Tue, Dec 8, 2026Fall (Semester 1) · Week 16Day 69 of 7280-min blockCalendar fit

Purification overview

Essential question: How do we take a grown inside living cells and make it pure enough to safely put into a human body?Enduring understanding: A medicine is only as safe as it is pure, because whatever rides along with the target protein gets injected into the patient too.
Where you are · this course
GFP, chromatography, SDS-PAGE / gel interpretation, purity and QC. Purification overview ▸ Day 1
Day 69 of 72 this semester3 left before WebXam
🧬 Where you are · PLTW
Medical InterventionsUnit 4: How to Prevail When Organs Fail ▸ Lesson 4.1 Manufacturing Human Proteins"Activity 4.1.3 Protein Purification"
Matched to your live myPLTW course (verified June 2026).
Today's driving question

If a batch of comes out of bacteria mixed with thousands of other bacterial proteins, DNA, and cell membrane pieces, what has to be removed before a person can inject it, and why?

Today you'll be able to

Explain why a manufactured must be purified and what means for a medicine.

You've got it when
  • You'll be able to explain why a medicine must be purified.
  • You'll be able to define and a risk of impurity.
Due today · Exit ticket RequiredShort exit ticket defining and identifying one concrete risk of an impure medicine.
Do-Now · start these with your notes closed
  1. When bacteria are grown to make a human , name two things besides the target protein that end up in the mixture when the cells are broken open.
  2. Why might a patient's body react badly to a medicine that still has bacterial leftovers in it?
Do this · step by step
numbered so we can always find our place
  1. 1Read the overview notes in the PLTW course shell and define .
  2. 2List what else is in the cell mixture besides the target .
  3. 3Explain why an impure medicine could be unsafe.
  4. 4Preview the steps you will model this week.
  5. 5Submit a short exit ticket defining and one risk of impurity.
Interrupted or lost? Pick up at the notes: define as the ratio of target to total protein, then finish your exit ticket with one definition of purity and one risk of impurity.
Optional project open: 072130 Molecular Lab Review - solo or group, about 1.5 to 2 hours total. Due by Fri, Jan 15, 2027. Great WebXam prep.

🛠 Get unstuck · pick your level

Need a running start
Think of straining pasta: the noodles are what you want, the water is everything else. Today the target protein is the noodles and the bacterial soup is the water we have to drain away.
On track
Explain purity as the ratio of target protein to total protein, and give one concrete reason an impure protein injection could harm a patient.
Stuck? Get unstuck
Start with a single sentence: a protein medicine has to be pure because everything mixed in with it gets injected too. Then list two contaminants from the cell mixture and why each is a problem.
Push me further
Real biologics are never 100 percent pure. Argue what purity threshold you would set for an injected drug versus a topical one, and defend the number with the immune risk.

🔑 Today's words · 5

GFPchromatographyelutionprotein markerpurity
+1 more in the word bank

Tap a word in the lesson for a plain meaning and one example. Recycled into next week's Do-Now.

Today's study notebook
Purifying proteins: chromatography, SDS-PAGE, and separating a protein of interest.
Open the notebook
Audio overviewVideo overviewMind mapStudy guideFlashcardsQuizData table
Where this fits
Tested on (Ohio WebXam)
Genetics of Disease · 072130
PLTW lesson
MI · Lesson 4.1 Manufacturing Human Proteins
WebXam domain
Bio-Molecular Technology
Evidence to produce
Exit ticket
Lab / skill
Genetic Science Learning Center: Genetics basics and proteins
Do the work · 80-minute blockfirst 5 min = hook

💡 Big idea: A manufactured must be purified because every contaminant left in the mixture gets injected into the patient and can trigger an immune reaction or weaken the drug.

  1. 0-10Read overview; define in own words
  2. 10-25List cell-lysate components besides target
  3. 25-42Explain risk of each contaminant type
  4. 42-58Preview this week's steps (, SDS-PAGE)
  5. 58-70Write exit ticket: definition and one impurity risk
  6. 70-80Submit exit ticket; preview Tuesday diagram
Mr. Mendoza's 5-minute intro
  • Your bacteria made the recombinant , but it is swimming in a soup of thousands of other molecules.
  • Before it can enter a patient, everything else has to be removed.
  • Today you learn what is in that soup and why impurity is not just a quality problem but a problem.
  • and QC connect to the Lab SOPs domain of the 072130 WebXam.
Know by the end
  • Cell lysate contains the target mixed with thousands of other bacterial proteins, DNA, and membrane fragments.
  • Contaminants in a therapeutic can provoke dangerous immune responses in patients.
  • is quantified by the ratio of target to total protein, often confirmed by gel analysis.
Open this PLTW section today

GFP, chromatography, SDS-PAGE / gel interpretation, purity and QC. · overview

Day 1 of this lesson. Open this exact section in myPLTW (find it in Clever, Microsoft sign-in), then do the work below.

