http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2010529008-A
Outgoing Links
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|---|---|
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| classificationIPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/H01J37-20 |
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| filingDate | 2008-04-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2010-08-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-2010529008-A |
| titleOfInvention | Protein layers and their use in electron microscopy |
| abstract | A two-dimensional regularly repeating protein layer (1) is a protein protomer (2) comprising at least two monomers (5), (6), each genetically fused together including. Monomers (5) and (6) are the monomers of the respective oligomer aggregates (3) and (4). The monomers aggregate to construct an oligomer aggregate, and the assembly of protein layers Build the body. The first oligomer assembly (3) belongs to a dihedral point group of order O, where O is equal to (3), (4) or (6). It has a rotational symmetry axis. The second oligomer assembly (4) has a rotational symmetry axis of order (2). Due to the symmetry of the oligomer assembly (3), (4), the rotational symmetry axis of each of the second oligomer assembly (4) is the O rotational symmetry of the set of the first oligomer assembly (3). Aligned in line with one of the axes, the protomer of (2) is placed symmetrically around it. Therefore, a fusion in two directions is generated between the oligomer assemblies (3) and (4), and the protein layers are regularly repeated due to the arrangement of the rotational symmetry axes of the oligomer assemblies (3) and (4). To do. Protein layers have many uses and support molecular entities for biosensing, X-ray crystallography or electron microscopy, for example. [Selection] Figure 1 |
| priorityDate | 2007-05-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
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