Truncated fragments of alpha-synuclein in Lewy body disease
The application identifies novel fragments of alpha-synuclein in patients with Lewy Body Disease (LBD) and transgenic animal models thereof. These diseases are characterized by aggregations of alpha-synuclein. The fragments have a truncated C-terminus relative to full-length alpha-synuclein. Some fragments are characterized by a molecular weight of about 12 kDa as determined by SDS gel electrophoresis in tricine buffer and a truncation of at least ten contiguous amino acids from the C-terminus of natural alpha-synuclein. The site of cleavage preferably occurs after residue 117 and before residue 126 of natural alpha-synuclein. The identification of these novel fragments of alpha-synuclein has a number of application in for example, drug discovery, diagnostics, therapeutics, and transgenic animals.
1. A method of screening for an agent having a pharmacological activity useful for treating a Lewy Body Disease (LBD) comprising:
contacting the agent with a fragment of alpha synuclein, which is SN1-115, SN1-133 or SN 1-135, with residues-defined by SEQ ID NO:1 or a hereditary variant thereof associated with Lewy body disease, or an induced variant thereof selected from the group consisting of E83Q, A90V and A76T;
determining the rate or extent of aggregation of the alpha synuclein or fragment of alpha-synuclein, wherein a reduction in the rate or extent of aggregation relative to a control lacking the agent indicates the agent has the pharmacological activity.
2. The method of claim 1 , wherein the fragment of alpha-synuclein bears a hereditary variant associated with a hereditary LBD.
3. The method of claim 2 , wherein the hereditary variant is an A53T mutation, an A30P mutation, an E46K mutation, or any combination thereof.
4. The method of claim 1 wherein the hereditary variant is an A53T mutation.
5. The method of claim 1 , further comprising conducting a trial in a human having a LBD or an animal model of LBD to determine whether the agent treats or inhibits a symptom of the LBD.
6. A purified fragment of alpha synuclein, which is SN1-115, SN1-133 or SN 1-135, with residues defined by SEQ ID NO:1 or a hereditary variant thereof associated with Lewy Body disease, or an induced variant thereof selected from the group consisting of E83Q, A90V and A76T.
7. The purified fragment of claim 6 , wherein the fragment of alpha-synuclein bears a hereditary variant associated with a hereditary LBD.
8. The fragment of claim 7 , wherein the hereditary variant is an A53T mutation, an A30P mutation, an E46K mutation, or any combination thereof.
9. A fragment of alpha synuclein which is SN1-115, SN1-133 or SN 1-135, with residues defined by SEQ ID NO:1, or a hereditary variant thereof associated with Lewy body disease, or a or an induced variant thereof selected from the group consisting of E83Q, A90V and A76T, which fragment is recombinantly expressed or synthesized by solid phase peptide synthesis.
10. The fragment of claim 9 , wherein the fragment of alpha-synuclein bears a hereditary variant associated with a hereditary LBD.
11. The fragment of claim 10 , wherein the hereditary variant is an A53T mutation, an A30P mutation, an E46K mutation, or any combination thereof.