Creation of the spin out company Dundee Cell Products (DCP) and impact on commercialisation of life sciences technology and reagents from the University of Dundee.
Submitting Institution
University of DundeeUnit of Assessment
Biological SciencesSummary Impact Type
TechnologicalResearch Subject Area(s)
Chemical Sciences: Analytical Chemistry
Biological Sciences: Biochemistry and Cell Biology
Summary of the impact
As sophisticated proteomics methodologies are increasingly embraced by
both academics and industry across the globe, growth in this area is set
to explode. The University of Dundee has a leadership position in
quantitative proteomics technology, through the expertise of Professor
Angus Lamond. Dundee Cell Products Ltd is a University of Dundee spin-out
company that was created to commercialise life sciences technology and
reagents, and to exploit technology and expertise in proteomics developed
at the College of Life Sciences. As of 2013, DCP offers >5,000 research
products and six contract research services, centred around quantitative
proteomics.
Underpinning research
In 1998, a seminal study by Prof Angus Lamond FRS at the
University of Dundee, in collaboration with Prof Matthias Mann (then based
in EMBL, Heidelberg), provided insight into proteins that control the
human spliceosome using mass spectrometry (1). This was one of the first
studies to reveal the power of mass spectrometry to biologists and
highlighted the potential of using this technique to simultaneously
identify all or most of the proteins components of human macromolecular
complexes, organelles and cells. In 2000-2001, research by Dr Paul
Ajuh, then a postdoctoral fellow in the laboratory of Prof Lamond,
provided further insight into the composition of the spliceosome complex
and demonstrated the involvement of the CDC5L protein complex in
spliceosome assembly (2,3). In a further subsequent study, Dr Ajuh
identified small peptides that could be used as effective RNA splicing
inhibitors (4).
In 2002, Prof Lamond published a comprehensive analysis of the
composition of the human nucleolus using a range of mass spectrometry
techniques. This work represented a significant advance towards defining a
comprehensive inventory of nucleolar proteins and revealed that the
nucleolus was likely to perform functions beyond its known role at that
time of ribosome subunit biogenesis (5). The ability to purchase large
amounts of reliably high quality subcellular components and extracts was
identified by Dr Ajuh and Prof Lamond as a major rate-limiting step in all
these studies, along with access to appropriate proteomics platforms and
expert data analysis. Prof Lamond and Dr Ajuh created Dundee Cell Products
in 2006 to fill this niche in the market, taking advantage of the
expertise in cell biology, proteomics and mass spectrometry developed in
the University. The main strengths (and selling point) of the company were
to be the quality of their products and the high level of
expertise of the individuals involved in the company.
The rapid evolution in proteomics over the last decade, creating a new
research field whereby the large-scale detection, analysis and
quantitation of proteins has become possible, presented a further
opportunity for Dundee Cell Products. The laboratory of Prof Lamond was
the first in the UK and one of the first worldwide to adopt and develop
quantitative mass spectrometry using stable isotope labeling with amino
acids in cell culture (SILAC). In 2008, Prof Lamond and colleagues
extended the SILAC methods previously reported, and optimised the
technology to produce an unbiased procedure to reliably identify specific
protein interaction partners (6). It was quickly realised that there was
commercial demand for expertise and reagents associated with this powerful
and reliable workflow and as a result, provision of this technology was
adopted in the portfolio of products and services offered by Dundee Cell
Products.
References to the research
Publications:
1. Neubauer, G., King, A., Rappsilber, J., Calvio, C., Watson, M., Ajuh,
P., Sleeman, J., Lamond, A.I. and Mann, M. (1998) Mass
Spectrometry and EST-database searching allows rapid characterization of
the multi-protein spliceosome complex. Nature Genetics 20, 46-50.
(doi: 10.1038/1700) (Citations 339, Scopus Nov 2013)
2. Ajuh, P., Kuster, B., Panov, K., Zomerdijk, J.C.B.M. and Lamond,
A.I. (2000) Functional analysis of the human CDC5L complex and
identification of its components by mass spectrometry. EMBO J. 19,
6569-6581. (doi:10.1093/emboj/19.23.6569) (Citations 110, Scopus Nov 2013)
3. Ajuh, P., Sleeman, J.E., Chusainow, J. and Lamond, A.I.
(2001) A direct Interaction between the Carboxyl-terminal Region of CDC5L
and the WD40 Domain of PLRG1 is Essential for Pre-mRNA Splicing. J.Biol.
