Download PDF by Alexander A. Mironov, Margit Pavelka: The Golgi Apparatus: State of the art 110 years after

By Alexander A. Mironov, Margit Pavelka

ISBN-10: 3211763090

ISBN-13: 9783211763094

ISBN-10: 3211763104

ISBN-13: 9783211763100

For over one hundred ten years The Golgi complicated has been on the heart of curiosity and medical debates. It constitutes a primary crossroads in secretory and endocytic site visitors. despite the fact that, regardless of hundreds of thousands of information identified approximately structure, association, and shipping mechanisms around the Golgi stacks of cisternae, and in all likelihood because of this plethora of knowledge, it's tough to discover motives, how the advanced process works.

This booklet summarizes all new facts got after improvement of equipment of Golgi advanced sub fractionation, molecular biology and microscopy gathering the complete diversity of craftsmanship, assorted issues of view and varied techniques. The booklet is dedicated to molecular modes of the functionality of the Golgi gear as an entire, taking into consideration all experimental information whether they contradict latest types of Golgi functionality. the purpose of the ebook is to make the sensible association of the Golgi equipment extra comprehensible via holding it so simple as attainable but in addition as complete as possible.

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Additional resources for The Golgi Apparatus: State of the art 110 years after Camillo Golgi’s discovery

Example text

One of the less known version of the vesicular model implied that tubules serve as retro- Golgi apparatus as a crossroads * 31 Figure 4. Scheme showing the main principles of intracellular transport. A The dissociation (mainly vesicular) model of intracellular transport. Initially, membrane buds are formed on the first (proximal) compartment with the help of protein coat and then, after fission and subsequent uncoating, coat-dependent vesicles move to the second (distal) compartment and are captured by tethering system.

This lack of specificity is particularly apparent in in vitro mixing experiments using bacterially expressed mammalian as well as yeast SNARE proteins (Yang et al. 1999; Fasshauser et al. 1999; Tsui and Banfield 2000). Recent evidence suggests that non-cognate SNARE complexes form in cells, but that cells have some, as yet to be identified mechanism, which selects only the physiologically relevant complexes for use in membrane fusion reactions (Bethani et al. 2007). Thus, the identification of SNARE–SNARE interactions by co-immune precipitation may not be sufficient to assign particular SNAREs to a functional complex (Bethani et al.

J Electron Microsc 33: 19–33 Seemann J, Jokitalo E, Pypaert M, Warren G (2000) Matrix proteins can generate the higher order architecture of the Golgi apparatus. Nature 407: 1022–1026 Sesso A, De Faria FP, Iwamura ESM, Correa H (1994) A three-dimensional reconstruction study of the rough ER–Golgi interface in serial thin sections of the pancreatic acinar cell of the rat. J Cell Sci 107: 517–528 Shewan AM, Van Dam EM, Martin S, Luen TB, Hong W, Bryant NJ, James DE (2003) GLUT4 recycles via a trans-Golgi network (TGN) subdomain enriched in Syntaxins 6 and 16 but not TGN38: involvement of an acidic targeting motif.

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The Golgi Apparatus: State of the art 110 years after Camillo Golgi’s discovery by Alexander A. Mironov, Margit Pavelka

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