Cell Division Stimulation
Specific proteins, such as epidermal growth factor (EGF), stimulate cell division and growth.
EGF receptors pair with protein tyrosine kinases for signal transduction.
G Proteins
G proteins are crucial in signal transduction; they mediate the exchange of GDP for GTP to activate the signaling cascade for cell growth.
When activated, G proteins lead to the growth of epidermal tissue for functions such as healing wounds or replacing damaged cells.
Mutations or improper activation of G proteins and tyrosine kinases can lead to uncontrolled cell proliferation, often correlated with cancer development.
The inactive state has GDP attached, while the active state has GTP, indicating a switch in activity.
If GTP cannot be hydrolyzed back to GDP, active signaling continues leading to excessive cell growth.
Uncontrolled Cell Growth
Cancer cells often result from g protein signaling being constantly active due to lack of regulation (inability to revert back to inactive state).
Consequences include the formation of tumors and masses of cells.
Apoptosis
The programmed cell death mechanism prevents damaged or infected cells from spreading harm to other cells.
Key triggers of apoptosis include detachment from the extracellular matrix and damage signaling.
Important during stages like embryonic development and as a defense mechanism against cancerous cells.
Extracellular Matrix (ECM)
Cells attached to ECM receive constant signals indicating they are healthy and continue to grow.
Detaching cells may induce apototic pathways due to unfavorable conditions.
Paracrine Signaling and Yeast Growth
Yeast cells release a signaling molecule called mating factor to induce a different growth cycle in neighboring yeast.
This form of signaling is localized and affects only surrounding cells.
Autoinducers
Bacterial cells release autoinducers to communicate density to surrounding bacteria.
In low density, the signal does not provoke a strong response; in high density, it triggers a positive feedback loop promoting collective behaviors (e.g., toxin production).
Amplified Behavior
When bacteria sense a high density of their kind, they ramp up production of autoinducers which encourages cooperation and actions like toxin secretion to enhance survival and resource exploitation.
Glycolysis
Divided into two phases: the energy-requiring phase (first half) and the energy-releasing phase (second half).
Important for understanding metabolic efficiency and energy extraction from glucose.
Pyruvate to Acetyl CoA
During conversion, carbon is removed, indicating the decarboxylation step that links glycolysis to the citric acid cycle.
Proton Gradient
Energy released from electronic transfer generates a proton gradient across the mitochondrial membrane, driving ATP synthesis via chemiosmosis.
Single plants exposed to various light colors show differential absorption; chlorophyll reflects green light and absorbs blue and red effectively.
Calvin Cycle Activation
Requires carbon dioxide and regenerates key intermediates (e.g., RuBP) to sustain photosynthesis.
Upon bacterium ingestion, white blood cells release chemical messengers that initiate inflammation response proteins synthesis by the liver.
G Protein Activation
Active when GTP is bound; inability to hydrolyze GTP means a protracted active state leading to amplified immune responses.