Isolation of a matrix that binds medial Golgi enzymes

doi:10.1083/jcb.124.4.405

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Isolation of a matrix that binds medial Golgi enzymes

P Slusarewicz, T Nilsson, N Hui, R Watson and G Warren
Cell Biology Laboratory, Imperial Cancer Research Fund, London, United Kingdom.

Rat liver Golgi stacks were extracted with Triton X-100 at neutral pH. After centrifugation the low speed pellet contained two medial-Golgi enzymes, N-acetylglucosaminyltransferase I and mannosidase II, but no enzymes or markers from other parts of the Golgi apparatus. Both were present in the same structures which appeared, by electron microscopy, to be small remnants of cisternal membranes. The enzymes could be removed by treatment with low salt, leaving behind a salt pellet, which we term the matrix. Removal of salt caused specific re-binding of both enzymes to the matrix, with an apparent dissociation constant of 3 nM for mannosidase II. Re-binding was abolished by pretreatment of intact Golgi stacks with proteinase K, suggesting that the matrix was present between the cisternae.
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