Chem. 276, 42370-42381. (doi: 10.1074/jbc.M105453200) (Citations
32, Scopus Nov 2013)
4. Ajuh, P.M. and Lamond, A.I. (2003) Identification of
peptide inhibitors of pre-mRNA splicing derived from the essential
interaction domains of CDC5L and PLRG1. Nucl. Acids Res. 31,
6104-6116 (doi: 10.1093/nar/gkg817) (Citations 9, Scopus Nov 2013)
5. Andersen, J.S., Lyon, C.E., Fox, A.H., Leung, A.K.L., Lam, Y.W.,
Steen, H., Mann, M. and Lamond, A.I. (2002) Directed Proteomic
Analysis of the Human Nucleolus. Curr. Biol. 12, 1-11. (doi
10.1016/S0960-9822(01)00650-9) (Citations 559, Scopus Nov 2013)
6. Trinkle-Mulcahy, L., Boulon, S., Lam, Y.W., Urcia, R., Boisvert, F-M.,
Vandermoere, F. Morrice, N.A., Rothbauer, U., Leonhardt, H., and Lamond,
A.I. (2008) Identifying specific protein interaction partners using
quantitative mass spectrometry and bead proteomes. Journal of Cell
Biology. 183, 223-239. (doi: 10.1083/jcb.200805092)
(Citations 151, Scopus Nov 2013)
Key research grants relevant to this case study:
1. Human Frontiers Science Programme (2001) Functional Organization of
the Cell Nucleus Investigated Through Proteomics and Molecular Dynamics.
Value: £137,652. Grant Ref. rgp0031/2001-m. Principal Grant Holder: A I
Lamond
2. MRC grant (2004) Proteomic Analysis of the Function of Nuclear SUMO
Modification. Value: £424,220. Grant Ref. G0301131. Principal Grant
Holder: A I Lamond
3. Wellcome Trust Programme Grant (2005) Structure and function of the
mammalian cell nucleus. Value: £3,121,320. Grant Ref. 073980/Z/03/B.
Principal Grant Holder: A I Lamond
4. Wellcome Trust Strategic Award (2007): Centre for Gene Regulation and
Expression. Value: £4,997,609 Grant Ref. 083524/Z/07/Z. Principal Grant
Holder: A I Lamond.
5. EU FP7 Prospects network grant (2008) PROteomics SPECification in Time
and Space (PROSPECTS). Value: 1,046,019 Euros Grant Ref.
HEALTH-F4-2008-201648. Principal Grant Holder: A I Lamond
6. Wellcome Trust Principal Research Fellowship (2009) Structure and
function of the mammalian cell nucleus. Value: £3,113,288 Grant Ref.
073980/Z/03/B. Principal Grant Holder: A I Lamond.
Details of the impact
Beneficiaries
(a) UK and local Dundee Biotech (by introducing new cutting-edge
technology services into the sector).
(b) Pharma and Biotech companies (such as Pfizer) using mass spectrometry
and other services provided by DCP.
(c) Academic translational programs using mass spectrometry and other
services provided by DCP.
Dundee Cell Products (DCP) is an innovative SME commercialising high
quality research tools for life sciences research (http://www.dundeecellproducts.com).
Moreover, it provides services to pharmaceutical and biotechnology
companies as well as to academic researchers.
DCP was formed in 2006 by Prof Lamond and Dr Ajuh (who became Chief
Scientific Officer and Chief Executive Officer respectively) with
co-investment and assistance from the University of Dundee. In 2007, the
company secured equity investment funding from a syndicate of angel
investors to finance and expand its activities, followed in 2009 by
a six-figure investment from angel investors and the Scottish
Co-investment Fund (SCF). This helped DCP establish manufacturing and
research facilities, and recruit expert technical and sales staff to
expand its product portfolio. In 2011, Dundee Cell Products was awarded a
£70,000 SMART:Scotland award from Scottish Enterprise (1). This award
supported the development of proteomic-based methods in predictive
toxicology. This was also accompanied by a £20,000 BioKT R&D grant by
the Innovation Portal Dundee to develop new human growth factor products
and related services (1).
Since its launch in 2006, DCP's turnover has increased ~10 fold and the
company broke even in 2010. As of 2013, the company employed 10 people
(eight with PhDs) with plans to increase headcount to 15-20 by 2015 with
the development of novel high technology products and services. During the
assessment period, turnover on the company's core products and services
has been growing at ~30% year on year (2). Since 2008, the company has
greatly expanded its products and services catalogue and as of 2013 offers
>5,000 products and six contract research services. Moreover, the
company has built SILAC-based quantitative proteomics, SILAQTM,
as one of its innovative contract research services as a direct result of
expertise at the University of Dundee.
