BACKGROUND

Prostheses aim to enhance the quality of life, independence, mobility, and safety of amputees. The frequency of amputations worldwide has created an increased demand for improved prosthetic technologies. Within developing countries, the population with physical disabilities in need of a prosthesis is estimated at about 0.5%. There are currently almost 2 million people living with limb loss in the United States. In 2050, this amount will exceed 3 million people^[1].

Over the past decade, many types of prostheses have been created. One of them is the myoelectric prosthesis, which captures the electromyographic (EMG) signal of residual limb muscle through surface electrodes on the skin. These kinds of robotic prostheses allow amputees to recover some autonomy and to accomplish simple everyday gestures. However, they are still limited by a number of controllable movements and by the lack of sensory feedback ^[1].

Today, the direct attachment of the prosthesis to the skeleton introduces the concept of osseointegration. This kind of prosthesis provides the patient with precise and reliable control of the new limb, regardless of the environmental conditions or the position. The opportunity to record and stimulate the neuromuscular system allows intuitive control and a better understanding of sensory perception ^[2].

The central nervous system (CNS), composed of the brain and the spinal cord, helps integrating, influencing and coordinating activities across the whole organism. The neural tissues bring information from one region of the body to another by sending electrical signals along the axon ^[3]. The efferent motor neurons of the peripheral nervous system (PNS) communicate with muscles and are under voluntary control. They go from the spinal cord to the arms, hands, legs, and feet and allow for nerve impulses to be transmitted from the CNS, leading to an action ^[3]. To increase the electrical signal speed, axons are surrounded by myelin, produced by another type of cells called Schwann cells. These cells twist around the axon and prevent the loss of the electrical signal^[4]. After limb amputation, the main issue within the human-machine communication is due to the damage inflicted on the nerves. In fact, the electrical signal cannot be transmitted because peripheral nerve cells are no longer able to activate target muscles or relay sensory information from the limbs back to the brain.

OUR SOLUTION

The central idea of our project is to find a way to help the motor nerves of amputees grow back and connect to our interface. Literature studies led us to think of neurotrophins as the perfect molecules to start our research on. This family of peptides are growth factors specialized in the regulation of neuronal development, survival, plasticity and nervous system function^[5].

What are neurotrophins?

The first neurotrophin to be discovered was the Nerve Growth Factor (NGF). It was described in 1952 by Rita Levy Montalcini and Viktor Hamburger ^[6]. Since then, many other neurotrophins have been discovered (BDNF, NT-3, NT-4, NT-6) ^[7] and much progress has been achieved towards understanding how they work. Yet, NGF is still considered a “prototype neurotrophin” ^[5] and is generally used as an example to describe the function of these peptides. For this reason, we chose to clone this polypeptide into our bacteria, creating the first component of the NeuronArch project.

The ambiguity between NGF and proNGF.

The mature-NGF protein results from the cleavage of β-NGF from a bigger protein called proNGF, which contains a pro-sequence and β-NGF (Figure 1). Both proNGF and β-NGF proteins are biologically active, and there is, to this date, some sort of uncertainty about the exact effect of proNGF.

Figure 1: Structure of the proNGF gene. Adapted from Ivanisevic, 2013.

Indeed, whereas there is no doubt that β-NGF is a neurotrophic factor, it has still not been determined exactly whether proNGF is a neurotrophic or an apoptotic factor ^[8]. Many articles are still in contradiction on this matter and part of the reason is linked with the biological pathways by which both proteins act on neurons. Two receptors are involved in their signaling: tropomyosin-related kinase A (TrkA) and the p75 neurotrophin receptor (p75^NTR). The two proteins (proNGF and β-NGF) are able to bind both receptors, but it is globally accepted that β-NGF has a higher affinity for TrkA and proNGF has a higher affinity for p75^NTR. Figure 2 shows a big picture of how the two signaling pathways are thought to work.

Figure 2: NGF versus proNGF signaling pathways. Adapted from Wang, 2014.

At this point, it might seem that choosing to clone β-NGF in the bacteria of our interface would be a better idea than proNGF. However, a few other information led us to think the other way around. First, despite the existing controversy, proNGF has been proven to exhibit a neurotrophic activity on some neural cells, even though it is not as strong as mature β-NGF (there is a fivefold activity difference) ^[10]. This neurotrophic activity is likely generated by a p75^NTR-dependent mechanism and depends on the proportion of TrkA and p75^NTR in the neural cells ^[11]. Moreover, TrkA is mainly expressed in three types of neurons: peripheral sensory neurons, sympathetic neurons and basal forebrain cholinergic neurons, whereas p75^NTR is more evenly dispersed in different types of neurons ^[9]. Thus, expressing proNGF in our case seems like a good choice. Furthermore, several articles support the idea that the pro-sequence of NGF facilitates, and is even absolutely necessary, for the proper folding of the protein when it is recombinantly expressed in bacteria. This is particularly relevant as this protein contains three disulfide bonds and is particularly difficult to express using synthetic biology while keeping its function ^{[12] [13]}.

