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Volume 6, Issue 4 (Suppl)

J Material Sci Eng, an open access journal

ISSN: 2169-0022

Materials Congress 2017

June 12-14, 2017

Page 32

conference

series

.com

June 12-14, 2017 Rome, Italy

Materials Science and Engineering

9

th

World Congress on

Robert Huber, J Material Sci Eng 2017, 6:4(Suppl)

DOI: 10.4172/2169-0022-C1-066

New ways of vision: Protein structures in translational medicine and business development - My

experience

A

s a student in the early nineteen sixties, I had the privilege to attend winter seminars organized by my mentor, W Hoppe,

and by M Perutz, which took place in a small guesthouse in the Bavarian, Austrian Alps. The entire community of a

handful of protein crystallographers assembled in a room which served as living and dining room and as auditorium for the

lectures. Today structural biologists organize large congresses with thousands of attendants and there exist many hundreds

of laboratories specialized in this field. It appears to dominate biology and biochemistry very visibly if we count covers

in scientific journals displaying macromolecular structures. Structural biology was successful, because it was recognized

that understanding biological phenomena at the molecular and atomic level requires seeing those molecules. Structural

biology revealed the structure of genes and their basic mechanism of regulation, the mechanism of enzymes’ function, the

structural basis of immune diversity, the mechanisms of energy production in cells by photosynthesis and its conversion into

energy- rich chemical compounds and organic material, the mechanism that makes muscle work, the architecture of viruses

and multi-enzyme complexes, and many more. New methods have an essential impact on the development of structural

biology. Methods seem to become available in cadence with the growing complexity of the problems and newly discovered

methods bring biological problems within reach for researchers, a co-evolutionary process of the development of methods and

answerable problems, not only in the field of X-ray diffraction, but also in optical microscopy, nuclear magnetic resonance,

and electron microscopy. An important additional incentive for structural biology came from its potential application for drug

design and development using knowledge of drug receptor structures at the atomic level combined with theoretical approaches

of ligand binding. The commercial interest in application spurred this direction of research enormously. My lecture will focus

on protein crystallography and start out with the major factors contributing to its development. Few examples shall illustrate

how structure information contributes to our understanding of the physical and chemical basis of biological phenomena

and may lead to medical application. I then will let you share my experience with the foundation and development of two

biotech companies with different business models, but both based on basic academic research in structural biology: Proteros

(www.Proteros.com

) offers enabling technology services for pharma- and crop science companies imbedding all steps of the

workflow molecular and structural biology can provide and commands and uses its platform for the generation of leads from

identified targets to in vivo Proof-of-Concept (PoC). Suppremol

(www.Suppremol.com

) specializes in the development of

novel immune-regulatory therapeutics for the treatment of autoimmune diseases on the basis of a recombinant, soluble, non-

glycosylated version of the human Fcg receptor IIB and of receptor binding antibodies. Suppremol was recently acquired by

Baxter International Inc. (NYSE:BAX) offering an ideal setting for its therapeutic projects.

Biography

Robert Huber is Director at the Max Planck Institute for Biochemistry, where his team developed methods for the crystallography of proteins. In 1988, he received the Nobel

Prize for Chemistry jointly with Johann Deisenhofer and Hartmut Michel. Three were recognized for their work in first crystallizing an intra-membrane protein important in

photosynthesis in purple bacteria, and subsequently applying X-ray crystallography to elucidate the protein's structure. The information provided the first insight into the

structural bodies that performed the integral function of photosynthesis. This insight could be translated to understand the more complex analogue of photosynthesis in

cyanobacteria which is essentially the same as that in chloroplasts of higher plants. In 2006, he took up a post at the Cardiff University to spearhead the development of

structural biology at the university on a part-time basis. Since 2005, he has been doing research at the Center for Medical Biotechnology of the University of Duisburg-Es-

sen. He was one of the original editors of the “

Encyclopedia of Analytical Chemistry

”.

huber@biochem.mpg.de

Robert Huber

1,2,3

1

Max Planck Institute of Biochemistry, Germany

2

Technical University of Munich, Germany

3

University of Duisburg-Essen, Germany