Do this: Open the - unit tracker in myPLTW for Activity 4.1.3 GFP Protein Purification and read the purification overview notes.

Complete

Mark the -overview entry complete and attach your exit ticket.

How far to get

Cloning unit should be fully closed; this overview opens the - unit.

Upload as evidence

Exit ticket defining and one impurity risk submitted to the course shell.

All PLTW activities are completed inside the PLTW course environment: this page only gives direction. Submit producibles on Schoology.

Today's PLTW tracker · fill in and submit

Check things off as you work, then submit. This tells Mr. Mendoza how you're doing so he can help the class. It does not replace turning in your producible on Schoology.

Use the code Mr. Mendoza gave you, not your name. Saved on this device.

GFP, chromatography, SDS-PAGE / gel interpretation, purity and QC.Day 1 of this projectSee the full week plan
Today's PLTW target

GFP, chromatography, SDS-PAGE / gel interpretation, purity and QC. · Purification overview

Open the - unit tracker in myPLTW for Activity 4.1.3 GFP Protein Purification and read the purification overview notes.

Cloning unit should be fully closed; this overview opens the - unit.

This is how Mr. Mendoza sees the class keeping pace with PLTW. Be honest, it only helps if it is accurate.

1 · What you do today

🎯 Explain why a manufactured must be purified and what means for a medicine.

  • Read the overview notes in the PLTW course shell and define .
  • List what else is in the cell mixture besides the target .
  • Explain why an impure medicine could be unsafe.
  • Preview the steps you will model this week.
  • Submit a short exit ticket defining and one risk of impurity.
2 · What you turn in

Exit ticket: Short exit ticket defining and identifying one concrete risk of an impure medicine.

Turn it in on Schoology using the checklist just below. Upload by 11:29 PM for full credit.

3 · Who's doing what (team)
TaskWho
Read the overview notes in the PLTW course shell and define ._______
List what else is in the cell mixture besides the target ._______
Explain why an impure medicine could be unsafe._______
Preview the steps you will model this week._______
Submit a short exit ticket defining and one risk of impurity._______

Working solo? Put your own name in "Who" for every row.

4 · Words I can use correctly
5 · I'm successful today when I can…
  • You'll be able to explain why a medicine must be purified.
  • You'll be able to define and a risk of impurity.
6 · Reflection & next steps
Where are you today?0/7 checked
Pick your period and code first.
Your 4 steps today
  1. 1
    Do this
    Explain why a manufactured protein must be purified and what purity means for a medicine.
  2. 2
  3. 3
    Submit this
    Exit ticket: Short exit ticket defining purity and identifying one concrete safety risk of an impure protein medicine.
  4. 4
    Submit it here
    1. 1Open Clever.
    2. 2Microsoft (district) sign-in.
    3. 3Schoology and myPLTW are both in Clever.
    Look for this assignment in Schoology: Genetics of Disease (Medical Interventions) › GFP, chromatography, SDS-PAGE / gel interpretation, purity and QC. › Exit ticket
    Open Schoology
Were you absent? Jump to the make-up plan
Learn it · deck, reading, and vocabulary
Three-tier teaching slide deck

Tier 1 is the time-boxed teacher set for the block; Tier 2 adds scaffolded vocabulary, examples, and a reading routine; Tier 3 extends into careers and current biomedical applications.

Generated from this lesson's canonical data with a red-team citation check.

Watch the trap

Students often think Students assume that if bacteria were engineered to make the target , the protein comes out clean because that is what the cells were told to produce.. The trap: The engineered is a tiny fraction of everything inside the cell. Breaking the cells open releases all of the bacterium's own proteins, DNA, and membranes at the same time, so the target starts out badly outnumbered and must be separated, not just harvested.

Worked example · a parallel case (guides, does not reveal)
Purity-and-impurity exit ticket
Completes: Completes the purification overview: a short exit ticket defining purity and naming one concrete safety risk of an impure protein medicine.

Definition of purity: purity is how much of the total protein in my sample is actually the target protein, rather than other proteins and cell parts. High purity means almost all of it is the protein I want.

What else is in the mixture: besides my target protein, the cell lysate contains thousands of other bacterial proteins, DNA, and broken membrane fragments.

One safety risk of impurity: if a protein medicine still contains bacterial contaminants, those contaminants can trigger a dangerous immune reaction in the patient, so an impure dose is not just less effective, it can be unsafe.

Also due today: Submit your exit ticket to the course shell before leaving class.

See the full worked example
Portal terms
CER:
Claim, Evidence, Reasoning: make a claim, back it with evidence, explain your reasoning.
SOP:
Standard Operating Procedure, the exact steps to follow (especially in a lab).
Tracker:
Your PLTW progress log where you record completed evidence.
myPLTW:
The PLTW course site where you do the online activities. Find it in Clever with your Microsoft sign-in, right next to Schoology.
This unit's vocabulary
(Green Fluorescent Protein)/kroh-muh-TOG-ruh-fee/(Quality Control)

Tap the speaker to hear a term. Add two of these to your notebook glossary with a definition and an example in your own words.

