Motor Proteins and Muscles Flashcards

1
Q

Movement

A

The ability to move requires a firm structure to provide leverage and a mechanism for moving that structure; these structures rely on both MOTOR PROTEINS and components of the CYTOSKELETON:
- Multicellular: skeleton and muscle
- Unicellula: flagella and/or cilia

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2
Q

Cytoskeleton

A

cell skeleton; network of filaments that support the PM, gives the cell an overall shape, aids in correct positioning of organelles, provides tracks for vesicle transport, and allows cells to move
- In eukaryotes, there are three types of protein fibers in the cytoskeleton: MICROFILAMENTS, INTERMEDIATE FILAMENTS, MICROTUBULES
- serve as tracks for movement of motor proteins, which use ATP to “walk along” cytoskeletal filaments (microfilaments and microtubules)

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3
Q

Microfilaments

A

AKA actin filaments because they are composed of ACTIN PROTEIN SUBUNITS; serve as tracks for the motor protein MYOSIN and are involved in many cellular processes that require motion
- Form SACROMERES in muscle cells
- when actin and myosin filaments of a sarcomere slide past each other, muscles contract

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4
Q

Sacromere

A

organized structures of overlapping filament made up of microfilaments

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5
Q

Microtubules

A

made up of tubulin proteins and serve as tracks for motor proteins KINESIN + DYNEIN; play roles in cellular structural integrity and cell movement
- cell movement via cilia and flagella

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6
Q

Motor Protein

A

use ATP to “walk” along specific cytoskeletal tracks; essential for movement of vesicles and other cargoes within cells, as well as for the movement of muscles and cilia/flagella
- Myosin
- Dynein
- Kinesin

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7
Q

Myosin

A

actin microfilaments; requires for movement of MUSCLE

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8
Q

Dynein

A

tubulin microtubules; required for movement of CILIA/FLAGELLA

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9
Q

Kinesin

A

tubulin microtubules; required for movement of VESICLES + OTHER INTRACELLULAR CARGOES

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10
Q

Cilia + Flagella

A

Structures essential for movement of eukaryotic cilia and flagella:
- ATP
- Dynein motor proteins
- microtubule tracks

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11
Q

Flagella

A

long, hair-like structures that extend from the cell surface and are used to move an entire cell
- Eukaryotic flagella have different structures and have an independent evolutionary origin from prokaryotic flagella
- EX: Sperm

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12
Q

Cilia

A

shorter, similar to flagella, usually appear in large numbers on the cell surface
- when cells with motile cilia form tissues, the beating helps move materials across the tissue surface
- EX: cilia of cells in upper respiratory system move dust and particles out through the nostriles

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13
Q

Common Structure: Cilia + Flagella

A
  • 9 pairs of microtubules arranged in a circle, with 2 additional ones in the center (9+2 ARRAY)
  • the individual microtubule pairs are physically connected via protein bridges and to the base of the cilium/flagella
  • the movement of dynein motor proteins cause the beating of the flagella/cilia
  • dynein causes the cell to move in a coordinated fashion
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14
Q

TYPES OF MUSCLEEEEEEEEEEEE

A
  • Skeletal Muscles
  • Smooth Muscles
  • Cardiac Muscles
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15
Q

Structures Essential for Muscle

A
  • ATP
  • Myosin motor proteins
  • actin microfilament
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16
Q

Skeletal Muscles

A

attach to bones/skin and control locomotion and any movement that can be consciously controlled; also called VOLUNTARY MUSCLES
- long, cylindrical; stripped/striated appearance
- the striations are caused by the regular arrangement of contractile proteins (actin + myosin)

17
Q

Smooth Muscles

A

occurs in the walls of hollow organs; has no striations, is under automatic control - INVOLUNTARY MUSCLE
- EX: stomach, intestines, bladder, respiratory tract, blood vessels

18
Q

Cardiac Muscle

A

found ONLY in the heart; is striated and cannot be consciously controlled (INVOLUNTARY MUSCLE)
Cardiac contractions pump blood throughout the body and maintain blood pressure
- The heart can beat without the nervous system’s input due to PACEMAKER CELLS that spontaneously initiate cardiac muscle contraction
- has INTERCALATED DISKS, which enable rapid passage of AP from one cardiac muscle cell to the next

19
Q

Skeletal Muscle Structure

A

each skeletal muscle cell is called a MUSCLE FIBER; structures/molecules important in muscle contraction are:
- Myofibrils
- Sarcomeres
- Myosin
- Actin
- Tropomyosin
- Troponin

20
Q

Myofibrils

A

long, cylindrical structures that lie parallel to the muscle fiber; run the entire length of the muscle fiber
- composed of many sarcomeres running along its length, and as they individually contracct, the myofibrils and muscles cells shorten

21
Q

Sarcomere

A

Functional units that make up myofibril that cause contraction of a muscle (contractile units)
- give muscle its striated/banded appearance due to the alternating bands of actin + myosin that allow them to contract
- ACTIN AND MYOSIN COMPONENTS

22
Q

Sarcomere Structure

A

Each one contains a thick, dark filament of myosin and a thin, light filament of actin
- actin filaments are physically anchored to structures at the end of each sarcomere (Z DISCS)
- the center of the myosin filament is marked by an M-Line
- One sarcomere is the space between 2 consecutive Z-Discs
- THE ACTIN + MYOSIN FIBERS STAY THE SAME LENGTH BY SLIDING PAST EACH OTHER AS THE CELL ITSELF SHORTENS

23
Q

Myosin

A

the primary component of thick filaments
- the tail of the myosin molecule connects with the other myosin molecules to form a central region of a thick filament near the M-Line
- the heads align on either side of the filament where the thin filaments overlap

24
Q

Actin

A

the primary component of thin filaments
- attached at the Z-Disc and extend toward the M-Line, overlapping with the myosin heads of the thick filament

25
Tropomyosin
actin has binding sites for myosin attachment, but strands of this block the binding sites and prevent actin-myosin interactions when muscles are at rest
26
Troponin
regulates tropomyosin - regulated by calcium ions - calcium binding to troponin causes the troponin-tropomyosin complex to move away from the myosin binding sites on actin filament, allowing myosin to bind to actin to initiate muscle contraction
27
Muscle Contraction
- for a muscle cell to contract, the sarcomere must shorten - thick and thin filaments of the sarcomere DO NOT shorten, but rather SLIDE by each other, causing the sarcomere to shorten while the filaments remain the same length - AKA Sliding Filament Model
28
Sliding Filament Model
explains the movement of the bands on the sarcomere at different degrees of muscle contraction + relaxation - the mechanism of contraction is the binding of myosin to actin, forming cross-bridges that generate filament movement - the sliding filament is accomplished by the CROSS-BRIDGE CYCLE of actin-myosin binding
29
Cross-Bridge Cycle
when the sarcomere shortens, the distance between Z-discs is reduced even though filaments stay the same length (the thick filament is pulled to the sarcomere center until the Z-discs approach the thick filaments)
30