As the recipients of the 2013 science Nobel prizes gather in Stockholm to celebrate and be celebrated, News & Views shares some expert opinions on the achievements honoured.
The recipients of the Nobel Prize in Physiology or Medicine are Randy W. Schekman, James E. Rothman and Thomas C. Südhof, for their discoveries on how cells deliver thousands of internally generated molecules to the right place at the right time (see figure).
Identification of the trafficking machinery
by Susan Ferro-Novick
In the late 1970s, Randy Schekman and Jim Rothman both strove to identify the cellular machinery that drives the secretory pathway, albeit by taking strikingly different approaches. Schekman and co-workers took advantage of yeast genetics to initially identify 23 genes, called SEC, whose products are required for protein secretion1,2. Rothman and colleagues used a biochemical approach to purify, by brute force, components of the mammalian secretory apparatus3.
As the SEC genes were characterized and several of their mammalian counterparts were identified, it became clear that Schekman and Rothman's independent approaches had converged and catalysed the field of membrane traffic. Schekman went on to focus on the 'coat' proteins that sort cellular cargo into a nascent vesicle. Rothman instead focused on the membrane-fusion machinery, which he called SNARE proteins4, and which is found in all eukaryotes (organisms that include fungi, plants and animals).
The ground-breaking work of these laureates has revolutionized our understanding of a basic cellular function — protein secretion. Whereas the genetic approach identified many of the components of the pathway, the biochemical assays facilitated elucidation of the components' functions. The laureates' seminal contributions paved the way for studies of many other cellular processes that rely on the secretory pathway, including cell polarization, cell migration and the degradative process of autophagy.
A turbocharger for membrane fusion
by Nils Brose
The realization that the membrane-fusion machinery is evolutionarily conserved from yeast cells to neurons posed a problem for neuroscientists. SNARE-mediated membrane fusion and protein secretion are rather slow, whereas the secretion of neurotransmitter molecules from synaptic vesicles in neurons occurs with millisecond precision and is tightly controlled by intracellular calcium ions, which can boost the vesicle fusion rate by up to 1 million times. Clearly, neuronal synapses could not rely only on SNAREs. They must contain a specialized protein machinery that boosts the somewhat sluggish SNARE machinery, thereby equipping synapses for their exquisite precision and speed.
When Rothman discovered the function of SNAREs in the early 1990s, Tom Südhof was well on his way to a systematic molecular cartography of synaptic communication between neurons and a functional analysis of synaptic-vesicle proteins — an endeavour that was co-pioneered with his long-term ally Reinhard Jahn. Südhof identified and characterized numerous key components of the synaptic-vesicle fusion apparatus and of the parallel regulatory machinery that makes synaptic secretion so fast5. Of greatest importance, he identified synaptotagmin, and showed that this protein is the enigmatic calcium sensor that 'turbocharges' synaptic-vesicle secretion6.
But the story of this year's Nobel laureates does not end here. From single-cell organisms to humans, each and every cellular process depends on the cellular logistics of membrane trafficking and the secretion of cellular cargo. Not surprisingly then, diseases as diverse as tetanus, botulism, haemophagocytic lymphohistiocytosis, epilepsy and even schizophrenia have been shown — or are at least thought — to be caused by defects in proteins that control cellular trafficking. And this is just the tip of the iceberg. Interfering with these processes for therapeutic purposes seems only steps away.
Novick, P., Field, C. & Schekman, R. Cell 21, 205–215 (1980).
Novick, P. & Schekman, R. Proc. Natl Acad. Sci. USA 76, 1858–1862 (1979).
Balch, W. E., Dunphy, W. G., Braell, W. A. & Rothman, J. E. Cell 39, 405–416 (1984).
Söllner, T. et al. Nature 362, 318–324 (1993).
McMahon, H. T., Missler, M., Li, C. & Südhof, T. C. Cell 83, 111–119 (1995).
Fernández-Chacón, R. et al. Nature 410, 41–49 (2001).
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