Considering all this information, we finally chose to clone proNGF in our interface.

How to produce and secrete proNGF in Escherichia coli ?

Figure 3: proNGF production and secretion from E. coli

The composition of our final composite biobrick BBa_K2616000 is detailed in the PARTS submenu of this wiki.

Concretely, it expresses two main proteins:

proNGF, linked to HlyA, a type I secretion system export signal in E. coli. Between the two, we added a TEV protease cleavage site.
TEV protease, a protein from Tobacco Etch Virus that recognizes a specific sequence and cleaves it. We also linked the TEV protease to the same export signal.

Once exported from the cell, the TEV protease can cleave the proNGF from HlyA and free the pro-neurotrophin in the external medium.

RESULTS

Achievements:

Successfully cloned a biobrick coding for secretion of NGF in pET43.1a and iGEM plasmid backbone pSB1C3, creating a new part BBa_K2616000.
Successfully sequenced BBa_K2616000 in pSB1C3 and sent to iGEM registry.
Successfully co-transformed E. coli with plasmid secreting proNGF and plasmid expressing the secretion system, creating bacteria capable of secreting NGF in the medium.
Successfully characterized production of proNGF thanks to mass spectrometry and western blot.
Successfully observed axon growth in microfluidic chip in presence of commercial NGF.
Successfully observed axon growth in 96-well plate in presence of our recombinant proNGF.

Next steps:

Purify secreted proNGF, and characterize its effects on neuron growth thanks to our microfluidic device.
Global proof of concept in a microfluidic device containing neurons in one of the chamber, and our engineered bacteria in the other.

Visit the RESULTS page to get more information

REFERENCES

P. F. Pasquina, B. N. Perry, M. E. Miller, G. S. F. Ling, and J. W. Tsao, “Recent advances in bioelectric prostheses,” Neurol. Clin. Pract., vol. 5, no. 2, pp. 164–170, Apr. 2015.
Y. Li and R. Brånemark, “Osseointegrated prostheses for rehabilitation following amputation,” Unfallchirurg, vol. 120, no. 4, pp. 285–292, Apr. 2017.
A. Farley, C. Johnstone, C. Hendry, and E. McLafferty, “Nervous system: part 1,” Nurs. Stand., vol. 28, no. 31, pp. 46–51, Apr. 2014.
“Schwann Cells,” PubMed Health. [Online]. Available: https://www.ncbi.nlm.nih.gov/pubmedhealth/PMHT0025728/. [Accessed: 27-Sep-2018].
L. Ivanisevic and H. U. Saragovi, “Neurotrophins,” in Handbook of Biologically Active Peptides, Elsevier, 2013, pp. 1639–1646.
S. Cohen, R. Levi-Montalcini, and V. Hamburger, “A nerve growth-stimulating factor isolated from sarcom AS 37 and 180,” Proc. Natl. Acad. Sci. U. S. A., vol. 40, no. 10, pp. 1014–8, Oct. 1954.
S. Razavi, G. Nazem, M. Mardani, E. Esfandiari, S. Esfahani, and H. Salehi, “Neurotrophic factors and their effects in the treatment of multiple sclerosis,” Adv. Biomed. Res., vol. 4, no. 1, p. 53, 2015.v
M. Fahnestock, G. Yu, and M. D. Coughlin, “ProNGF: a neurotrophic or an apoptotic molecule?,” 2004, pp. 101–110.
H. Wang et al., “The Nerve Growth Factor Signaling and Its Potential as Therapeutic Target for Glaucoma,” Biomed Res. Int., vol. 2014, pp. 1–10, 2014.
M. Fahnestock et al., “The nerve growth factor precursor proNGF exhibits neurotrophic activity but is less active than mature nerve growth factor,” J. Neurochem., vol. 89, no. 3, pp. 581–592, 2004.
L. Howard, S. Wyatt, G. Nagappan, and A. M. Davies, “ProNGF promotes neurite growth from a subset of NGF-dependent neurons by a p75^NTR-dependent mechanism,” Development, vol. 140, no. 10, pp. 2108–2117, 2013.
A. Rattenholl, H. Lilie, A. Grossmann, A. Stern, E. Schwarz, and R. Rudolph, “The pro-sequence facilitates folding of human nerve growth factor from Escherichia coli inclusion bodies,” Eur. J. Biochem., vol. 268, no. 11, pp. 3296–3303, 2001.
M. Kliemannel et al., “The mature part of proNGF induces the structure of its pro-peptide,” FEBS Lett., vol. 566, no. 1–3, pp. 207–212, May 2004.