DCP has successfully completed commercial contracts with both biotech and
major pharma companies. In 2013, ~30% of its income came from
international sales to countries including: Italy, Spain, France, Germany,
Switzerland, Sweden, Belgium, Hong Kong, Japan, the USA and Malaysia. Two
examples of commercial partnerships are:
- In 2009, DCP signed a major contract research agreement with Pfizer to
develop new SILAQ applications to facilitate the discovery and
development of new and safer drugs, potentially saving millions of
dollars of clinical trial costs (3). This agreement was renewed in 2010.
- In 2008, DCP announced a major partnership deal with the biotechnology
company Molecular Targeting Technologies, Inc (MTTI) (http://www.mtarget.com)
(4). Under this agreement, DCP has the rights to distribute a portfolio
of MTTI products in Europe primarily based upon fluorescence research
applications.2028
DCP also provides services to academic clients. As of 2013, the company
had contracts with >70 Universities worldwide (2). For example, DCP has
been involved in projects with the University of Leeds to investigate the
effects of virus infections on cellular proteomes (5) and with the Paul
Ehrlich Institute, Germany to study molecular mechanisms of transmissible
spongiform encephalopathies (6).
The company maintains a close working relationship with the University of
Dundee and other UK Universities. For example DCP has been involved in
five CASE studentships over the assessment period: 4 MRC-CASE PhD
studentships together with academics at the Universities of Aberdeen,
Dundee, Imperial College London and St Andrews and a BBSRC-CASE PhD
studentship with the Roslin Institute, Edinburgh. For these studentships
DCP provides training in research technologies and in their
commercialisation. The company also benefits from continued links with the
Lamond laboratory and when appropriate can utilise specialist equipment at
the University. From 2010-2013 DCP was engaged in a DTI / Scottish
Executive sponsored Knowledge Transfer Partnership with other mass
spectrometry researchers in the College of Life Sciences (Dr Dougie Lamont
and Prof Julian Blow) (7). DCP has been able to recruit highly skilled
staff from the College of Life Sciences, providing jobs for postgraduate
and postdoctoral researchers from the University. This highlights the
economic opportunity provided by the College of Life Sciences creating a
highly trained local pool of life scientists with skills that are of
direct benefit to biotechnology companies. Moreover, DCP has provided an
outlet for the commercialisation of new products and services in cutting
edge proteomics initially derived at the University.
Sources to corroborate the impact
- Press release regarding SMART Scotland award from Scottish Enterprise
for the development of a quantitative proteomics screening assay for
predictive toxicology and BioKT R&D award from the Innovation Portal
http://www.innovationportal.co.uk/news/news/2011/11/25/282.html
- Confidential corroboration of the size/revenue of the company can be
obtained from the Executive Director of Dundee Cell Products, Dundee
Technopole,2028Dundee, DD1 5JJ. Other data can be found at www.dundeecellproducts.com/
- Announcement of contract research partnership with Pfizer
http://www.dundeecellproteomics.com/latest-news
- Announcement of partnership with Molecular Targeting Technologies,
Inc.
http://www.mtarget.com/mtti/whatsnew/DundeeMTTI08Aug22.pdf
- Collaboration with the Institute of Molecular and Cellular Biology,
Faculty of Biological Sciences, University of Leeds: Emmott, E.,
Rodgers, M.A., and Macdonald, A., McCrory, S., Ajuh, P. and Hiscox, J.A.
(2010) Quantitative proteomics using stable isotope labeling with amino
acids in cell culture reveals changes in the cytoplasmic, nuclear, and
nucleolar proteomes in Vero cells infected with the coronavirus
infectious bronchitis virus. Mol Cell Proteomics. 9, 1920-1936.
(doi: 10.1074/mcp.M900345-MCP200)
- Collaboration with the Paul Ehrlich Institute, Germany: Wagner, W.,
Ajuh, P., Löwer, J and Wessler, S. (2010) Quantitative phosphoproteomic
analysis of prion-infected neuronal cells. Cell Comm and Signaling. 8,
28. (doi: 10.1186/1478-811X-8-28)
- Details of the Knowledge Transfer Partnership are available at
http://info.ktponline.org.uk/action/details/partnership.aspx?id=7902