Natural Killer (NK) Cell Cytotoxicity

The Calvin cycle, or light-independent reactions, uses the ATP and NADPH produced during the light-dependent stage to convert inorganic carbon dioxide into organic sugar molecules. This process occurs in the stroma of the chloroplast. The key enzyme, RuBisCO, catalyzes the first step: the fixation of \(CO_2\) into an organic molecule, initiating a cycle that produces carbohydrates.

Translation is the biological process in which ribosomes in the cytoplasm or endoplasmic reticulum synthesize proteins. It follows transcription, where the DNA sequence is copied into a messenger RNA (mRNA) molecule. During translation, the ribosome reads the mRNA sequence in three-nucleotide units called codons, and with the help of transfer RNA (tRNA), assembles the corresponding amino acid chain.

SAL is a quantitative measure representing the probability of a single viable microorganism surviving on an item after sterilization. A commonly required SAL for medical devices is \(10^{-6}\), meaning a one-in-a-million chance of a non-sterile unit. This probabilistic approach acknowledges that absolute sterility cannot be proven, only inferred statistically from process validation.

Biomimicry is an innovation approach that seeks sustainable solutions to human challenges by emulating nature's time-tested patterns and strategies. The core idea is that nature, through 3.8 billion years of evolution, has already solved many of the problems we are grappling with. It involves observing and learning from the designs and processes of organisms and ecosystems to create more sustainable designs.

Cytotoxicity is the quality of a substance or cell being toxic to other cells. Cytotoxic agents can induce cell death through necrosis, where the cell membrane loses integrity leading to lysis and inflammation, or apoptosis, a controlled, programmed cell death process. This is distinct from cytostatic agents, which only inhibit cell division without directly causing cell death.

The alpha-helix (\(\alpha\)-helix) is a common secondary structure motif in proteins. It is a right-handed coiled conformation in which every backbone N-H group donates a hydrogen bond to the backbone C=O group of the amino acid located four residues earlier (\(i+4 \rightarrow i\) hydrogen bonding). This regular pattern pulls the polypeptide chain into a helical shape.

Insulin is synthesized in pancreatic beta cells as a single-chain precursor called proinsulin. In the endoplasmic reticulum, proinsulin folds and forms its disulfide bonds. It is then transported to the Golgi apparatus and packaged into secretory granules, where proteases (prohormone convertases PC1/3 and PC2, and carboxypeptidase E) cleave it into mature insulin and a connecting peptide, C-peptide.

Recombinant DNA (rDNA) technology involves joining together DNA molecules from two different species. The recombinant DNA is inserted into a host organism to produce new genetic combinations. This is achieved using restriction enzymes to cut DNA at specific sites and DNA ligase to join the fragments, often incorporating the desired gene into a plasmid vector for cloning.

The MTT assay is a colorimetric method for assessing cell metabolic activity, which serves as a proxy for cell viability, proliferation, and cytotoxicity. Viable cells with active mitochondria contain reductase enzymes that convert the yellow tetrazolium salt MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) into an insoluble purple formazan. The amount of formazan produced is proportional to the number of living cells.

Insulin initiates its effects by binding to the insulin receptor (IR), a receptor tyrosine kinase. This binding triggers autophosphorylation of the receptor, creating docking sites for insulin receptor substrate (IRS) proteins. Phosphorylated IRS proteins then activate downstream pathways, primarily the PI3K/Akt pathway, which mediates most of insulin's metabolic effects, including the translocation of GLUT4 glucose transporters to the cell membrane.