*S Supporting Information ABSTRACT: We report the effects of the interaction of two camelid antibody fragments, generally called nanobodies, namely cAb-HuL5 and a stabilized and more aggregation-resistant variant cAb-HuL5G obtained by protein engineering, on the properties of two amyloidogenic variants of human lysozyme, I56T and D67H, whose deposition in vital organs including the liver, kidney, and spleen is associated with a familial non-neuropathic systemic amyloidosis. Both NMR spectroscopy and X-ray crystallographic studies reveal that cAb-HuL5 binds to the α-domain, one of the two lobes of the native lysozyme structure. The binding of cAb-HuL5/cAb-HuL5G strongl
One of the 20 or so human amyloid diseases is associated with the deposition in vital organs of full...
One of the 20 or so human amyloid diseases is associated with the deposition in vital organs of full...
Systemic amyloidosis is caused by misfolding and aggregation of globular proteins in vivo for which ...
We report the effects of the interaction of two camelid antibody fragments, generally called nanobod...
We report the effects of the interaction of two camelid antibody fragments, generally called nanobod...
Six variants of human lysozyme (single-point mutations I56T, F57I, W64R, D67H and double mutations ...
Six variants of human lysozyme (single-point mutations I56T, F57I, W64R, D67H and double mutations F...
A single-domain fragment, cAb-HuL22, of a camelid heavy-chain antibody specific for the active site ...
A single-domain fragment, cAb-HuL22, of a camelid heavy-chain antibody specific for the active site ...
We report the studies of three new camelid antibody fragments denoted cAb-HuL3, cAb-HuL5, and cAb-Hu...
Amyloid diseases are characterized by an aberrant assembly of a specific protein or protein fragment...
Nanobodies are single chain antibodies that are uniquely produced in Camelidae, e.g. camels and llam...
peer reviewedAmyloid diseases are characterized by an aberrant assembly of a specific protein or pro...
Abstract Nanobodies are single chain antibodies that are uniquely produced in Camelidae, e.g. camels...
Nanobodies are single chain antibodies that are uniquely produced in Camelidae, e.g. camels and llam...
One of the 20 or so human amyloid diseases is associated with the deposition in vital organs of full...
One of the 20 or so human amyloid diseases is associated with the deposition in vital organs of full...
Systemic amyloidosis is caused by misfolding and aggregation of globular proteins in vivo for which ...
We report the effects of the interaction of two camelid antibody fragments, generally called nanobod...
We report the effects of the interaction of two camelid antibody fragments, generally called nanobod...
Six variants of human lysozyme (single-point mutations I56T, F57I, W64R, D67H and double mutations ...
Six variants of human lysozyme (single-point mutations I56T, F57I, W64R, D67H and double mutations F...
A single-domain fragment, cAb-HuL22, of a camelid heavy-chain antibody specific for the active site ...
A single-domain fragment, cAb-HuL22, of a camelid heavy-chain antibody specific for the active site ...
We report the studies of three new camelid antibody fragments denoted cAb-HuL3, cAb-HuL5, and cAb-Hu...
Amyloid diseases are characterized by an aberrant assembly of a specific protein or protein fragment...
Nanobodies are single chain antibodies that are uniquely produced in Camelidae, e.g. camels and llam...
peer reviewedAmyloid diseases are characterized by an aberrant assembly of a specific protein or pro...
Abstract Nanobodies are single chain antibodies that are uniquely produced in Camelidae, e.g. camels...
Nanobodies are single chain antibodies that are uniquely produced in Camelidae, e.g. camels and llam...
One of the 20 or so human amyloid diseases is associated with the deposition in vital organs of full...
One of the 20 or so human amyloid diseases is associated with the deposition in vital organs of full...
Systemic amyloidosis is caused by misfolding and aggregation of globular proteins in vivo for which ...