Pharmaceuticals from plants
Here's a very interesting article on how biotechnology is aiding in the development of pharmaceuticals.
Alisa
Pharmaceuticals from plants
By Sushmi Dey
Indian Express Newspapers (Mumbai) Limited via Express Pharma
August 25, 2006
Advances in biotechnology aided in the production of therapeutic proteins essential in a wide range of pharmaeuticals like monoclonal antibodies, enzymes and blood proteins.
Since the demand for these biopharmaceuticals is expected to increase, researchers all over the world are looking at ways to ensure that they will be available at significantly larger amounts and on a cost-effective basis. One such solution comes in the form of plant-made pharmaceuticals (PMPs), which are cheap to produce and store, easy to scale up for mass production and safer than those derived from animals.
The plus factor
The use of plants for medicinal purpose dates back to thousands of years, but genetic engineering of plants to produce desired biopharmaceuticals is a much more recent phenomenon. In normal circumstances, drugs are synthesised through strong chemical reactions or taken from natural sources such as texol or curcumin. The conventional system in place for the production of commercial protein has relied on microbial fermentation and mammalian cell lines. But according to studies, these systems have disadvantages in terms of cost, scalability, and safety that have promoted research into alternatives.
PMPs are a category of pharmaceutical proteins that are produced in 'live plants'. These live plants are genetically modified to produce drugs. "Plants can produce large amount of proteins in them," says Dr V Siva Reddy, Group Leader, Plant Transformation Group, ICGEB. Plants can express a protein in a very profitable manner by manipulation of genes or by the introduction of genes required to express a particular protein. Hence, pharmaceuticals can be produced in large quantity, and purity can be expressed in high levels.
Plants have emerged as one of the most promising general production platform for biologics. Plants allow cost-effective production of recombinant proteins on an agricultural scale, while eliminating risks of product contamination with endotoxins or human pathogens. In addition, with the use of plants in the production of recombinant protein, vaccine candidates can be expressed in edible plant organs, allowing them to be administered as unprocessed or partially processed material. However, in matters of efficacy, they are equivalent to the conventional drugs, informs Reddy.
Technology behind PMPs
In the process of producing PMPs, plants themselves act as factories to manufacture therapeutic proteins. Special proteins or compounds are expressed in different parts of plants, some specific tissues, such as whole leaves, whole seeds, or even specific regions of seeds or leaves. The whole process is meant to incorporate the desired foreign gene into the genome of the plant to create a transgenic plant. "It is preferred to produce those pharmaceuticals, which are protein, carbohydrate or lipid based, specifically those which can be expressed and stored in roots, seeds or small inclusion bodies in the cell," explains the Director of Department of Biotechnology (DBT). After the plants are harvested, they go through a series of processing steps that extract, separate, purify and package the therapeutic proteins.
The production of the desired protein in a plant requires a number of complicated molecular biology techniques, where the propriety promoter is fused to the gene of the target protein, forming an expression cassette. With these transgenic techniques, the proprietary expression cassette is introduced into plant cells. The transformed cells are then cultured as suspension cells or regenerated as transgenic plants. High protein expressers are selected and used for protein production. The refined therapeutic proteins are ultimately used as active pharmaceutical ingredients (APIs) in many life-saving medicines and are regulated by the FDA.
In PMPs, plants are the factory or storehouse, where proteins, that will be used in subsequent manufacture of medicines, as the API in a pharmaceutical product, are produced. The normal techniques of extraction, purification and formulation, which are used in normal pharmaceutical companies, are all followed even in the case of PMPs. Though therapeutic proteins produced in PMP field trials are usually not intended to be administered via food, some of the PMPs can be taken orally, while some have to be injected.
Production platforms
There are several plant-based protein production platforms that rely on protein expression from nuclear genes and viral vectors in leaf, seed, tuber and tissue culture cells. However, each of the platforms has its own strengths and weaknesses. Crops such as corn, tobacco, rice, soy, wheat, barley and maize are genetically altered to yield proteins in different parts of the plant. Scientists prefer to opt for genetically modified food crops because of the good understanding of genetics, agronomics and environmental impact of the crops.
Leafy crops are advantageous in terms of biomass yield, but since proteins expressed in such leaves tends to be unstable, the harvested material has a limited shelf life and therefore, must be processed immediately after harvest. However, proteins that are expressed in cereal seeds are protected from proteolytic degradation. Hence, such proteins can be preserved for three years at room temperature and for at least three years at refrigerator temperature without much loss of activity. Prodigene, an industry leader in cereal based protein production has chosen Maize because of its high biomass yield.
Yet another plant group which is considered as good hosts for protein production are oil crops, as oil bodies can be exploited to simplify protein isolation. As per published records, SemBioSys Genetics has developed oleosin-fusion platform, in which the target recombinant protein is produced in oilseed rape as a fusion with oleosin. The Finnish biotech company, Unicrop is also developing an oil seed platform. However, they are attempting to isolate recombinant proteins from rapidly developing sprouts cultivated in bioreactors.
Tobacco helps
Surprisingly, tobacco forms a well-established expression host for which robust transformation procedures are available. Tobacco has a high biomass yield and rapid scalability which makes it a popular choice for commercial molecular farming. "Tobacco is also preferred since it is not a food or feed crop and hence carries reduced fear for transgenic material or recombinant proteins contaminating feed and human food chain," explains Reddy. However, the high content of nicotine and other toxic alkaloids, which are harmful, need to be completely removed during downstream processing steps. Tobacco, as a platform, has also been adopted by several biotech companies, across the world. According to the latest published records, Planet Bio-technology and Meristem Therapeutics are companies who have PMPs with tobacco as a platform with products in Phase II clinical trials.
In the future
Stunning advances in areas of immunology, genomics and molecular screening have dramatically increased the hope for PMPs in the pipeline. But the truth is that the pipeline is not flowing as smoothly as it should because of the daunting costs of building adequate production facilities. "Any new technology is expensive in the beginning but with increase in volumes, competition and time, the price will come down," opines Reddy. Agrees the Director from DBT, "Once the procedures are standardised and streamlined, PMPs can be very cost-effective," she says. She also feels that there is a good potential in the technology but in India, it is not being taken up in an aggressive manner as it has been done in US and France. However, the industry is still optimistic about it.
Researchers believe that one of the keys to success will be the level of expression of the recombinant protein in plants. The expression level will affect the cost of growing, processing, extraction, purification and waste disposal.
