Skip to content
Skip to navigation menu

 

Dr Carlo Knupp 


Staff Photos
Position:Senior Research Fellow

Telephone:+44 (0)29 2087 0118
Fax:+44 (0)29 2087 4859
Extension:70118
Location:Room 3.09, Maindy Road

My main research interest is to understand the molecular organisation of “fibrous proteins”, in particular that of collagens forming networks and that of the proteins in the muscle sarcomere.

Network forming collagens do not form fibrils, but their general role appears to be to provide both mechanical strength and filtering properties. In some cases the open networks that they form are ordered enough that their structure can be analysed both by X-ray diffraction and by electron microscopy to reveal the basic molecular packing arrangements. I have taken advantage of the remarkably good order in the network-like structure of the egg case walls of the dogfish to reveal an open, body-centred, collagen molecular assembly. Intriguingly, something similar to this has been found in the human eye associated with a condition known as full thickness macular holes. In this case it appears to be collagen Type VI that is forming the aggregates. I am continuing to explore the nature of such collagen aggregates in the eye, especially in relation to Sorsby’s Fundus Dystrophy and Age-Related Macular Degeneration. I also carry out theoretical analyses of collagen amino acid sequences to try to understand the general principles that link collagen structures and functions. 

The cornea is another system where collagen is organised as a network that possesses incredible optical properties. My aim is to understand which physical mechanisms are responsible for this organisation and how corneal optical properties arise. At present we are pursuing this by means of three-dimensional electron microscopy.

In collaboration with the Cell Signalling and Cell Biology Section at the University of Bristol, I am studying the ultrastructure of the myosin and actin filaments using X-ray fibre diffraction. In particular, we are following dynamic molecular changes in active muscle by means of fast (millisecond) time-resolved X-ray diffraction using very powerful X-ray beams from synchrotron X-ray sources, particularly the Advance Photon Source, at Argonne National Laboratory, in the US.