Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UMLS:C0002962 (
angina
)
21,142
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Heparin cofactor II
(
HCII
) is a serine proteinase inhibitor in human plasma that rapidly inhibits thrombin in the presence of dermatan sulfate or heparin. To understand the molecular mechanism for
HCII
deficiency in a patient with reduced circulating
HCII
antigen, we studied a Japanese patient with type I
HCII
deficiency who suffered from
angina pectoris
and coronary artery disease. Polymerase chain reaction (PCR)-based sequence analysis showed that the propositus' gene for
HCII
(
HCII
Awaji gene) had a thymine insertion after codon (GAT) for Asp88 in exon II, resulting in a frameshift mutation. Consequently, the abnormal
HCII
Awaji protein was suggested to have an altered amino acid sequence from position 89 and terminate at 107, thus being composed of the NH2-terminal one fifth of normal
HCII
and dysfunctional for thrombin inhibition. The molecular weight and pI value of
HCII
Awaji were calculated to be 12,040 and 3.6, respectively, without posttranslational modification. Mutagenic PCR followed by the Tsp509I digestion showed that a half of the PCR products derived from the propositus and his sister was cleaved, suggesting that his sister also has the same mutant allele. Crossed-immunoelectrophoresis and Western blot analyses of plasma and urine from the the propositus and of plasma from his sister did not provide evidence for the existence of the abnormal
HCII
, suggesting that little truncated
HCII
was circulating in the patient's blood. However, stable expression assay using human kidney 293 cells transfected with the expression vector containing cDNA encoding wild-type or Awaji-type
HCII
showed that mutant as well as wild-type
HCII
was secreted into culture medium normally. These results suggest that the abnormal
HCII
Awaji protein is secreted normally, but rapidly degraded in the circulating blood.
...
PMID:Molecular and cellular basis for type I heparin cofactor II deficiency (heparin cofactor II Awaji). 856 24