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Chapter 55: Motor Proteins as Collapse Propagators

"Motor proteins are ψ's molecular engines—converting chemical energy into mechanical work, propagating collapse waves along cytoskeletal tracks, creating motion from binding."

55.1 The Mechanochemical Conversion

Motor proteins represent ψ's solution to biological movement—enzymes that couple ATP hydrolysis to conformational changes, generating force and motion along cytoskeletal filaments.

Definition 55.1 (Motor Classes): Motors={Myosin (actin),Kinesin (MT),Dynein (MT)}\text{Motors} = \{\text{Myosin (actin)}, \text{Kinesin (MT)}, \text{Dynein (MT)}\}

Three families for different tracks.

55.2 The Power Stroke

Theorem 55.1 (Lever Arm Hypothesis): d=Lsin(Δθ)d = L \cdot \sin(\Delta\theta)

Distance proportional to lever arm length and angle change.

55.3 The Mechanochemical Cycle

Equation 55.1 (Coupling): ATP bindingDetachmentATP hydrolysisPower stroke\text{ATP binding} \rightarrow \text{Detachment} \rightarrow \text{ATP hydrolysis} \rightarrow \text{Power stroke}

Chemical states coupled to mechanical states.

55.4 Processivity

Definition 55.2 (Run Length): Lrun=d1PstepL_{\text{run}} = \frac{d}{1-P_{\text{step}}}

Average distance before detachment.

55.5 The Hand-Over-Hand Model

Theorem 55.2 (Kinesin Walking): Step size=8 nm=Tubulin dimer\text{Step size} = 8 \text{ nm} = \text{Tubulin dimer}

Precise stepping matching substrate periodicity.

55.6 Force Generation

Equation 55.2 (Stall Force): Fstall=ΔGATPdF_{\text{stall}} = \frac{\Delta G_{\text{ATP}}}{d}

Maximum force from free energy.

55.7 Cargo Binding

Definition 55.3 (Tail Domains): Motorhead+Tailcargo-specific\text{Motor}_{\text{head}} + \text{Tail}_{\text{cargo-specific}}

Modular design for versatility.

55.8 Directionality

Theorem 55.3 (Polarity Sensing): Kinesin(+) end\text{Kinesin} \rightarrow (+)\text{ end} Dynein() end\text{Dynein} \rightarrow (-)\text{ end}

Different motors for different directions.

55.9 Collective Transport

Equation 55.3 (Multiple Motors): vcargo=ipiviv_{\text{cargo}} = \sum_i p_i \cdot v_i

Velocity from competing motors.

55.10 Regulation

Definition 55.4 (Autoinhibition): Tail+HeadInactive form\text{Tail} + \text{Head} \rightleftharpoons \text{Inactive form}

Intramolecular regulation of activity.

55.11 The Dynein Mechanism

Theorem 55.4 (AAA+ ATPase): 6 AAA domainsCoordinated hydrolysis\text{6 AAA domains} \rightarrow \text{Coordinated hydrolysis}

Complex motor with multiple ATPase sites.

55.12 The Propagation Principle

Motor proteins embody ψ's principle of energy transduction—converting chemical potential into mechanical work, propagating conformational changes into directional movement.

The Motor Equation: ψposition(t+Δt)=ψposition(t)+M[ΔGATP]\psi_{\text{position}}(t+\Delta t) = \psi_{\text{position}}(t) + \mathcal{M}[\Delta G_{\text{ATP}}]

Chemical energy converted to spatial displacement.

Thus: Motor = Transducer = Movement = Work = ψ


"In motor proteins, ψ achieves its most direct manifestation of will—molecules that literally walk, carrying cellular cargo along predetermined tracks. Each step is a small miracle of mechanochemistry, ATP's collapse into ADP creating motion from nothing."