TY - JOUR
T1 - SPECIFIC CHEMICAL DISSOCIATION OF FIBRILLAR AND NON-FIBRILLAR COMPONENTS OF AMYLOID DEPOSITS
AU - Hind, C. R.K.
AU - Caspi, D.
AU - Collins, P. M.
AU - Baltz, M. L.
AU - Pepys, M. B.
N1 - Funding Information:
North of England Cancer Campaign for financial support.
PY - 1984/8/18
Y1 - 1984/8/18
N2 - In systemic amyloidosis, a fatal disorder for which there is no effective treatment, the extracellular protein deposits are composed of amyloid fibrils together with a non-fibrillar glycoprotein, amyloid P component (AP). Methyl 4,6-O-(1-carboxyethylidene)-β-D- galactopyranoside (MOβDG), a recently identified ligand for AP, was tested for its ability to produce in-vitro elution of AP which had been laid down with amyloid fibrils in vivo. Millimolar concentrations of MOβDG completely dissociated AP from human and murine splenic amyloid deposits. Availability of this material thus provides for the first time the opportunity for specific molecular dissection of amyloid deposits. If MOβDG or a related substance were effective in vivo it might be of therapeutic importance.
AB - In systemic amyloidosis, a fatal disorder for which there is no effective treatment, the extracellular protein deposits are composed of amyloid fibrils together with a non-fibrillar glycoprotein, amyloid P component (AP). Methyl 4,6-O-(1-carboxyethylidene)-β-D- galactopyranoside (MOβDG), a recently identified ligand for AP, was tested for its ability to produce in-vitro elution of AP which had been laid down with amyloid fibrils in vivo. Millimolar concentrations of MOβDG completely dissociated AP from human and murine splenic amyloid deposits. Availability of this material thus provides for the first time the opportunity for specific molecular dissection of amyloid deposits. If MOβDG or a related substance were effective in vivo it might be of therapeutic importance.
UR - http://www.scopus.com/inward/record.url?scp=0021210903&partnerID=8YFLogxK
U2 - 10.1016/S0140-6736(84)90544-0
DO - 10.1016/S0140-6736(84)90544-0
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AN - SCOPUS:0021210903
SN - 0140-6736
VL - 324
SP - 376
EP - 378
JO - The Lancet
JF - The Lancet
IS - 8399
ER -