Build your vocabulary · optional, for extra credit

Pick just 2 or 3 words from today and make them yours: write what each one means in your own words, then give one example from what you actually did in Purification overview. Try your own words first; the glossary is there if you get stuck. This is voluntary and counts as extra credit, so keep it short.

GFP
chromatography
elution
protein marker
purity
QC

Saved on this device. Show Mr. Mendoza or add these to your notebook glossary to claim the extra credit.

Teacher-posted resources

Classroom documents for this lesson are posted in Schoology. Open Schoology and find each one by the name shown on its card.

Use during lessonFor: Everyone
Activity 4.1.3 Protein Purification (Chromatography)
worksheet/handoutPosted in Schoology
Open in Schoology

Open this when the class reaches this activity and use it to complete the required lesson artifact.

Placement rationale

Matched and quality control by path:Medical-Interventions/Unit-4_When-Organs-Fail/4.1_Manufacturing-Human-Proteins; keywords:protein purification, gfp, . Score 150. Visibility: student-schoology (student-facing resource; link through Schoology rather than local path).

Use during lessonFor: Everyone
4.1.3 Protein Purification by Column Chromatography Student Guide
worksheet/handoutPosted in Schoology
Open in Schoology

Open this when the class reaches this activity and use it to complete the required lesson artifact.

Placement rationale

Matched and quality control by path:Medical-Interventions/Unit-4_When-Organs-Fail/4.1_Manufacturing-Human-Proteins; keywords:protein purification, gfp, . Score 150. Visibility: student-schoology (student-facing resource; link through Schoology rather than local path).

Catch-up / reteachFor: Need extra support
GFP Purification Bio-Rad Quick Guide
worksheet/handoutPosted in Schoology
Open in Schoology

Use this if you were absent, got stuck, or need another pass before you submit the lesson artifact.

Placement rationale

Matched and quality control by path:Medical-Interventions/Unit-4_When-Organs-Fail/4.1_Manufacturing-Human-Proteins; keywords:gfp, . Score 142. Visibility: student-schoology (student-facing resource; link through Schoology rather than local path).

How to get there: open Clever and sign in with your Microsoft (district) account. You will find both Schoology and myPLTW right there in Clever. Turn in your work on Schoology; do the online activities in myPLTW.

Check yourself · commit, then reveal
Quick self-check · commit, then reveal

A lab reports their protein prep is '30 percent pure.' What does that number mean, and is it ready to inject?

How sure are you?

Write an answer and pick a confidence to unlock the key.

Cumulative WebXam review · flash practice

Fast retrieval with instant answers, not the commit-then-reveal check above. Try each from memory first: write what you remember about the earlier units, then check yourself here.

Tap an answer to check it · nothing is recorded or graded
[Review: Heat Maps and Hunches: Reading Gene Expression] On a microarray, a saturated YELLOW spot tells a scientist that the gene is
[Review: From Biopsy to Plan: Treating Cancer] A tumor suppressor gene that cannot correct damage will trigger apoptosis. Apoptosis is
[Review: Building a Gene Factory: Cloning Basics] Transformed bacteria are plated on agar containing an antibiotic because the plasmid also carries an antibiotic-resistance gene. This step
A single protein was denatured and run on a gel, producing four bands (two small and two large). What can you infer?
Go further and get help
Where this leads: careers

What today's skills lead to. These are real health-science careers this course builds toward. Tap one to see, on the US Department of Labor's O*NET site, what the job actually involves, what it pays, and how fast it is growing.

What to do if you were absent
If YOU are absent

Today is individual PLTW work, so do exactly what we did in class, from home: complete the same PLTW target above, then submit your Exit ticket.

Open Schoology (CMSD) and keep going

How to get there: open Clever and sign in with your Microsoft (district) account. You will find both Schoology and myPLTW right there in Clever. Turn in your work on Schoology; do the online activities in myPLTW.

If MR. MENDOZA is absent

Class still runs. Complete the online activity above (it's self-guided). Need the concept taught without a teacher? Use this authoritative explainer:

Genetic Science Learning Center: Genetics basics and proteins
Optional extra credit (async)

You've passed Unit 2, so the optional extra-credit track is open. Complete reserved-unit work from home (virtual labs included) for extra credit, submitted on Schoology.

Open the extra-credit track
How this is graded
For: Exit ticket: Short exit ticket defining purity and identifying one concrete safety risk of an impure protein medicine.
  • Complete
    Every required part of the artifact is present, nothing left blank.
  • Accurate
    The science and the data are correct and match the evidence.
  • Scientific reasoning
    You explain your claim with evidence and reasoning (CER), not just an answer.
  • Professional communication
    Clear, organized, labeled, and written the way a clinician or scientist would.
  • Submitted
    Turned in the right way (Schoology for routine work) and confirmed.