe of the exchangeable GTP binding site. Using [32P]8N3GTP we demonstrate that the exchangeable GTP site of the beta subunit of tubulin is available to added guanine nucleotide in normal aged brain homogenates, whereas it is variably unavailable in Alzheimer’s diseased brain. Inability of 8N3GTP to photolabel beta tubulin appears to be associated with neurofibrillary tangle density. These results support the hypothesis that microtubule formation is abnormal in brains affected by Alzheimer’s disease.”

Citation:

Khatoon S, Campbell SR, Haley BE, Slevin JT. Aberrant guanosine triphosphate-beta-tubulin interaction in Alzheimer's disease. Ann Neurol. 1989; 26(2):210-5.