Criado por Emma Allde
mais de 8 anos atrás
|
||
Questão | Responda |
Sickle cell disease is due to which mutation resulting in abnormally folded haemoglobin (HbS) | Glu -> Val |
The misfolded HbS results in what characteristic | Polymerisation |
Polymerised haemoglobin have what characteristics | Crystallised chain structures which disrupt the membrane of red blood cells |
Alzheimer's disease is mostly likely the result of what | formation of stable aggregations of proteins and amyloid proteins forming plaques |
Creutzfeldt-Jakob's disease is the result of what | stable aggregations of proteins called prions |
What is a prion | A protein that can fold in multiple, structurally distinct ways, at least one of which is transmissible to other prion proteins |
Where are proteins found | on the surface of cells |
Prion protein polymerisation results in conversion of normal PrPC into what | pathogenic form PrSC |
Polymerisation of the pathogenic form (PrPSC) in CJD forms what | fibrils (aggregates) |
Structure of normal prion proteins (PrPC) | Alpha helical, susceptible to proteolysis |
Structure of pathogenic prion proteins (PrPSC) | Beta sheet becomes present, protease resistant so it accumulates Identical amino-acid sequence to normal prion protein |
Neurological symptoms of CJD (5) | Difficulties with walking, slurred speech, numbness, dizziness, visual problems |
Psychological symptoms of CJD (5) | Severe depression, withdrawal, anxiety, irritability, insomnia |
Quer criar seus próprios Flashcards gratuitos com GoConqr? Saiba mais.